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Clinical Trials/CTRI/2024/12/078279
CTRI/2024/12/078279
Not yet recruiting
Phase 4

Ultrasound-guided erector Spinae plane block versus ilioinguinal/iliohypogastric block for postoperative analgesia in patients undergoing inguinal surgeries : A randomised clinical trial

Dr Neha Chajgotra1 site in 1 country100 target enrollmentStarted: January 1, 2025Last updated:

Overview

Phase
Phase 4
Status
Not yet recruiting
Sponsor
Dr Neha Chajgotra
Enrollment
100
Locations
1
Primary Endpoint
1) Severity of pain using Numerical Rating Scale (NRS)

Overview

Brief Summary

This study is a randomised, parallel group, clinical trial comparing the effectiveness of two blocks i.e ultrasound guided Erector Spinae plane block versus ilioinguinal/ iliohypogastric block for postoperative analgesia in patients undergoing inguinal surgeries, as measured by duration of analgesia and pain score in 24 hours following surgery. The primary outcome of the study is to record the severity of pain using Numerical rating scale and time to request of first analgesia i.e the time elapsed between the end of surgery to 1st dose of analgesia. The secondary outcome is to see the total no. of analgesic doses of opioids and NSAIDs in 24 hours following surgery and to see any side effects like nausea, vomiting and shivering occurring after the procedure.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

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

Inclusion Criteria

  • patients between age group of 18 years to 60years who are undergoing inguinal hernia repair in elective OT 2) ASA class 1 & 2 3) patients who are willing to participate and provide a willing written informed consent.

Exclusion Criteria

  • patients with any chronic medical illness 2) history of any bleeding disorders 3) patients allergic to any of these drugs.

Outcomes

Primary Outcomes

1) Severity of pain using Numerical Rating Scale (NRS)

Time Frame: Severity of pain using Numerical Rating Scale (NRS) at 1,2,6,12 and 24 hours after surgery

2) Time to 1st request of analgesia

Time Frame: Severity of pain using Numerical Rating Scale (NRS) at 1,2,6,12 and 24 hours after surgery

Secondary Outcomes

  • 1) Total number of analgesic doses of opioids and NSAIDS in 24 hours following surgery(2) side effects like nausea, vomiting and shivering)

Investigators

Sponsor
Dr Neha Chajgotra
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr Neha Chajgotra

Government Medical College Kathua

Study Sites (1)

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