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To evaluate the analgesic effect of patha nirgundi ghrita suppository in post operative pain in ano rectal surgeries

A Randomized Controlled Clinical Trial to Evaluate the Efficacy of Patha (Cissampelos pareira) Nirgundi (Vitex negundo) Ghrita suppository and Paracetamol Suppository in Post Operative Pain in Ano Rectal Surgeries - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/078922
Enrollment
60
Registered
2025-01-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: K929- Disease of digestive system, unspecified

Interventions

None listed

Sponsors

Dr Omkar Tukaram Khatkar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient experiencing pain post operatively in elective ano rectal surgeries

Exclusion criteria

Exclusion criteria: Patients having severe anemia ulcerative colitis crohns disease tuberculosis of the colon and rectum rectal prolapse and rectal cancer will be excluded in the trial

Design outcomes

Primary

MeasureTime frame
To study the Vednasthapan effect of patha nirgundi ghrita suppository in the post operative ano rectal surgeriesTimepoint: First dose of patha nirgundi ghrita suppository will be given on post operative day 0 and will be continue for 5 days and assessment will be done on post operative day 1 to day 5 and follow up after day 7.

Secondary

MeasureTime frame
To oberverd effect of Per rectal bleeding.Timepoint: First dose of patha nirgundi ghrita suppository will be given on post operative day 0 and will be continue for 5 days and assessment will be done on post operative day 1 to day 5 and follow up after day 7.

Countries

India

Contacts

Public ContactDr Amit A Paliwal

Dr D Y Patil College of Ayurved And Research Centre Pimpri Pune 18

dramitpaliwal@gmail.com8087975164

Outcome results

None listed

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