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Ayurveda management for indigestion in adults

Effect of an ayurvedic treatment protocol in the management of functional dyspepsia- A pre post test study. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085725
Enrollment
28
Registered
2025-04-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: K30- Functional dyspepsia

Interventions

None listed

Sponsors

Dr Manvi Singh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age 25 to 50 years of either gender 2.Participants fulfilling ROME IV diagnostic criteria. 3.Participants from whom the written consent is obtained.

Exclusion criteria

Exclusion criteria: 1.Participants who have been diagnosed with a gastrointestinal disease, as confirmed by esophagogastroduodenoscopy. 2.Participants who have obvious signs of irritable bowel syndrome. 3.Participants who have alarm symptoms (weight loss, black or tar stool, or dysphagia. 4.Participants who have a history of surgery associated with the gastrointestinal tract, except tor appendectomy, more than 6 months prior. 5.Women who are pregnant or breastfeeding. 6.Participants who are taking medication that may affect the gastrointestinal tract (a minimum washout period of 2 weeks is required before participating in the trial) (medications include NSAIDs, aspirin, prokinetic drugs, histamine-2 receptor antagonists, proton pump inhibitors, antidepressants, antibiotics, anti-ulcer drugs, absorbents, anti- flatulents, digestive drugs, anti-diarrheal , laxatives, antiemetics, emetics, anticholinergics, gastrin receptor antagonists, prostaglandin analogues , mucosal protective agents, steroids, and anticoagulants). 7.Participants who have uncontrolled chronic diseases (e.g., hypertension, diabetes mellitus) despite appropriate managements. 8.Participants who have a history of alcohol abuse or drug dependence.

Design outcomes

Primary

MeasureTime frame
SODA Score assessmentTimepoint: Oth day and 38th day

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Devipriya soman

Amrita school of ayurveda

priya3656@gmail.com9495638076

Outcome results

None listed

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