Completed PHASE4 INTERVENTIONAL 2-arm NCT01818531

Adductor Canal Block for Medial Compartment Knee Arthroplasty

Evaluation of Ultrasound-Guided Adductor Canal Blockade for Postoperative Analgesia Following Robotic Medial Unicompartmental Knee Replacement

Sponsor: Wake Forest University Health Sciences

Conditions Medial Unicompartmental Knee Arthroplasty Postoperative Analgesia

Interventions Adductor canal block Lumbar plexus block

Updated 7 times since 2017 Last updated: Sep 12, 2018 Started: Apr 30, 2013 Primary completion: May 31, 2015 Completion: May 31, 2015

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This PHASE4 trial investigates Medial Unicompartmental Knee Arthroplasty and Postoperative Analgesia and is currently completed. Wake Forest University Health Sciences leads this study, which shows 7 recorded versions since 2013 — indicating limited longitudinal coverage. This study adds to the longitudinal dataset for psychiatric treatment development.

Status Flow

Change History

7 versions recorded

Sep 2024 — Present [monthly]

Completed PHASE4
Jul 2024 — Sep 2024 [monthly]

Completed PHASE4
Jan 2021 — Jul 2024 [monthly]

Completed PHASE4
Oct 2018 — Jan 2021 [monthly]

Completed PHASE4

Phase: NA → PHASE4
Jun 2018 — Oct 2018 [monthly]

Completed NA

▶ Show 2 earlier versions

Dec 2017 — Jun 2018 [monthly]

Completed NA
Jan 2017 — Dec 2017 [monthly]

Completed NA

First recorded

Apr 2013

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Wake Forest University Health Sciences

Data source: Wake Forest University Health Sciences

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Winston-Salem, United States