A clinical study to evaluate the efficacy of katphala caplet in post operative pain management in lower abdominal surgeries.

Randomised Controlled Clinical Study to evaluate the efficacy of katphala caplet with Diclofenac suppository in the management of post operative pain in lower abdominal surgeries. - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/06/088065

Enrollment

Registered

2025-06-02

Start date

Unknown

Completion date

Unknown

Last updated

2025-06-24

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

Conditions

Health Condition 1: Z488- Encounter for other specified postprocedural aftercare

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Post operative patient who have been operated for lower abdominal surgeries,inguino-scrotal surgeries,Ano-rectal surgeries, pelvic floor surgeries, genital surgeries

Exclusion criteria

Exclusion criteria: Patients who suffer from diarrhoea,acute fissure,active PR Bleeding,CA rectum,Tuberculosis of abdomen, dysentery

Design outcomes

Primary

Measure	Time frame
To study the efficacy of katphala caplet in post operative pain management as an analgesicTimepoint: 18 month	—

Secondary

Measure	Time frame
To compare the efficacy of katphala caplet with diclofenac suppositoryTimepoint: 18 month	—

Countries

India

Contacts

Public ContactDr Rashmi A Kale

MAMs Sumatibhai Shah Ayurved Mahavidhyalaya Malwadi Hadapsar Pune MAaharashtra 411028

drrakale@gmail.com9822244893

Outcome results