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Role of Vikruta Kapha in Trupti as a Kaphaja Nanathmaja Vyadhi with special reference to symptoms of Functional dyspepsia and its management in children with Truptighna Mahakashaya

An interventional study to understand the role of Vikruta Kapha as a Kaphaja Nanathmaja vyadhi in causing Trupti (functional dyspepsia) in children and its management with Truptighna Mahakashaya - Trupti trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112793
Enrollment
30
Registered
2026-06-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

None listed

Interventions

None listed

Sponsors

Jammu Institute of Ayurveda and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: To obtain informed consent form for the trial from subjects belonging to the age group of 7-15 years. Subjects must have clinical signs and symptoms of anorexia and heartburn.

Exclusion criteria

Exclusion criteria: Subjects having any clinical condition or inability preventing from oral intake. Subjects having prior life-threatening conditions like Tuberculosis, Human Immuno Virus infection, Herpes simplex virus, Malignant carcinomas or any medical condition rendering the life expectancy less than 6 months.

Design outcomes

Primary

MeasureTime frame
In the primary outcomes we will be assessing subjective parameters (Kapha vruddhi lakshanas as per Acharya Charaka) with questionnaire such as PUSH score for skin health and wound healing, hair fall and others to prove the corresponding objectives.Timepoint: Assessments will be done pre- and post-intervention, that is on Day 1 Week 1 and on last day of intervention, that is on Week 5 respectively.

Secondary

MeasureTime frame
Secondary assessments will include Napean Dyspepsia Index & Patient Assessment of Upper Gastrointestinal Disorders-Symptom Severity Index scoring & their statistical analysis after the last day of intervention in Week 5.Timepoint: Assessments will be done on Day 1 Week 1 followed by last day of intervention on Week 5.

Countries

India

Contacts

Public ContactDr Hrishikesh S Acharya

JAMMU INSTITUTE OF AYURVEDA AND RESEARCH

hrishikeshacharya5@gmail.com6362277837

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026