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Efficacy of RATADI VARTI (Suppository) in Post operative bowel evacuation and pain reduction in anorectal surgeries.

Efficacy of RATADI VARTI in Postoperative bowel evacuation and pain reduction in Anorectal surgeries- A Pre and Post test clinical study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/044497
Enrollment
30
Registered
2022-07-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: R194- Change in bowel habit Health Condition 2: R198- Other specified symptoms and signsinvolving the digestive system and abdomen

Interventions

None listed

Sponsors

Dr Archana Muraleedharan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients within 20-60 years irrespective of gender, religion and socio-economic status will be included. 2. Post-operative period less than 24hours. 3. Patients presenting with pain and constipation who underwent surgery for hemorrhoids, fistula-in-ano, fissure in ano. 4. Patients who have voluntarily agreed to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Ano rectal diseases associated with Tuberculosis. 2. Patients with increased serum IgE. 3. Patient not willing to undergo trial. 4. Patients with post-operative complications like severe bleeding

Design outcomes

Primary

MeasureTime frame
•Time duration of initiation of bowel evacuation after varti (suppository) insertion. •Frequency of bowel evacuation. Timepoint: Assessment done at 0th hour, after 1hr, 3hr and 6hr for 3days and time of initiation of bowel evacuation will be noted.

Secondary

MeasureTime frame
Post operative painTimepoint: Assessment done at 0th hour after 1 hour, 3 hour and 6 hour.

Countries

India

Contacts

Public ContactDr Rajeshwari P N

Amrita vishwa vidyapeetham

dr.rajeshwaripn@ay.amrita.edu8137070240

Outcome results

None listed

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