Completed NA INTERVENTIONAL 3-arm NCT01126593

Post-Op Rotator Cuff Pain Study With Subacromial Bupivacaine Infusion

Efficacy of Continuous Subacromial Bupivacaine Infusion for Postoperative Analgesia After Arthroscopic Rotator Cuff Repair.

Sponsor: Orlando Health, Inc.

Conditions Rotator Cuff Tear

Interventions 0.5% bupivacaine Normal Saline

Updated 9 times since 2017 Last updated: Nov 6, 2014 Started: Dec 31, 2008 Primary completion: Nov 30, 2009 Completion: Feb 28, 2010

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

This NA trial investigates Rotator Cuff Tear and is currently completed. Orlando Health, Inc. leads this study, which shows 9 recorded versions since 2008 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.

Status Flow

Change History

9 versions recorded

Sep 2024 — Present [monthly]

Completed NA
Jul 2024 — Sep 2024 [monthly]

Completed NA
Jan 2023 — Jul 2024 [monthly]

Completed NA
Dec 2022 — Jan 2023 [monthly]

Completed NA
Dec 2021 — Dec 2022 [monthly]

Completed NA

▶ Show 4 earlier versions

Jan 2021 — Dec 2021 [monthly]

Completed NA
Jun 2018 — Jan 2021 [monthly]

Completed NA
Feb 2017 — Jun 2018 [monthly]

Completed NA
Jan 2017 — Feb 2017 [monthly]

Completed NA

First recorded

Dec 2008

Trial started

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

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Orlando Health, Inc.

Data source: Orlando Health, Inc.

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

Study Locations

• Orlando, United States