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Efficacy and Safety of Tenoten for Children in the Treatment of Specific Developmental Disorders of Scholastic Skills in Children

Multicenter Double-blind Placebo-Controlled Randomized Clinical Trial of Efficacy and Safety of Tenoten for Children in the Treatment of Specific Developmental Disorders of Scholastic Skills in Children

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03159104
Enrollment
240
Registered
2017-05-18
Start date
2015-08-25
Completion date
2019-02-18
Last updated
2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Specific Developmental Disorders of Scholastic Skills

Brief summary

Purpose of the study: • To evaluate efficacy and safety of Tenoten for children in the treatment of specific developmental disorders of scholastic skills in children.

Detailed description

A multicenter, double-blind, randomized, placebo-controlled clinical trial to evaluate the efficacy and safety of the study treatment. The study will enroll the school children (boys and girls) of grades 1, 2 and 3 of a regular school aged 7-9 years old (grade 1 school children will be enrolled at the beginning of the second half of the year) complaining of difficult learning classified according to ICD-10 as specific developmental disorders of scholastic skills (F81) including: * specific reading disorder (F81.0); * specific spelling disorder (F81.1); * specific disorder of arithmetical skills (F81.2); * mixed disorder of scholastic skills (F81.3); * disorder simultaneously meeting criteria of F81.2+F81.0 or F81.2+F81.1, or F81.2+F81.0+F81.1. The developmental disorders of scholastic skills will be verified by a doctor (either a neurologist or psychiatrist) according to reading, spelling, and counting tests. The children may have any concomitant diseases not considered as exclusion criteria and not requiring therapy during the following 12 weeks using the products specified in section Forbidden concomitant therapy. Specific additional educational programs should not be performed within 12 weeks after enrollment either. On signing information sheet (informed consent form) by the parent/adopter the patients will be examined by a neurologist or psychiatrist and tested for reading skills (method by L.A. Fotekova, Т.V. Akhutina, 2002;), spelling skills (method by L.A. Fotekova, Т.V. Akhutina, 2002) and counting skills (subtest No. 3 Arithmetic WISC test), and concomitant therapy will be recorded. If inclusion criteria are met and non-inclusion criteria are absent at Visit 1, the patient will be enrolled in the trial and randomized into one of the two groups: 1 tablet of Tenoten for children three times daily for 3 months (group 1) or the same dosing regimen of Placebo (group 2). At Visit 1 the parents/adopters will receive the study product for 12-week treatment period and a diary to report any potential adverse events and cases of concomitant therapy. Six weeks later (Week 6±3 days) a Phone visit (Visit 2) will be made in order to interview parents about the patient's condition, the presence/absence of concomitant diseases, adverse events. At Visit 3 (Week 12±3 days) repeated testing of reading, spelling and counting skills will be made, complaints, data on concomitant diseases, concomitant therapy, and adverse events will be collected. The investigator will evaluate the subject's compliance and fill in the Clinical Global Impression Scale to calculate Efficacy Index (CGI-EI). The patients will be allowed to take symptomatic therapy and medications for their co-morbidities during the study, except for the medicines listed in Forbidden concomitant therapy.

Interventions

Tablet for oral use.

DRUGPlacebo

Tablet for oral use.

Sponsors

Materia Medica Holding
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
7 Years to 9 Years
Healthy volunteers
No

Inclusion criteria

1. Children of either gender aged 7 to 9 years old. 2. School children of grades 1-3 (grade 1 children will be enrolled at the beginning of the second half of the year) in regular schools with state accreditation with principal educational program of elementary general education in compliance with Federal State Educational Standard of the Russian Federation. 3. Beginning of the second half of the year (only for 1st grades). 4. Specific developmental disorder of scholastic skills such as: * specific reading disorder (F81.0); * specific spelling disorder (F81.1); * specific disorder of arithmetical skills (F81.2); * mixed disorder of scholastic skills (F81.3; i.e. meeting the criteria for one of the following combinations: F81.2+F81.0, F81.2+F81.1, or F81.2+F81.0+F81.1). 5. Reading score of 15 to 35 on the Reading Skills test (L.A. Fotekova, T.V. Akhutina, 2002). 6. Spelling score of 15 to 30 on the Spelling Skills test (L.A. Fotekova, T.V. Akhutina, 2002). 7. Counting score of 5 to 15 on subtest No. 3 Arithmetic (of Wechsler Intelligence Scale for Children). 8. Availability of a patient information sheet (Informed Consent form) signed by the parent/adopter to confirm the child's participation in the clinical trial.

