"It is a study to see Effectiveness of Kshudrasevantika taila pichu and Doorvadi taila pichu in the management of Parikartika With Special Reference to Fissure in Ano"

Phase 3

Not yet recruiting

• Conditions: Disease of digestive system, unspecified. Ayurveda Condition: PARIKARTIKA, (2) ICD-10 Condition: K928||Other specified diseases of the digestive system. Ayurveda Condition: PARIKARTIKA,

• Registration Number: CTRI/2023/01/048884
• Lead Sponsor: BLDEAS AVS Ayurveda Mahavidyalaya

Brief Summary

This study is randomized comparative clinical study to evaluate the efficacy of kshudrasevantika taila pichu over doorvadi taila pichu in the management of parikartika with special reference to acute fissure in ano that will be conducted  in BLDEAS AVS Ayurveda Mahavidyalaya, hospital and research centre, vijayapura - 586106 karnataka, india

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2023-10-01
• Study Start: 2023-12-01

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Patient having classical features of acute fissure-in-Ano namely a longitudinal ulcer in the anal region with any one or more of the following features: Excruciating pain in anal region during and after defecation,bleeding per anum,Constipation,burning sensation and presence of sphincter spasm will beselected acute solitary fissure patients of age group18-80 years of bothe gender.

Exclusion Criteria

• 1.Patients with K/C/O Ulcerative colitis, Syphilis, Crohn’s disease, inflammatory bowel disease and other systemic disease pertaining to rectum and anal canal will be excluded from the study.
• 2.Acute multiple fissures will be excluded from the study.
• 3.Patient with chronic fissure in ano,ca of rectum,ca of anal canal, fistula in ano, hemorrhoids or any other ano-rectal diseases.
• 4.Patient with systemic disorders such as diabetes, tuberculosis.
• 5.HIV, HBsAg& HCV positive patients.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduce in pain,burning sensation,bleeding per rectum and consitation	21 days

Secondary Outcome Measures

Name	Time	Method
Reduction in ulcer size, improvement in the wound healing	21 days

Trial Locations

Locations (1)

BLDEAs AVS Ayurveda Hospital,Vijayapura; 🇮🇳 Bijapur, KARNATAKA, India

BLDEAs AVS Ayurveda Hospital,Vijayapura

🇮🇳Bijapur, KARNATAKA, India

Diksha Parmar

Principal investigator

9380174080

dikshaparmar82@gmail.com