Trials / Completed
CompletedNCT03703206
The Analgesic Efficacy of Protocol for Primary Total Knee Arthroplasty (TKA)
The Analgesic Efficacy of Adding the IPACK Block to a Multimodal Analgesia Protocol for Primary Total Knee Arthroplasty
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 120 (actual)
- Sponsor
- University of Pennsylvania · Academic / Other
- Sex
- All
- Age
- 18 Years – 99 Years
- Healthy volunteers
- Not accepted
Summary
This is a perspective, randomized, blinded study with a parallel design and an allocation ratio of 1 to 1 for the treatment groups to assess the analgesic efficacy of adding the iPACK (injection between the popliteal artery and the capsule of the knee) in addition to the adductor canal block (ACB) for Total Knee Arthoplasty patients (TKA).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | ultrasound guided injection of local anesthetic between the popliteal artery and the capsule of the knee (iPACK) | nerve block for posterior knee pain after a TKA. |
Timeline
- Start date
- 2018-07-01
- Primary completion
- 2019-08-27
- Completion
- 2021-08-27
- First posted
- 2018-10-11
- Last updated
- 2024-05-30
- Results posted
- 2024-05-30
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03703206. Inclusion in this directory is not an endorsement.