UnknownPhase 1

Comparative Study Between Ultrasound-Guided IPACK Block (Interspace Between the Popliteal Artery and the Posterior Capsule of the Knee) with Adductor Canal Block Versus Adductor Canal Block Alone for Postoperative Pain Management in Total Knee Arthroplasty

Egypt60 participantsStarted 2025-01-09

Plain-language summary

The investigators will compare the effectiveness of the interspace between the popliteal artery and posterior capsule of the knee (IPACK) block with adductor canal block versus adductor canal block alone for postoperative analgesia in total knee arthroplasty with consequently improved early ambulation and functional rehabilitation.

Who can participate

Age range20 Years – 60 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: \- Exclusion Criteria: * The patient refusal to give written consent. * Previously known allergy to one of the drugs being used in the study. * Physical status: ASA grades more than III * History or evidence of coagulopathy, use of anti-coagulant or anti-platelet therapy. * Patients with neuromuscular disorders * Injection site infection.

What they're measuring

The time interval between injection of the block and the first rescue analgesia dose given

Timeframe: 24 hours from block injection

Trial details

NCT IDNCT06783712

SponsorAin Shams University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-02-01

Contact for this trial

Hager Talal Mohamed, MBBCH

+201119050190 hager.talal5@gmail.com

View on ClinicalTrials.gov More The Time Interval Between Injection of the Block and the First Rescue Analgesia Dose Given. Postoperative Pain Assessment Using NRS Score for Pain trials