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Clinical Study of the Efficacy of Children's Dietary Supplement iKids-Growth in improving height development of children at risk for growth retardation

Clinical Study of the Efficacy of Children's Dietary Supplement iKids-Growth in improving height development of children at risk for growth retardation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091874
Enrollment
Unknown
Registered
2024-11-05
Start date
2024-11-05
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

at risk for growth retardation

Interventions

iKids-Growth intervention group:iKids-Growth
Control group:None

Sponsors

Shanghai Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1.Age 5-10 years, i.e. 5 years and above, under 11 years, excluding 11 years; 2.The height corresponding to the same sex and age is within the range of P3-P10; 3.The subject and/or guardian understand the purpose of the study, the possible risks and benefits of the study, agree to participate in the clinical study, and voluntarily sign the informed consent;

Exclusion criteria

Exclusion criteria: 1.Patients with abnormal blood glucose (fasting blood glucose =5.7mmol/L); 2.Undergoing growth hormone treatment; 3.Liver and kidney dysfunction (ALT> 1.5 times the upper limit of normal, Cr> the upper limit of normal). 4.Other diseases or factors causing growth disorders (growth hormone deficiency, attachment deprivation, Turner syndrome, Laron syndrome, skeletal dysplasia, etc.); 5.Patients who have used systemic or local hormone therapy (such as growth hormone, sex hormone, glucocorticoid, etc.) within 3 months and have received drug therapy that may interfere with GH secretion or GH effect (oxandrosterone, growth hormone-releasing hormone, etc.). 6.Subjects who are allergic to the dietary supplements used in this clinical trial. 7.Subjects who have participated in a drug clinical trial within the past 3 months. 8.Subjects whose guardians are with cognitive impairments. 9.Other conditions deemed unsuitable for inclusion in this clinical study by the investigator.

Design outcomes

Primary

MeasureTime frame
annual height velocity;the improvement of height SDS;

Secondary

MeasureTime frame
IGF-1 and IGFBP-3;Bone age;

Countries

China

Contacts

Public ContactJinjin Chen

Shanghai Children's Hospital

chenjj@shchildren.com.cn+86 21 52976152

Outcome results

None listed

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