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Shoulder Arthroscopy clinical trials

View clinical trials related to Shoulder Arthroscopy.

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NCT ID: NCT06235879 Recruiting - Clinical trials for Shoulder Arthroscopy

Comparison Between Pericapsular Nerve Group (PENG) Block and Interscalene Brachial Plexus Block for Postoperative Analgesia Following Shoulder Arthroscopy

Start date: February 1, 2024
Phase: N/A
Study type: Interventional

The study aimed to compare ultrasound guided pericapsular nerve group (PENG) block versus interscalene brachial plexus block for postoperative analgesia following shoulder arthroscopy.

NCT ID: NCT05788367 Recruiting - Clinical trials for Shoulder Arthroscopy

Pericapsular Nerve Block Versus Interscalene Nerve Block for Acute Pain Management in Shoulder Arthroscopy

Start date: July 15, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to compare PENG and ISB after shoulder arthroscopy for postoperative pain management after shoulder arthroscopy.

NCT ID: NCT05727345 Recruiting - Clinical trials for Shoulder Arthroscopy

Shoulder Anterior Capsular Block and Interscalene Brachial Plexus Block for Shoulder Arthroscopy

Start date: June 30, 2022
Phase: N/A
Study type: Interventional

The aim of our study is to reveal a comparison between interscalene brachial plexus block and shoulder anterior capsular block with respect to their efficacy on pain relief during perioperative anesthetic management. As intraoperative hemodynamic stability is an important factor for surgeons to achieve better outcomes because of its effect on the quality of arthroscopic visualization for shoulder arthroplasty, the investigators will also observe the effects of this matter. 50 patients scheduled for elective surgery will be randomized by closed envelope method into two groups (n=20) receiving either interscalene brachial plexus block or shoulder anterior capsular block preoperatively. Each group receives standardized general anesthesia and perioperative pain management protocol. Data to be recorded are numeric rating scales, intraoperative and postoperative analgesic use, intraoperative hemodynamic parameters, and arthroscopic visualization score. Moreover, block performance time, motor block, and side effects or complications will be noted.

NCT ID: NCT05453266 Completed - Rotator Cuff Tears Clinical Trials

Arthroscopic Rotator Cuff Repair Performed With Intraarticular Tranexamic Acid Could it Provide Improved Visual Clarity and Less Post-operative Pain? A Prospective, Double Blind, Randomized Study of 64 Patients.

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Shoulder arthroscopy is widely used for treatment of different shoulder pathologies. Visual clarity is essential for successful and safe surgery. The aim of present study is to determine whether intraarticular use of tranexamic acid (TXA) in surgery fluid can improve visual clarity and early postoperative pain.

NCT ID: NCT05244525 Completed - Clinical trials for Shoulder Arthroscopy

Subacromial Injection of Epinephrine Improves Visualization in Shoulder Arthroscopy

Start date: March 14, 2022
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate surgeon-rated visual clarity and the need for increased irrigation pump pressure during arthroscopic shoulder surgery and to evaluate mean arterial pressure, operative time, and any adverse events that occur during arthroscopic shoulder surgery.

NCT ID: NCT04610164 Enrolling by invitation - Postoperative Pain Clinical Trials

The Effect of Tranexamic Acid (TXA) on Visualization During Shoulder Arthroscopy

Start date: June 19, 2019
Phase: Phase 3
Study type: Interventional

Tranexamic acid has seen an increase in use over the past decade in hip and knee arthroplasty as well as spine surgery with more recent use seen in total shoulder arthroplasty (TSA). The mechanism of action of TXA is as a lysine analogue that competitively inhibits the conversion of plasminogen to plasmin thus resulting in its antifibrinolytic activity. Investigators have showed that compared with placebo TXA had a statistically significant effect on blood and postoperative hemoglobin levels in TSA. To date there are no studies investigating the effect of TXA in arthroscopy of any kind or studies examining the ability of TXA to aid in surgeon visualization in arthroscopic procedures. The investigators of this study will use change in pump pressure as a surrogate objective measure for surgeon visualization. The hypothesis is that participants who receive TXA will have a lower change in pump pressure compared to participants who do not receive TXA.

NCT ID: NCT04566250 Completed - Knee Arthroscopy Clinical Trials

Non-Opioid Prescriptions After Arthroscopic Surgery in Canada (NO PAin)

NO PAin
Start date: February 24, 2021
Phase: N/A
Study type: Interventional

This is a randomized controlled trial of 200 patients between the ages of 18 and 65 years undergoing outpatient knee or shoulder arthroscopy. Patients will be evaluated clinically at 2 and 6 weeks post-operatively. Patients will be recruited from experienced arthroscopic surgeons at 3 hospital sites in Hamilton, Ontario. All research will be conducted according to international standards of Good Clinical Practice and institutional research policies and procedures.

NCT ID: NCT04483323 Completed - Clinical trials for Postoperative Analgesia

Erector Spinae Plane Block Versus Intraarticular Injection for Postoperative Analgesia in Shoulder Arthroscopy

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

To improve the outcome after surgery, effective pain control is needed. The aim of the current study was to compare the efficacy of ultrasound guided erector spinae plane block versus the intra articular injection of local anesthetic for post-operative analgesia in patients undergoing shoulder arthroscopy.

NCT ID: NCT03216590 Not yet recruiting - Clinical trials for Shoulder Arthroscopy

The Effect of Draping on Swelling in Shoulder Arthroscopy

Start date: July 20, 2017
Phase: N/A
Study type: Interventional

Strategies to minimize soft tissue swelling during shoulder arthroscopy are constantly sought after. The investigators propose an unfamiliar method which may reduce tissue swelling during shoulder arthroscopy.

NCT ID: NCT02688530 Completed - Pain Clinical Trials

Intravenous Dexamethasone on Supraclavicular Brachial Plexus Block for Shoulder Arthroscopy

SCB & IV Dex
Start date: May 2016
Phase: Phase 4
Study type: Interventional

Previous studies have confirmed that IV dexamethasone prolongs brachial plexus blocks. However, these studies only used fixed doses of IV dexamethasone at relatively high doses, which could potentially lead to increased glucose levels, delayed wound healing, and unintended side effects. There remains a paucity of research on the effective dose range of IV dexamethasone for the prolongation of supraclavicular blocks. The optimal dosage of IV dexamethasone for prolongation of analgesia vs. motor block prolongation from supraclavicular blocks in shoulder surgery has yet to be delineated.