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Clinical Trials/CTRI/2024/06/069307
CTRI/2024/06/069307
Not yet recruiting
Not Applicable

A comparative evaluation of ultrasound guided pudendal nerve block for postoperative analgesia in patients undergoing stapled hemorrhoidectomy.

Not provided1 site in 1 country70 target enrollmentStarted: July 1, 2024Last updated:
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Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
70
Locations
1
Primary Endpoint
Time of requirement of first rescue opioid analgesic.
OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Overview

Brief Summary

This is a clinical study designed to judge the efficacy of pudendal nerve block in patients undergoing stapled hemorrhoidectomy. This surgery is painful and use of regional analgesia technique as a part of multimodal analgesia regime is helpful for early rehabilitation of patient.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Investigator Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •â€¢ Patients undergoing stapled hemorrhoidectomy under GA • American society of anesthesiology (ASA) grade 1 and 2 patients.

Exclusion Criteria

  • •Patient refusal
  • •ASA 3 and above
  • •Patients with features of local infection at the site of block
  • •Patients with history of bleeding disorder or on anticoagulant therapy
  • •Patients with known allergy to local anesthetic drugs
  • •Patients with mental illness
  • •Patients with neuromuscular disorders.

Outcomes

Primary Outcomes

Time of requirement of first rescue opioid analgesic.

Time Frame: 0 , 4 , 8 ,12 and 24 hours

Secondary Outcomes

  • 1. To compare overall requirements for Opioids in 24 hours.(2. Pain score.)

Investigators

Sponsor
Not provided
Responsible Party
Principal Investigator
Principal Investigator

Dr Divesh Arora

Asian Hospital Faridabad

Study Sites (1)

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