Exclusion criteria

1. History of the diseases: * Diseases of the nervous system, including * inflammatory diseases of the central nervous system; * systemic atrophies; * extrapyramidal and movement disorders; * degenerative diseases of the nervous system; * demyelinating diseases of the central nervous system; * episodic and paroxysmal disorders; * polyneuropathies; * diseases of myoneural junction and muscle; * cerebral palsy. * Congenital malformations of the nervous system (excl. Spina bifida without hydrocephalus) * Diseases and congenital malformations of the eye causing impairment of vision. * Diseases and congenital malformations of the ear causing impairment of hearing. * Organic mental disorders. * Mental retardation ranging from mild to profound. * Stuttering (stammering). * Obsessive-compulsive disorder. * Pervasive developmental disorders including: * childhood autism; * atypical autism; * Rett syndrome; * overactive disorder associated with mental retardation and stereotyped movements; * Asperger syndrome. * Phakomatoses (tuberous sclerosis, neurofibromatosis). * Postconcussional syndrome. * Hereditary metabolic diseases, including glycogen storage disease (glycogenosis), disorders of galactose metabolism (galactosemia), other disorders of carbohydrate metabolism, disorders of glycosaminoglycan metabolism (mucopolysaccharidoses), disorders of aromatic amino-acid metabolism (phenylketonuria, tyrosinemia, etc.), disorders of branched-chain amino-acid metabolism and fatty-acid metabolism (maple-syrup-urine disease), mitochondrial myopathy. * Chromosomal abnormalities. 2. Administration of the products specified in section Forbidden concomitant therapy within the previous 4 weeks. 3. Necessity in pharmacotherapy for underlying and/or concomitant disease during the following 12 weeks. 4. Acute infectious disease or exacerbation/decompensation of a disease affecting the patient's ability to participate in the trial. 5. Malignant neoplasm/suspected malignant neoplasm. 6. Allergy/intolerance to any of the components of medications used in the treatment. 7. Malabsorption syndrome including congenital or acquired lactase deficiency (or another disaccharidase deficiency), and galactosemia. 8. Mental disorders of patient's parent(s)/adopter(s). 9. Use of drugs or alcohol by the patient's parents/adopters at \> 2 alcohol units a day (1 unit of alcohol is equivalent to 0.33 L of lager/150 mL of unfortified wine, or 40 mL of Ethyl Alcohol). 10. Participation in other clinical trials in the previous 3 months. 11. Patients whose parent(s)/adopter(s), from the investigator's point of view, will fail to comply with the observation requirements of the trial or with the dose regimen of the investigational drug. 12. Patients whose parent(s)/adopter(s) are related to any of the on-site research personnel directly involved in the conduct of the trial or are an immediate relative of the study investigator. Immediate relative means husband, wife, parent, son, daughter, brother, or sister (regardless of whether they are natural or adopted). 13. Patients whose parent(s)/adopter(s) work for OOO NPF MATERIA MEDICA HOLDING (i.e., is the company's employee, temporary contract worker, or, designated officials responsible for carrying out the research or any immediate relatives of the aforementioned).

Design outcomes

Primary

MeasureTime frameDescription
Mean Total Scholastic Skills Score (a Sum of Three Scales: Reading, Spelling, and Counting).On Day 1 and after 12 weeks of the therapyThe total scholastic skill score is calculated based on the points for reading, spelling, and counting skills. Reading skills are estimated according to scale consisting of three subscales:reading speed, reading method/understanding, and reading accuracy. The minimum value of reading skills scale is 0 points, and the maximum value is 45 points. Spelling skills are estimated according to scale in 0, 15, 30, and 45 points. The minimum value is 0 points, and the maximum value is 45 points. Counting skills are estimated according to subtest No. 3 Arithmetic of Wechsler Intelligence Scale for Children (WISC) in points. The minimum value is 0 points, and the maximum value is 20 points. Total scholastic skill score is a sum of three scales (reading, spelling, and counting). The minimum value is 0 points, and the maximum value is 110 points. A higher score means the best results.

