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Fascia iliaca vs epidural block in patients undergoing total knee replacement surgery

“USG fascia iliaca block as an alternative to epidural block in patients undergoing TOTAL KNEE ARTHROPLASTY ?

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/08/027405
Enrollment
110
Registered
2020-08-26
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M170- Bilateral primary osteoarthritis of knee

Interventions

Intervention1: USG guided Fascia iliaca block-group 1: As a protocol in our institute every patient undergoing knee arthroplasty is given subarachnoid block unless contraindicated. The patient will

Sponsors

PGIMER CHANDIGARH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Study population will be randomized into two groups through computer generated random numbers and coded sealed envelope method. Envelope will be opened by a technical staff blind to the study. Group 1 USG guided fascia iliaca block Group 2 Epidural block As a protocol in our institute every patient undergoing knee arthroplasty is given subarachnoid block unless contraindicated. In our study either usg guided fascia iliaca block or epidural block will be given based on the randomization for postoperative analgesia. The patient will be shifted to the operating room and all standard ASA monitors will be attached and baseline vitals like blood pressure, heart rate, oxygen saturation will be noted. Under all aseptic precautions, local injection of lignocaine 2% w/v shall be infiltrated into the skin at the point of needle insertion. Group 1 patients will receive SAB followed by usg guided fascia iliaca block with 20 ml ,0.25% bupivacaine + 1mcg /kg of dexmedetomidine , a catheter will be put for postoperative drug infusion, while group 2 patients will be receiving lumbar epidural L2-L3 level and SAB.

Exclusion criteria

Exclusion criteria: 1) Age more than 80 years 2) severe COPD 3) severe life-threatening heart disease

Design outcomes

Primary

MeasureTime frame
Aim of this randomized prospective study is to compare pain scores between USG fascia iliaca block and epidural blockTimepoint: 1st hour,6th hour,12th hour,24hour

Secondary

MeasureTime frame
Total opioid consumption, motor power/weakness, time for ambulation, hypotension, nausea vomiting, and , any complicationon arising from fascia iliaca and epidural blockTimepoint: 1st hour,6th hour,12th hour,24th hour

Countries

India

Contacts

Public ContactSANJAY KUMAR

PGIMER CHANDIGARH

sanjayjaswal247@gmail.com9779170944

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026