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Clinical Study on Palash Pushpa Churna In The Management of Grahani Roga

Phytochemical Study And Therapeutic Evaluation Of Palash Pushpa Churna In The Management Of Grahani Roga - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/081849
Enrollment
50
Registered
2025-03-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: K529- Noninfective gastroenteritis and colitis, unspecified

Interventions

None listed

Sponsors

Ayurvedic and Unani Tibbia college karol bagh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients between the age group of 21-60 years of age irrespective of sex Patints Willing and ready to sign the informed consent Patients suffering from symptoms of irritable bowel syndrome i.e. Muhu baddha drava Durgandhita Pichchhila Mal pravriti Aruchi Udara Shoola Vistambha Praseka Gaurava etc. over the past 3 months with symptom onset at least 6 months prior to diagnosis.

Exclusion criteria

Exclusion criteria: Patients having medical history of Intestinal Obstruction Crohns disease Ulcerative Colitis are excluded. Patients suffering from Acute diarrhoea Intestinal T.B. Gastric and Peptic ulcer uncontrolled D.M. and H.T. Gulma Arsha etc. Patients having any type of surgery or malignancyd Known case of serious hepatic cardiac or kidney diseases. Patients with known hypersensitivity to the trial drug. Patients on prolonged medication with corticosteroids antidepressants anticholinergics immunosuppressant etc. or any other drugs that may have an influence on the outcome of the study. Patients with poorly controlled hypertension systolic 140 and diastolic 90 mm of Hg despite of antihypertensive agents. Patients who have completed participation in any other clinical trial drugs ortheir ingredients.

Design outcomes

Primary

MeasureTime frame
The Expected Primary Outcome is improvement in the symptoms of grahani rogaTimepoint: At base line and 13 weeks

Secondary

MeasureTime frame
The Expected secondary outcome is the safety of the therapy under investigation. At the end of the study Safety of drug can be noted with any side effectTimepoint: 2 weeks & 13 weeks

Countries

India

Contacts

Public ContactDr Monika Tyagi

Ayurveda and Unani Tibbia College New Delhi

dr.monika0@gmail.com9354925054

Outcome results

None listed

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