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Evaluate the efficacy of Bala Janma Ghuntika syrup in the management of abdominal colic in children.

A Pharmaceutical Evaluation of Bala Janma Ghuntika Sharkara and Its Therapeutic Effect On Udarashoola In Children - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/098971
Enrollment
60
Registered
2025-12-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: K929- Disease of digestive system, unspecified

Interventions

None listed

Sponsors

GOVERNMENT PG AYURVEDIC COLLEGE AND HOSPITAL,VARANASI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. FOR THIS STUDY, WE WILL CONSIDER CHILDREN BETWEEN 6 MONTHS TO 3 YEARS OF AGE WHO SHOW CLASSICAL UDARASHOOLA SYMPTOMS(KASHYAPA SAMHITA) THAT HAD BEEN LASTING FOR NOT MORE THAN 1 WEEK. 2. ALL GENDERS,CASTES,RELIGIONS AND SOCIOECONOMIC BACKGROUNDS ARE WELCOME, PROVIDED PARENTS/GUARDIANS GIVE CONSENT AND THE CHILD IS APPROPRIATE FOR OUTPATIENT OR CONSERVATIVE TREATMENT.

Exclusion criteria

Exclusion criteria: 1. PATIENTS OF AGE LESS THAN 6 MONTHS AND MORE THAN 3 YEARS AND WITHOUT THE SIGNS AND SYMPTOMS OF UADARASHOOLA WILL BE EXCLUDED FROM THE STUDY. 2. THE PATIENTS WITH ANY CONGENITAL ANOMALIES OR ANY INBORN ERRORS OF METABOLISM WILL BE EXCLUDED. 3. PATIENTS WITH KNOWN CASE OF VOLVULOUS,INTUSSCEPTION,DIVERTICULUM,INTESTINAL MALROTATION,ETC. AND OTHER SUCH EMERGENCY OR SURGICAL CASES WILL BE EXCLUDED.

Design outcomes

Primary

MeasureTime frame
RELIEF IN THE CLASSICAL SYMPTOMS OF UDARASHOOLA(KASHYAPA SAMHITA)Timepoint: 3rd day and 7th day

Secondary

MeasureTime frame
COMPLETE RELIEF FROM UDARASHOOLATimepoint: 14 DAYS

Countries

India

Contacts

Public ContactDR RUCHI TIWARI

GOVERNMENT PG AYURVEDIC COLLEGE AND HOSPITAL, VARANASI

dr.spandey2007@gmail.com9417077401

Outcome results

None listed

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