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Clinical Evaluation of Hingwashtaka Churna and ayurvedic panchakarma procedure with Dietary Correction in Children with Functional Constipation.

Efficacy of Hingwashtaka Churna and Bala Taila Matra Basti along with Dietary Corrections in the management of Vibandha w.s.r. to Functional Constipation in Children An open labelled single arm clinical trial. - nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110990
Enrollment
30
Registered
2026-05-25
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: K590- Constipation

Interventions

None listed

Sponsors

Institute of teaching and research in ayurveda Jamnagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The children of either gender between the age group of 2-14 years. Who must fulfill at least 2 criteria from the Diagnostic Criteria for functional constipation. Patients of constipation whose parents are willing to give the consent.

Exclusion criteria

Exclusion criteria: 1.The children age less than 2 years and more than 14 years. 2.Children having constipation secondary to any of the other diseases like Cerebral palsy, Autism, Hypothyroidism, Hirschprung disease and structural anomalies of Anal Canal, Irritable bowel movement will be excluded from the trial based on clinical presentations. 3.Children having any systemic illness and recent Abdominal surgeries. 4.Children on drugs like Opiates, Anticholinergic agents, Phenobarbitone etc

Design outcomes

Primary

MeasureTime frame
Improvement in sign and symptoms of Vibandha (Functional Constipation) assessment by subjective parameters scale Wexner constipation scoring system The total effect of treatment will be assessed in the term of complete remission, marked improvement, moderate improvement, mild improvement and no changes. Timepoint: patient will be assessed on day 1 and day 28. Total duration of intervention is 28 days.

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactDr Apex G Vyas

Institute of teaching and research in ayurveda jamnagar

dr_apexa_r@yahoo.com08815701586

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026