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Arthroscopy clinical trials

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NCT ID: NCT06208774 Recruiting - Anesthesia Clinical Trials

Pericapsular Nerve Group Block vs Interscalene Block for Shoulder Arthroscopy

Start date: December 20, 2023
Phase: N/A
Study type: Interventional

This study aims to compare PENG block and LV-ISBP block in the incidence of phrenic nerve block, duration of postoperative analgesia, time to first analgesic request (VAS > 30 mm), pain scores, and side effects.

NCT ID: NCT06014203 Recruiting - Edema Clinical Trials

Examination of Edema After Arthroscopic Shoulder Surgery

Start date: September 1, 2023
Phase:
Study type: Observational

The investigators's aim is to examine trunk and upper extremity edema after arthroscopic rotator cuff repair and/or labrum repair surgeries. During surgery, the shoulder joint capsule is cut and the joint is entered arthroscopically. During this procedure, approximately 3-6 liters of saline fluid is injected into the joint, depending on the duration of the surgery. The given fluid accumulates out of the joint in relation to the duration of the surgery and the amount of fluid given. In this study, the investigators aim is to examine how much the extra-articular fluid collects under the skin of the upper extremity and trunk, and the change in the amount of fluid 24 hours after surgery. Examination of the amount of subcutaneous fluid may help to better understand the postoperative complications such as edema, carpal tunnel syndrome, compartment syndrome, myolysis, and dyspnea. How much edema the joint and surrounding structures are exposed to and its relationship with the duration of surgery can help to clinicians determine the safe discharge time.

NCT ID: NCT05995795 Not yet recruiting - Arthroscopy Clinical Trials

Arthroscopic Release Of Shoulder Internal Rotation Contracture In Brachial Plexus Palsy

Start date: September 1, 2023
Phase:
Study type: Observational

The purpose of this study is to evaluate the efficacy periarticular capsuloligamentous arthroscopic release of shoulder internal rotation contracture in brachial plexus palsy without any further intervention as tendon transfer.

NCT ID: NCT05658289 Recruiting - Bone Loss Clinical Trials

Latarjet vs Anatomic Glenoid Reconstruction

Start date: April 24, 2023
Phase: N/A
Study type: Interventional

Anterior shoulder dislocations occur when the humeral head translates anterior to the glenoid cause pain, stiffness, and glenoid bone loss. If left untreated, the risk of recurrence can be up to or greater than 90%. The only surgically modifiable factor to reduce the risk of recurrence is the glenoid bone loss (GBL), where surgeons have the ability to recreate the shape of the glenoid and reduce the risk of recurrent shoulder dislocations. Established boney procedures for shoulder instability include the Latarjet and free bone block procedures, such as the Anatomic Glenoid Reconstruction (AGR). The Latarjet is well known for its lower rate of recurrent instability, but raises concerns due to under-appreciated complications rates. The AGR is a newer surgical approach that has garnered attention for its low rate of recurrent instability and complication profile. Both treatments can reduce pain, increase function following surgery and reduce the risk of recurrent instability. However, these two established approaches have yet to be directly compared and studied on a larger scale. The purpose of this randomized control trial is to compare clinical and radiographic outcomes pre- and post-operatively between the Latarjet to the AGR.

NCT ID: NCT05646654 Recruiting - Clinical trials for Erector Spinae Plane Block

Interscalene Block Versus Erector Spinae Plane Block for Shoulder Arthroscopy Anesthesia

Start date: December 15, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effectiveness of ESPB versus ISB in anesthesia for shoulder arthroscopy

NCT ID: NCT05457452 Not yet recruiting - Clinical trials for Anterior Cruciate Ligament Injuries

Functional Outcomes Comparison in Patients Using Knee Brace Post ACL Reconstruction With Autograft Bone Quadricep Tendon

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

This study is a study looking for the relationship between variables with a prospective cohort design to determine functional outcomes subjectively and objectively in patients with and without braces after ACL reconstruction with bone quadriceps tendon per arthroscopy.

NCT ID: NCT05269095 Not yet recruiting - Arthroscopy Clinical Trials

Adductor Canal Block Combined With IPACK vs Genicular Nerves Block in Knee Arthroscopy

Start date: March 21, 2022
Phase: N/A
Study type: Interventional

This prospective randomized controlled study is designed to investigate the postoperative analgesic effect of adductor canal block (ACB) combined with infiltration of the interspace between the popliteal artery and the capsule of posterior knee (IPACK) block compared to genicular nerves block in patients undergoing knee arthroscopy.

NCT ID: NCT05222334 Not yet recruiting - Analgesia Clinical Trials

Ultrasound-Guided Extrafascial Versus Intrafascial Interscalene Brachial Plexus Block in Shoulder Arthroscopy

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

The aim of the study is to compare the diaphragmatic excursion and postoperative analgesia in the extrafascial versus intrafascial Interscalene brachial plexus block in patients undergoing shoulder arthroscopy.

NCT ID: NCT05165836 Completed - Analgesia Clinical Trials

Dexmedetomidine as Adjuvant in Erector Spinae Plane Block After Shoulder Arthroscopy

Start date: December 25, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of adding dexmedetomidine as an adjuvant to bupivacaine in ultrasound (US) guided erector spinae plane block (ESPB) for managing acute postoperative pain in patients undergoing shoulder arthroscopy.

NCT ID: NCT04855877 Recruiting - Clinical trials for Anterior Cruciate Ligament Rupture

Oral Administration of Tranexamic Acid in Anterior Cruciate Ligament Surgery Reduce Postoperative Haemarthrosis

Start date: July 6, 2021
Phase: Phase 4
Study type: Interventional

To find superiority relationship between oral and intravenous administration of tranexamic acid on peroperative and postoperative blood loss, haemarthrosis prevalence and improvement functional prognosis in anterior cruciate ligament arthroscopy.