To compare which group gives better pain relief in patients undergoing hip surgeries

Not yet recruiting

• Conditions: Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified,

• Registration Number: CTRI/2023/06/053501
• Lead Sponsor: indira ghandhi medical college and research institute

Brief Summary

The approval of the Institutional Research &Ethics Committee  will be  obtained  and the patients will  be  randomly allocated (computer-generated random numbers) to 2groups   Group I (PENG +PND) and   Group 2 (PENG +IVD) .

 Written  informed consent will be obtained from all patient participating in study.Inclusion criteria includes all American Society of Anesthesiologists physical status I and II , age greater than 18 years, weight greater than 50 kg,  scheduled for hip fracture surgeries (Intertrochanteric fracture ,Subcapital fracture,Hip hemiarthroplasty ,Total hip arthroplasty )will be  involved in the study. Postoperatively patients will be shifted to PACU ,where the Numeric rating score (NRS) will be recorded at 30 minutes at first , followed by 1st  , 4th  , 6th , 8th , 12th ,18th and 24 hr.If the Patient complains of pain  and if the   NRS >6 at any hour rescue analgesic of 1 gm  of intravenous paracetamol will be given.Injection fentanyl 1 mcg/kg iv will be given to patients who do not respond to in paracetamol 1 gm iv .Salvage analgesic needs and times will be noted in detail, and the use of rescue analgesics, as well as NRS scores at designated hours, will be kept in a statistical evaluation.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2023-05-25
• Study Start: 2024-10-05

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 48

Inclusion Criteria

• Patient willing to take part in the study.
• Age greater than 18 years including both the sex.
• ASA 1 and ASA 2 patients.
• Weight more than 50 kg.

Exclusion Criteria

• Patient refusal 2.
• Infection at the site of block 3.
• Contraindication to regional anaesthesia such as bleeding diathesis ,patients on anticoagulants 4.
• Known allergy to local anaesthetic​​​​​​ 5.
• Inability to provide the consent 6.
• Psychiatric patient.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Request for first postoperative analgesia	Time from which the block has performed to the time when the Numeric Rating Scale score is above 6 in minutes

Secondary Outcome Measures

Name	Time	Method
Ease positioning for spinal anaesthesia	1 hour

Trial Locations

Locations (1)

INDIRA GHANDHI MEDICAL COLLEGE AND RESEARCH INSTITUTE; 🇮🇳 Pondicherry, PONDICHERRY, India

INDIRA GHANDHI MEDICAL COLLEGE AND RESEARCH INSTITUTE

🇮🇳Pondicherry, PONDICHERRY, India

MALAINESAN E

Principal investigator

8531042984

malainesan231097@gmail.com