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Investigating the Effect of Intranasal Spray Containing Conditioned Medium from Umbilical Cord in Alzheimer's Disease

Safety of Intranasal Spray Containing the Conditioned Medium of Mesenchymal Stem Cells Derived from Umbilical Cord Wharton's jelly in Alzheimer's Disease (Mild to Moderate) in phase 1 of a clinical trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240131060870N1
Enrollment
9
Registered
2024-02-19
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Mild to moderate phase ,Alzheimer's patients, Alzheimer Disease, AD, Dementia. Diseases, Nervous System, Degenerative, Alzheimer's Disease, Late-onset, After the age of 65, AD, Dementia, Neurodegenerative, Central nervous system, CNS

Interventions

Intervention 1: Intervention group:: First, conditioned media solution or conditioned medium derived from mesenchymal stem cells from Wharton's jelly umbilical cord, 1 cc as an intranasal spray, twic

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients who have brain structural changes based on MRI and doctor's diagnosis, which confirms their Alzheimer's dementia. Gender and Age: men and women between 60 and 85 Y. Diagnosis of Mild to Moderate Alzheimer's dementia at least 6 months before the start of the study. MMSE (Mini-Mental State Examination) Score: 10 and 24 at the time of starting the study

Exclusion criteria

Exclusion criteria: Cancer patients who have been diagnosed in the last 5 years. Patients who cannot undergo MRI due to their condition. People with mental disorders Have diseases such as vitamin B12 deficiency, diabetes, hypo/hyperthyroidism, and hepatitis. History of cell therapy in the last 6 months. Subjects who have participated in another clinical study within 3 months before the start of this study. History of brain neoplasm.

Design outcomes

Primary

MeasureTime frame
Fever. Timepoint: Days 0, 1,2,3,4 and 2 weeks after CM (Conditioned Medium ) therapy. Method of measurement: Thermometer.;Headache. Timepoint: Days 0, 1,2,3,4 and 2 weeks after CM (Conditioned Medium ) therapy. Method of measurement: Visual Analogue Scale (VAS).;Dizziness, Nausea, and Vomiting. Timepoint: Days 0, 1,2,3,4 and 2 weeks after CM (Conditioned Medium ) therapy. Method of measurement: Dizziness Questionnaire: is a 25-item self-report questionnaire that quantifies the impact of dizziness on daily life by measuring self-perceived handicap. Item scores are summed. There is a maximum score of 100 (28 points for physical, 36 points for emotional and 36 points for functional) and a minimum score of 0.;Pro-inflammatory cytokines: IL-1ß, TNF-a and IL-6. Timepoint: Days 0, 1,2,3,4 and 2 weeks after CM (Conditioned Medium ) therapy. Method of measurement: Human interleukin ELISA kit: designed for quantitative measurement of ß1, IL-6 and TNF alpha in serum, plasma, cerebrospinal fluid and cell culture supernatant samples. This kit is designed and produced using monoclonal antibodies against human interleukins. Therefore, it is not used in measuring similar animal cases.;Growth Factors:GF:TGF-ß and BDNF. Timepoint: Days 0, 1,2,3,4 and 2 weeks after CM (Conditioned Medium ) therapy. Method of measurement: ELISA kit Human TGF-B and BDNF: designed to detect TGF-ß and BDNF in tissue samples, serum, plasma, cerebrospinal fluid and human cell culture supernatant.;Protein Amyloid beta (Aß). Timepoint: Days 0, 1,2,3,4 and 2 weeks after CM (Conditioned Medium ) therapy. Method of measurement: Blood Sample: Measurement of beta-amyloid plasma level by blood test.

Secondary

MeasureTime frame
The instrumental Activities of Daily Living Scale (IADL) is used to assess a patient's independent living skills and measures. Timepoint: 0 ,2 week,1 and 3 month after CM therapy. Method of measurement: IADL Paper Questionnaire: which has 18 points.;Montreal Cognitive Assessment Test (MOCA): was designed as a rapid screening tool for "mild cognitive impairment" and "Alzheimer's disease". Timepoint: 0 ,2 week,1 and 3 month after CM therapy. Method of measurement: MOCA Paper Questionnaire: It is used to measure different levels of memory and the person must have at least 6 classes of literacy.;Questionnaire ADL (Activities of Daily Living Scale) is a tool designed to measure the level of independence in ADLs in clinical outpatient populations. Timepoint: 0 ,2 week,1 and 3 month after CM therapy. Method of measurement: Questionnaire ADL is paper-based and has 14 points.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaser Amini

Iran University of Medical Sciences

amini.n@iums.ac.ir+98 21 8670 4720

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026