Randomized Controlled Clinical Trial To Study The Efficacy Of Jyotishmati Beeja Kalka Lepa In The Management Of Raktarsha With Special Reference To I And II Degree Internal Haemorrhoids.
Overview
- Phase
- Phase 2/3
- Status
- Not yet recruiting
- Sponsor
- LRP Ayurvedic Hospital And Research Centre
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- To Study The Efficacy Of Jyotishmati Beeja Kalka Lepa In The Management Of Raktarsha With Special Reference To I And II Degree Internal Haemorrhoids
Overview
Brief Summary
This is Randomized Controlled Clinical trial to study the efficacy of Jyotishmati Beeja Kalka Lepa In the management of Raktarsha with special reference to I and II degree Internal Haemorrhoids. Jyotishmati beeja kalka lepa and haridradi lepa both are antiinflammatery, vednasthapana, vatahara properities. the age group taken for study trail will be between 18-60 years .ayurvedic formalation will be given for 10 days and f/o after 15th and 20th days . evaluation of no PR bleed effect of both groups using statistical tools will be done and conclusion will be made.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- None
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •1.Patients age 18-60 years 2.Patients having fulfilling criteria for diagnosis of internal haemorrhoids such as PR bleeding I degree and II degree constipation protrusion of mass.
- •3.Patients will be selected irrespective of sex and socioeconomic status and religion.
Exclusion Criteria
- •1.External thrombosed and strangulated haemorrhoids III and IV degree.
- •2.Haemorrhoids associated with fissure,fistula-in- ano,malignancy of rectum and anal canal rectum prolapsed,CA prostate,peptic ulcers,AIDS Kochs,liver disease,liver cirrhosis.
- •3.Pregnant and lactating women.
Outcomes
Primary Outcomes
To Study The Efficacy Of Jyotishmati Beeja Kalka Lepa In The Management Of Raktarsha With Special Reference To I And II Degree Internal Haemorrhoids
Time Frame: 10 days
Secondary Outcomes
- To study the effect of ayurvedic formulation(10 days with f/o after 15th and 20th days)
Investigators
Dr Sweety Rushi Undirwade
LRP Ayurvedic Medical College And Hospital