To Study The Rujahar Effect Of Patha- Yavasa Churna In The Management Of Arsha.

Phase 2/3

Not yet recruiting

• Conditions: Other specified diseases of the digestive system. Ayurveda Condition: ARSAH,

• Registration Number: CTRI/2025/05/086546
• Lead Sponsor: Dr Monali Yesulal Uprade

Brief Summary

This is single arm Clinical trial to study the effect of Patha- Yavasa churna in the management of arsha with special reference to Haemorrhoids.

Patha - Yavasa churna both are antiinflammatery, vednasthapana, vatahara and raktasthambhana properities.

the age group taken for study trail will be between 18-60 years.

ayurvedic formulation will be given for 7 days and f/o after 10th day.

Evaluation of rujahar effect of both groups using statistical tools will be done and conclusion will be made.

Detailed Description

Not available

Study Timeline

• Study Start: 2025-05-20
• Last Update Posted: 2025-07-05

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• 1.Patients Age.
• 18 to 60 years. 2.Patients having fulfilling criteria for diagnosis of internal haemorrhoids such as pain, PR Bleeding, constipation, Protrution of mass. 3.Patient will be selected irrespective of Sex and socioeconomic status and religion.

Exclusion Criteria

• 1.Pateint below age 18 year and above 60 years.
• 2.External, Thrombosed & strangulated Haemorrhoids..
• 3.Haemorrhoids associated with fissure in-ano,fistula in-ano, malignancy of rectum and anal canal, rectal prolapsed, etc.
• CA prostate, peptic ulcers, AIDS, Koch’s, liver disease, liver cirrhosis.
• 4.Pregnant and lactating women.
• 5.Systemic disorders such as DM, Anemia, bleeding disorder (Coagulopathy), HTN.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To study the rujahar effect of patha - yavasa choorna in the management of arsha with special reference to haemorrhoid .	7 days

Secondary Outcome Measures

Name	Time	Method
To study the effect of ayurvedic formulation.	7 days with f/u after 10 days.

Trial Locations

Locations (1)

SMBT College And Hospital; 🇮🇳 Nashik, MAHARASHTRA, India

SMBT College And Hospital

🇮🇳Nashik, MAHARASHTRA, India

Dr Monali Yesulal Uprade

Principal investigator

07028786195

monaliuprade31@gmail.com