Secondary

MeasureTime frameDescription
Mean Reading Skills ScoreOn Day 1 and after 12 weeks of the therapyReading skills are estimated according to scale consisting of three subscales: reading speed, reading method/understanding, and reading accuracy. Students of 7 years old are invited to read the words, and students of 8-9 years old are invited to read a small text. Speed, method, and accuracy of the reading are estimated in students of 7 years old. Speed, accuracy, and understanding of the text are estimated in students of 8-9 years old. The minimum value is 0 points, and the maximum value is 45 points. A higher score meant the best results.
Mean Score Spelling Skills ScoreOn Day 1 and after 12 weeks of the therapySpelling skills are estimated according to scale in 0, 15, 30, and 45 points. Students of 7 years old are invited to write dictated letters, their names, and three words (mom, table, trunk), and students of 8-9 years old are invited to write a small dictation. Dysgraphic errors and their types as well as the number of non-dysgraphic errors are taken into consideration for estimation. The minimum value is 0 points, and the maximum value is 45 points. A higher score meant the best results.
Mean Counting Skills Score.On Day 1 and after 12 weeks of the therapyCounting skills are estimated according to subtest No. 3 Arithmetic of Wechsler Intelligence Scale for Children (WISC) in points. Arithmetic subtest includes 16 tasks from elementary school arithmetic which are tackled verbally. Easiness of operating numbers, accuracy, and time spent on the tasks are estimated. Each task is rated in points (0 or 1), by the end of testing and rating for each task the sum of points (raw score) is calculated and converted into a scale score using standard tables. The minimum value is 0 points, and the maximum value is 20 points. A higher score meant the best results.
Percentage of Children With an Increase in Total Scholastic Skills Score (a Sum of Three Scales: Reading, Spelling, and Counting).On Day 1 and after 12 weeks of the therapyPercentage of children with an increase in total scholastic skills score (a sum of three scales: reading, spelling, and counting). Total scholastic skill score is a sum of three scales (reading, spelling, and counting). The minimum value is 0 points, and the maximum value is 110 points. A higher score meant the best results. The increase in total scholastic skills score means an increasing by at least 5 points compared to baseline.
Efficacy Index According to Clinical Global Impression Scale.In 12 weeks of the treatment.The Clinical Global Impression-Efficiency Index (CGI-E) scale consists of two subscales. Efficacy subscale measures efficacy of medicine based on the severity of symptoms at the end of therapy. The minimum value is 1 points, and the maximum value is 4 points. A higher score means the best results. Side effects subscale measures side effects of the medicine. The minimum value is 1 points, and the maximum value is 4 points. A higher score means the best results. The scale is filled in by the doctor at the final visit after 12 weeks of the treatment. In accordance with the results of treatment, the doctor expresses his opinion about the efficacy of the therapy and the degree of medicine safety, making marks in the appropriate columns of the table. The efficacy index is determined as intersection of columns of indicators of efficacy and side effects in the table. The minimum value is 0.25 points, and the maximum value is 4 points. A higher score means the best results.

Countries

Russia

Participant flow

Participants by arm

ArmCount
Tenoten for Children
Dose per administration: 1 tablet. 1 tablet three times daily (3 tablets per day). The tablets should be held in the mouth until complete dissolution, without meal. Tenoten for children: Tablet for oral use.
121
Placebo
Dose per administration: 1 tablet. 1 tablet three times daily (3 tablets per day). The tablets should be held in the mouth until complete dissolution, without meal. Placebo: Tablet for oral use.
116
Total237

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyViolation of inclusion criteria12

Baseline characteristics

CharacteristicPlaceboTotalTenoten for Children
Age, Categorical
<=18 years
116 Participants237 Participants121 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
0 Participants0 Participants0 Participants
Age, Continuous8.6 years
STANDARD_DEVIATION 0.6
8.6 years
STANDARD_DEVIATION 0.7
8.5 years
STANDARD_DEVIATION 0.7
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
Russia
116 participants237 participants121 participants
Sex: Female, Male
Female
46 Participants95 Participants49 Participants
Sex: Female, Male
Male
70 Participants142 Participants72 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 1220 / 118
other
Total, other adverse events
42 / 12229 / 118
serious
Total, serious adverse events
0 / 1222 / 118

Outcome results

Primary

Mean Total Scholastic Skills Score (a Sum of Three Scales: Reading, Spelling, and Counting).

