Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Both genders (male and female)
- Age between 30 and 60 years
- Classified as ASA Class I, II, or III
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
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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