Actively Recruiting

Phase 2
Phase 3
Age: 30Years - 60Years
All Genders
NCT07221682

Comparison of Supra vs Infra Inguinal Fascia Iliaca Blocks for Spinal Positioning and Analgesia in Lower Limb Surgery

Led by Sahiwal medical college sahiwal · Updated on 2026-01-29

60

Participants Needed

1

Research Sites

138 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Severe pain associated with thigh and knee fractures makes the positioning for regional anesthesia a challenge. Different modalities to make patient pain free for spinal positioning, post op analgesia and patient satisfaction including supra-inguinal fascia iliaca block (S-FIB) and infra-inguinal fascia iliaca blocks (I-FIB) have been studies. The aim of this study is to compare two blocks in patients undergoing thigh and knee surgeries. A randomized controlled trial study design will be used and 60 patients fulfilling the inclusion criteria will be included. The patients will be divided into 2 groups by simple random sampling. Group A (S-FIB) (n = 30, those who will receive 30 ml of 0.125% bupivacaine) and Group B (I-FIB) (n = 30, those who will receive 30 ml of 0.125% bupivacaine). Depending on the allotted group, patients will be given the block under the guidance of ultrasound in the preoperative area. After block patients will be assessed for ease of spinal positioning using EOSP Scale, postoperative duration of analgesia and patient satisfaction using Likert Scale and data will be recorded on prescribed proforma. All the findings will be noted in a specially designed proforma by the researcher. All the data collected will be entered and analyzed. Quantitative variables will be presented with mean ± SD. Independent sample t-test for duration of postoperative analgesia. Qualitative variables such as ease of spinal positioning and gender will be presented with Chi-Square. A p-value equal to or less than 0.05 will be considered significant.

CONDITIONS

Official Title

Comparison of Supra vs Infra Inguinal Fascia Iliaca Blocks for Spinal Positioning and Analgesia in Lower Limb Surgery

Who Can Participate

Age: 30Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Both genders (male and female)
  • Age between 30 and 60 years
  • Classified as ASA Class I, II, or III
Not Eligible

You will not qualify if you...

  • Patient refusal to participate
  • Presence of other distracting painful conditions
  • Contraindications to spinal anesthesia or peripheral nerve blocks
  • Blood clotting disorders
  • Significant cognitive impairment
  • No pain when sitting without support
  • History of multiple trauma involving other limbs
  • Allergy to drugs used in the study

AI-Screening

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Trial Site Locations

Total: 1 location

1

Sahiwal Medical College Sahwal

Sāhīwāl, Punjab Province, Pakistan, 57000

Actively Recruiting

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Research Team

D

Dr Humaira Shahzadi, MBBS

CONTACT

D

Dr Muhammad Shahid, FCPS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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