The total scholastic skill score is calculated based on the points for reading, spelling, and counting skills. Reading skills are estimated according to scale consisting of three subscales:reading speed, reading method/understanding, and reading accuracy. The minimum value of reading skills scale is 0 points, and the maximum value is 45 points. Spelling skills are estimated according to scale in 0, 15, 30, and 45 points. The minimum value is 0 points, and the maximum value is 45 points. Counting skills are estimated according to subtest No. 3 Arithmetic of Wechsler Intelligence Scale for Children (WISC) in points. The minimum value is 0 points, and the maximum value is 20 points. Total scholastic skill score is a sum of three scales (reading, spelling, and counting). The minimum value is 0 points, and the maximum value is 110 points. A higher score means the best results.

Time frame: On Day 1 and after 12 weeks of the therapy

ArmMeasureGroupValue (MEAN)Dispersion
Tenoten for ChildrenMean Total Scholastic Skills Score (a Sum of Three Scales: Reading, Spelling, and Counting).Baseline61.39 score on a scaleStandard Deviation 12.04
Tenoten for ChildrenMean Total Scholastic Skills Score (a Sum of Three Scales: Reading, Spelling, and Counting).After 12 weeks79.94 score on a scaleStandard Deviation 18.22
PlaceboMean Total Scholastic Skills Score (a Sum of Three Scales: Reading, Spelling, and Counting).After 12 weeks74.56 score on a scaleStandard Deviation 18.75
PlaceboMean Total Scholastic Skills Score (a Sum of Three Scales: Reading, Spelling, and Counting).Baseline60.46 score on a scaleStandard Deviation 11.04
Comparison: The difference between final and initial total scholastic skill score was calculated for each participant. Wilcoxon test was used for comparison of these differences because data distribution differs from normal.p-value: 0.011395% CI: [1, 9]Wilcoxon (Mann-Whitney)
Secondary

Efficacy Index According to Clinical Global Impression Scale.

The Clinical Global Impression-Efficiency Index (CGI-E) scale consists of two subscales. Efficacy subscale measures efficacy of medicine based on the severity of symptoms at the end of therapy. The minimum value is 1 points, and the maximum value is 4 points. A higher score means the best results. Side effects subscale measures side effects of the medicine. The minimum value is 1 points, and the maximum value is 4 points. A higher score means the best results. The scale is filled in by the doctor at the final visit after 12 weeks of the treatment. In accordance with the results of treatment, the doctor expresses his opinion about the efficacy of the therapy and the degree of medicine safety, making marks in the appropriate columns of the table. The efficacy index is determined as intersection of columns of indicators of efficacy and side effects in the table. The minimum value is 0.25 points, and the maximum value is 4 points. A higher score means the best results.

Time frame: In 12 weeks of the treatment.

Population: The number of patients who have data on the CGI-EI scale is indicated.

ArmMeasureValue (MEAN)Dispersion
Tenoten for ChildrenEfficacy Index According to Clinical Global Impression Scale.2.36 score on a scaleStandard Deviation 0.87
PlaceboEfficacy Index According to Clinical Global Impression Scale.1.98 score on a scaleStandard Deviation 0.83
p-value: 0.0012Wilcoxon (Mann-Whitney)
Secondary

Mean Counting Skills Score.

Counting skills are estimated according to subtest No. 3 Arithmetic of Wechsler Intelligence Scale for Children (WISC) in points. Arithmetic subtest includes 16 tasks from elementary school arithmetic which are tackled verbally. Easiness of operating numbers, accuracy, and time spent on the tasks are estimated. Each task is rated in points (0 or 1), by the end of testing and rating for each task the sum of points (raw score) is calculated and converted into a scale score using standard tables. The minimum value is 0 points, and the maximum value is 20 points. A higher score meant the best results.

