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Compare pain efficacy with and without iliopsoas plane block in patients undergoing total hip arthroplasty

Phase 4
Not yet recruiting
Conditions
Health Condition 1: M169- Osteoarthritis of hip, unspecifiedHealth Condition 2: M169- Osteoarthritis of hip, unspecifiedHealth Condition 3: M161- Unilateral primary osteoarthritisof hip
Registration Number
CTRI/2024/06/069175
Lead Sponsor
All India Institute of Medical Sciences, Patna
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients planned for total hip arthroplasty

ASA I, II, III patients

Age group 20- 70 years

Exclusion Criteria

Patient refusal

ASA IV

High risk patients who may require post operative ICU care

Infection over target site

Bleeding diathesis

Allergic to local anaesthetic

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the postoperative opioid consupmtion with and without iliopsoas plane 24hr post operativelyTimepoint: At 1hr, 6hr, 12hr, 24hr postoperatively
Secondary Outcome Measures
NameTimeMethod
Muscle power at 1hr 6hr 12hr 24hr postoperativelyTimepoint: At 1hr, 6hr, 12hr,24 hr postoperatively;NRS score at 1hr 6hr 12hr 24hr postoperativelyTimepoint: At 1hr, 6hr, 12hr, 24hr postoperatively;Patient satisfactionTimepoint: 24 hr postoperatively;Post operative time to 1st rescue analgesiaTimepoint: from the time of administration of block to the first need of resue analgesic administration;Postoperative nausea and vomitingTimepoint: 24 hr postoperatively
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