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Arthroscopic Shoulder Surgery clinical trials

View clinical trials related to Arthroscopic Shoulder Surgery.

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NCT ID: NCT03212443 Completed - Clinical trials for Arthroscopic Shoulder Surgery

Combined Suprascapular and Axillary Nerve Blocks for Arthroscopic Shoulder Surgery

Start date: August 10, 2017
Phase: N/A
Study type: Interventional

Arthroscopic shoulder surgery is associated with severe pain postoperatively. Regional nerve block adding to general anesthesia might improve the quality of postoperative analgesia. The aim of the study is to compare the subacromial local anesthetic infiltration and the suprascapular-axillary nerve blocks combination for intraoperative sevoflurane consumption, postoperative analgesia and analgesic consumption.

NCT ID: NCT02867904 Terminated - Clinical trials for Arthroscopic Shoulder Surgery

Intra-Operative Corticosteroid Injection During Arthroscopic Shoulder Surgery

Start date: March 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the efficacy of intra-operative subacromial corticosteroid injections in patients undergoing arthroscopic shoulder surgery on quality of life scores and activity level when compared to a control group.

NCT ID: NCT01351363 Completed - Pain Threshold Clinical Trials

Prediction Of Post Operative Pain Following Arthroscopic Shoulder Surgery

Start date: March 2009
Phase: N/A
Study type: Interventional

Following arthroscopic shoulder surgery a small but significant number of people suffer severe postoperative pain. This study aims to predict which patients are at risk of developing severe post operative pain so that they may be targeted with a more aggressive post operative pain regimen.

NCT ID: NCT00731146 Recruiting - Clinical trials for Arthroscopic Shoulder Surgery

Effects of Technique on the Local Anesthetic Dose Required for Interscalene Brachial Plexus Block

Start date: August 2008
Phase: N/A
Study type: Interventional

Interscalene brachial plexus block (ISBPB) is a common nerve block given to patients who are undergoing shoulder surgery. This block has a low, but still significant, rate of complications. Reducing the volume of local anesthetic given during the block may allow some of these complications to be avoided. Participants will be randomly assigned to a group to undergo ISBPB under ultrasound or nerve stimulator guidance. Each group will initially receive 10mL of local anesthetic. The volume used for each subsequent patient depends upon the success or failure of the previous patient's block - a failure will cause the volume given to increase by 2.5mL, while a success will cause the volume to decrease by the same amount. We hypothesize that the minimum effective anesthetic volume in 50% of patients will be significantly lower in the ultrasound guided group than in the nerve stimulator group. We further hypothesize that this lower volume will lead to a decreased rate of complications.