Time frame: On Day 1 and after 12 weeks of the therapy

ArmMeasureGroupValue (MEAN)Dispersion
Tenoten for ChildrenMean Counting Skills Score.Baseline11.14 score on a scaleStandard Deviation 2.24
Tenoten for ChildrenMean Counting Skills Score.After 12 weeks12.26 score on a scaleStandard Deviation 2.8
PlaceboMean Counting Skills Score.Baseline11.10 score on a scaleStandard Deviation 2.27
PlaceboMean Counting Skills Score.After 12 weeks11.80 score on a scaleStandard Deviation 2.73
p-value: 0.239195% CI: [0, 1]Wilcoxon (Mann-Whitney)
Secondary

Mean Reading Skills Score

Reading skills are estimated according to scale consisting of three subscales: reading speed, reading method/understanding, and reading accuracy. Students of 7 years old are invited to read the words, and students of 8-9 years old are invited to read a small text. Speed, method, and accuracy of the reading are estimated in students of 7 years old. Speed, accuracy, and understanding of the text are estimated in students of 8-9 years old. The minimum value is 0 points, and the maximum value is 45 points. A higher score meant the best results.

Time frame: On Day 1 and after 12 weeks of the therapy

ArmMeasureGroupValue (MEAN)Dispersion
Tenoten for ChildrenMean Reading Skills ScoreBaseline27.69 score on a scaleStandard Deviation 6.52
Tenoten for ChildrenMean Reading Skills ScoreAfter 12 weeks34.96 score on a scaleStandard Deviation 6.66
PlaceboMean Reading Skills ScoreBaseline27.76 score on a scaleStandard Deviation 6.16
PlaceboMean Reading Skills ScoreAfter 12 weeks33.66 score on a scaleStandard Deviation 7.7
p-value: 0.060895% CI: [0, 5]Wilcoxon (Mann-Whitney)
Secondary

Mean Score Spelling Skills Score

Spelling skills are estimated according to scale in 0, 15, 30, and 45 points. Students of 7 years old are invited to write dictated letters, their names, and three words (mom, table, trunk), and students of 8-9 years old are invited to write a small dictation. Dysgraphic errors and their types as well as the number of non-dysgraphic errors are taken into consideration for estimation. The minimum value is 0 points, and the maximum value is 45 points. A higher score meant the best results.

Time frame: On Day 1 and after 12 weeks of the therapy

ArmMeasureGroupValue (MEAN)Dispersion
Tenoten for ChildrenMean Score Spelling Skills ScoreBaseline22.56 score on a scaleStandard Deviation 7.53
Tenoten for ChildrenMean Score Spelling Skills ScoreAfter 12 weeks32.73 score on a scaleStandard Deviation 13.69
PlaceboMean Score Spelling Skills ScoreBaseline21.59 score on a scaleStandard Deviation 7.48
PlaceboMean Score Spelling Skills ScoreAfter 12 weeks29.09 score on a scaleStandard Deviation 14.58
p-value: 0.082495% CI: [0, 0]Wilcoxon (Mann-Whitney)
Secondary

Percentage of Children With an Increase in Total Scholastic Skills Score (a Sum of Three Scales: Reading, Spelling, and Counting).

Percentage of children with an increase in total scholastic skills score (a sum of three scales: reading, spelling, and counting). Total scholastic skill score is a sum of three scales (reading, spelling, and counting). The minimum value is 0 points, and the maximum value is 110 points. A higher score meant the best results. The increase in total scholastic skills score means an increasing by at least 5 points compared to baseline.

Time frame: On Day 1 and after 12 weeks of the therapy

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Tenoten for ChildrenPercentage of Children With an Increase in Total Scholastic Skills Score (a Sum of Three Scales: Reading, Spelling, and Counting).103 Participants
PlaceboPercentage of Children With an Increase in Total Scholastic Skills Score (a Sum of Three Scales: Reading, Spelling, and Counting).80 Participants
p-value: 0.0033Fisher Exact

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026