Pain Levels and Opioid Usage in Three Nerve Block Cohorts in Primary TKA

Withdrawn before enrolling · Not applicable

Conditions studied: Knee Arthropathy

In brief

The primary objective of this study is to compare effect of combined block of ACB (adductor canal block) with IPACK (Interspace between the Popliteal Artery and the Capsule of the posterior Knee) block and/or Intra-articular block in immediate postoperative and early postop rehabilitation and pain management in patients undergoing primary TKA. The secondary objective is to review both in-hospital and post-discharge pain levels and narcotic usage of primary TKAs, with a minimum 6-week postoperative follow-up.

Key facts

Study ID

NCT04292392

Run by

University of Louisville

People needed

0

Starts

2020-04-06

Expected to finish

2020-09-30

Last updated by the study team

2020-11-04

Who can join

Age: 22 and older, up to 89. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient is indicated for a primary, unilateral TKA secondary to osteoarthritis.
• Patient age is 22-89 at time of TKA surgery.
• Patient agrees to participate as a study subject and signs the Informed Consent and Research Authorization document.
• Patient is able to read and speak English.

You may not qualify if…

• Patient is under the age of 22 or over the age of 89.
• Patient's primary diagnosis is not osteoarthritis (e.g. post-traumatic arthritis).
• Patient is scheduled to undergo a bilateral TKA surgery.
• Patient is unable to read and speak English.

Where it is running

• Jewish Hospital — Louisville, Kentucky, United States

Full record on ClinicalTrials.gov

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