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A study to evaluate the effect of giving Pre operative intramuscular injection diclofenac on post operative pain and use of opioids in patients posted for peri anal surgeries

A Randomised Controlled Study to Evaluate the effect of preoperative Intramuscular Diclofenae sodium on Duration of Postopreative Analgesia in Patients for Perianal surgeries Under saddle Block at SMS Medical College, Jaipur . - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091166
Enrollment
60
Registered
2025-07-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Inj. Diclofenac sodium 1mg/kg: Intramuscular Diclofenac sodium1mg/kg injection post operative Control Intervention1: 0.9%Normal saline 2ml: Intramuscular normal saline 0.9% 2ml injectio

Sponsors

SMS Medical College and Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients scheduled for elective perianal surgery under saddle block. 2.Patient willing to give informed written consent. 3.Age above 18 years, belonging to either sex. 4.American Society of Anaesthesiologist (ASA) physical status I and II.

Exclusion criteria

Exclusion criteria: 1.Patient should not be a part of any other study 2.Patients who have contraindications for regional anaesthesia 3.Patients with bleeding disorders. 4.Allergic to amide local anaesthetics. 5.Duration of surgery more than 30 minutes. 6.Patients with mental health problems.

Design outcomes

Primary

MeasureTime frame
1. To assess and compare the difference in the time to first rescue analgesic request in the first 24 hours postoperatively between the two groups. 2. To assess and compare the difference in rescue analgesic consumption between the two groups.Timepoint: 1. To assess and compare the difference in the time to first rescue analgesic request in the first 24 hours postoperatively between the two groups. 2. To assess and compare the difference in rescue analgesic consumption between the two groups.

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDivya agrawal

SMS Medical College Attached Hospitals Jaipur Rajasthan

Dadivyaagrawal02@gmail.com8529493218

Outcome results

None listed

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