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A Clinical study to compare the effect of Palasa kshara bhavita Pippali and Rohithakadi choornam along with Phalatrikadi kwatha in patients of Gall Bladder stone.

A CLINICAL STUDY TO EVALUATE THE EFFECT OF PALASA KSHARA BHAVITA PIPPALI IN COMPARISON TO ROHITHAKADI CHOORNAM ALONG WITH PHALATRIKADI KWATHA IN CHRONIC CHOLELITHIASIS

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/11/029028
Enrollment
60
Registered
2020-11-10
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: K808- Other cholelithiasis

Interventions

Intervention1: Palasa Kshara bhavita Pippali: Palasa Kshara bhavita pippali choornam Capsule 500 mg BD for 30 days Control Intervention1: Rohithakadi Choornam with Phalatrikadi kwatha: Rohithakadi Cho

Sponsors

Central Council for Research in Ayurvedic Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with chronic cholelithiasis and chronic calculous cholecystitis Solitary or multiple stone & large stone measuring not > 1 cm

Exclusion criteria

Exclusion criteria: Age below 18 years and above 70 years Acute cholelithiasis Pregnant women GB CA Choledocolithiasis Large stone measuring >1 cm Known case of Tubercular Patients Malignancy HIV patients Hepatitis B patients Â

Design outcomes

Primary

MeasureTime frame
Size of Stone by USG GB Wall thickness by USGTimepoint: on 0th day and 31st day

Secondary

MeasureTime frame
FLATULENT DYSPEPSIA - DSAS score Timepoint: On 0th, 15th and 31st day;Pain Wong Baker scaleTimepoint: On 0th , 15th and 31st day;PRAKRTHI-TNMC 2004 QuetionnaireTimepoint: On 0th day;Tenderness-RUQTimepoint: On 0th, 15th and 31st day

Countries

India

Contacts

Public ContactDr Lakshman Singh

Banaras Hindu University

drlsingh@bhu.ac.in9415687065

Outcome results

None listed

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