BiFeS vs. iPACK in Postoperative Knee Arthroplasty Analgesia
Recruiting
N/A
Interventional Study
Arthroplasty, Replacement, Knee
Pain, Postoperative
Anesthesia, Regional
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 80
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 88 (estimated)
- Sponsor
- Amasya University · Other
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
The Biceps Femoris Short Head (BiFeS) block is a new fascial plane block technique targeting the sensory innervation of the posterolateral capsule of the knee while preserving motor function. The aim of this study is to evaluate the postoperative analgesic efficacy of the BiFeS block combined with the adductor canal block (ACB) in patients undergoing total knee arthroplasty, compared to ACB + iPAC…
Trial Locations
Loading…
Loading trial locations…
Eligibility Criteria
Inclusion Criteria:
* Scheduled for unilateral total knee arthroplasty
* Classified as ASA physical status I-III
Exclusion Criteria:
* Scheduled for revision arthroplasty or bilateral surgery
* Allergy to local anesthetics or contraindication to regional blocks
* Neurological disorders, periphera…
Contacts