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A study to observe if probiotics supplementation is helpful in atopic dermatitis children

A randomised controlled study to evaluate the effectiveness of probiotics supplementation in the treatment of atopic dermatitis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/08/009236
Enrollment
114
Registered
2017-08-02
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patients of atopic dermatitis but who have chronic illness and are immunosuppressive are not recruited in the study.

Interventions

Intervention1: Probiotics supplementation: It is a randomised controlled trial with supplementation of the probiotics to one group of atopic dermatitis patients. Control Intervention1: Nil: This study

Sponsors

PGIMER Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Children with atopic dermatitis diagnosed according to Hanifin and Rajka between aged 6 months to 12 years. 2. All children in the above mentioned age group with be eligible irrespective of the disease severity.

Exclusion criteria

Exclusion criteria: 1. Immunocompromised chilren 2. Children with severe hepatic, renal or other systemic disease 3. 12 years of age

Design outcomes

Primary

MeasureTime frame
1. The mean difference in SCORAD in children with AD treated with conventional treatment plus probiotic supplementation versus conventional treatment alone at 0,12 and 24 weeks. 2. Mean difference in the number of days of treatment required to achieve 90% reduction in SCORAD in children with AD treated with conventional treatment plus probiotic supplementation versus conventional treatment alone. 3. Number of children with AD who relapse after stoppage of treatment at 24 weeksTimepoint: 0,12 and 24 weeks

Secondary

MeasureTime frame
1. To compare the IL-17 level in treatment vs control group at baseline and at 12 weeks 2. To compare the CDLQI and IDQOL at baseline and at 12 and 24 weeksTimepoint: 12, 24 weeks

Countries

India

Contacts

Public ContactRicha Sharma

Post Graduate Institute Of Medical Education And Research (PGIMER)

handa_sanjeev@yahoo.com9815924777

Outcome results

None listed

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