clinical study to evaluate the efficacy of vasa Pratisarniya kshar in the management of abhyantara arsha w.s.r internal haemorrhoid (1 st and 2nd degree)
Trial Snapshot
- Phase
- Phase 3
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 45
- Locations
- 1
- Primary Endpoint
- Reduction in size of pile mass
Study Overview
Brief Summary
Arsha can be defined as dilated plexus of superior haemorrhoidal veins,in relation to
anal canal.Due to indulgence in incompatible food,there is a diminution of agni leading to constipation and vegdharana which leads to pratilomgati of Apana vayu. There are several drugs for Arshas but here I have chosen Pratisarniya kshar which not only treat it’s symptoms but also does samprapti bhanga.
Therefore I have selected 45 patients aged between 30-60 years,patients should be selected on the basis of inclusion and exclusion criteria . The trial will be of 21 days or 3 weeks follow up will be done after every week. Cured after 3rd week patient gets 80-100 percent from sign and symptoms
Study Design
- Study Type
- Interventional
- Allocation
- Other
- Masking
- Not Applicable
Eligibility Criteria
- Ages
- 30.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients having Arsha who are fulfilling my study criteria and who are willing to be selected will be enrolled Patients with 1st and 2nd degree haemorrhoids Patient of the age group above 30 years – below 60 years Patient will be selected irrespective of sex Patients who will be ready to give written consent.
Exclusion Criteria
- •Patients planning to conceive in near future[during course of trial] Any congenital diseases like haemophillia Patients with 3 degree, 4 degree or prolapsed piles Pregnant women and Lactating mothers Patients suffering from Thrombosed Piles mass,Ulcerative Colitis and CA rectum.
Outcomes
Primary Outcomes
Reduction in size of pile mass
Time Frame: 21 days or 3 week | The trial drug will be given for 3 weeks and follow up will be done after 3rd week
Secondary Outcomes
- Bleeding reduced per rectum and relief in burning sensation(After analysing all the parameters the result will be assessed on the basis of symptomatic relief and improvement.)