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Jatiphaladi Churna and Chitrakadi Gutika in the treatment of Grahani (Irritable bowel Syndrome)

Clinical Evaluation of Jatiphaladi Churna and Chitrakadi Gutika in the Management of Grahani

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/08/020607
Enrollment
100
Registered
2019-08-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K582- Mixed irritable bowel syndrome

Interventions

Intervention1: 1. Jatiphaladi Churna : Dose: 2gm twice daily Dosage form: Churna (powder) Route of Administration : Oral Time of Administration : Twice a day after food Anupana : Water Duration o

Sponsors

CCRASNew Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex aged 18-65 years 2. Known cases of Grahani (diagnostic criteria as per classical Ayurvedic Parameters) with following symptoms 3. Patients willing to give written informed consent and able to participate for 3 months.

Exclusion criteria

Exclusion criteria: 1. Patients with history of Inflammatory Bowel Disease (IBD), Kochâ??s Abdomen, Gluten Intolerance. 2. Patients with history of chronic amoebiasis. 3. Known cases of Diabetes Mellitus. 4. Patients with poorly controlled Hypertension ( >160/100 mmHg) 5. Patients who have history of Atrial Fibrillation, Acute Coronary Syndrome, Myocardial Infarction, Stroke or Severe Arrhythmia in the last 6 months 6. Symptomatic patients with clinical evidence of Heart failure 7. Known cases of malignancy 8. Patients with concurrent serious hepatic disorders (defined as Aspartate Amino Transferase (AST) and / or Alanine Amino Transferase (ALT) > 2 times upper normal limit) or Renal Disorders (defined as S. Creatinine >1.2mg/dL), Severe Pulmonary Dysfunction (uncontrolled Bronchial Asthma and / or Chronic Obstructive Pulmonary Disease (COPD). 9. Women who are planning for conception / pregnant or lactating. 10. H/o hypersensitivity to any of the trial drugs or their ingredients 11. Patients who have completed participation in any other clinical trial during the past three months 12. Any other condition which the Investigator thinks may jeopardize the study

Design outcomes

Primary

MeasureTime frame
To assess the clinical efficacy of Jatiphaladya Churna & Chitrakadi Gutika by the assessment of Changes in Ayurvedic Parameters of Grahani Timepoint: Base line , At the end of 14th day, 28th day, 42nd day, 56th day, and 70th day, 84th day and 98th day.

Secondary

MeasureTime frame
To assess the clinical efficacy of Jatiphaladya Churna & Chitrakadi Gutika by the assessment of Changes in IBS-QOL scoreTimepoint: Base line , At the end of 14th day, 28th day, 42nd day, 56th day, and 70th day, 84th day and 98th day.

Countries

India

Contacts

Public ContactDr Purnendu Panda

Centra Ayurveda Research Institute For Hepatobiliary Disorders, Bharatpur, Bhubaneswar

pandapurnendu02@yahoo.com06742387702

Outcome results

None listed

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