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Rotator Cuff Tear clinical trials

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NCT ID: NCT03149887 Completed - Rotator Cuff Tear Clinical Trials

Liposomal Bupivacaine After Arthroscopic Rotator Cuff Repair

Start date: December 5, 2017
Phase: Phase 4
Study type: Interventional

Liposomal bupivacaine, a long-acting form of bupivacaine, has been found to be effective for postoperative pain control after total knee, total hip and total shoulder arthroplasty. We are conducting a randomized, controlled trial to evaluate pain control after arthroscopic rotator cuff repair in ambulatory patients, comparing standard care in the control group, with standard care plus the addition of injection of liposomal bupivacaine in the experimental group.

NCT ID: NCT03073655 Completed - Rotator Cuff Tear Clinical Trials

The Effects of Kinesio Tape Application With Different Verbal Input Given to With Patients With Rotator Cuff Tear

Start date: January 2016
Phase: N/A
Study type: Interventional

The aim of the study to investigate the effectiveness KT application with different verbal inputs on pain, function and range of motion (ROM) on patient with rotator cuff tear.

NCT ID: NCT03054753 Completed - Rotator Cuff Tear Clinical Trials

Prospective Sensor Controlled Compliance Analysis of Shoulder Abduction Splint After Rotator Cuff Repair

SENSABDUKT
Start date: March 31, 2017
Phase: N/A
Study type: Interventional

The postoperative shoulder rehabilitation in an abduction brace after rotator cuff reconstruction of the shoulder is crucial for a successful healing of the reconstruction. In this study the investigators want to analyse the abduction brace-wearing time using a electronic sensor, which is implanted in the abduction brace. The participants will be informed about the sensor after completion of the abduction brace rehabilitation 6 weeks postoperatively.

NCT ID: NCT02976285 Completed - Rotator Cuff Tear Clinical Trials

Polyester Patch in Massive Rotator Cuff Repair Improves Healing

Start date: June 2012
Phase: N/A
Study type: Observational

The purpose of this study was to assess the impact and potential advantage of a novel synthetic patch augmentation in repair of massive rotator cuff (RC) tears, using clinical and radiological approaches. The investigators hypothesized that implanting this patch will improve individual shoulder function, while reducing re-tear rates compared to the current literature.

NCT ID: NCT02969135 Completed - Rotator Cuff Tear Clinical Trials

Progressive Active Exercise After Surgical Rotator Cuff Repair

Start date: February 26, 2017
Phase: N/A
Study type: Interventional

Shoulder disorders are extremely common, with a life-time prevalence in population of 30%. About 23% of the working population with shoulder problems are sick-listed. Specifically rotator cuff tears are considered some of the principal causes of chronic shoulder pain and disability, especially with advancing age. The National Patient Register in Denmark has registered 730 rotator cuff repairs in 2006 and 990 in 2012, which represents a 35% increase. A rotator cuff tear is defined as a rupture of the tendon (s) of the shoulder, and most frequently involves the supraspinatus and/or the infraspinatus tendon, resulting in loss of function due to pain and tissue weakness. Little is known about the effects of the postoperative training/rehabilitation, and this provides an unclear picture of the total treatment procedure of this condition. The Danish National Clinical Guidelines from 2013 recommend that these patients are offered rehabilitation and that the shoulder is immobilized post-surgery, but the evidence for postoperative training is moderate- low. The past few years, there have been conducted 5 systematic reviews looking at different rehabilitation parameters after rotator cuff surgery. They conclude that early Range-Of-Motion exercise accelerate healing, reduce stiffness, do not increase risk of re-rupture and that immobilization do not increase tendon healing or clinical outcome. They also conclude that there is a further need to evaluate approaches that foster early initiation of rehabilitation and gradual introduction of functional load in high-quality, adequately powered trials, also considering key outcomes such as return to work. Therefore, the aim of this study is to compare the effect of a progressive early passive and active movement protocol with a care as usual (limited early passive movement protocol) on tendon healing, physical function, pain, and quality of life, in patients operated due to traumatic full thickness rotator cuff tear in a Randomized Controlled Trial. Shortterm effects of physical function, pain, and quality of life will be studied as primary patient reported outcome, while secondary outcomes will be clinical and paraclinical outcomes in addition to the longterm effects of physical function, pain, and quality of life.

NCT ID: NCT02929433 Completed - Rotator Cuff Tear Clinical Trials

Cycloergometer and Rotator Cuff Tear

Start date: January 2013
Phase: N/A
Study type: Interventional

The cycloergometer is a mechanical device consisting of a bicycle frame fixed on a support base, designed to measure the amount of muscle work performed during exercise and the resistance to pedaling. The cycloergometer has been already employed in many fields of medicine. However, up to date, a little use of cycloergometer in the management of chronic joint diseases has been documented and scientific studies have not clarified if cycloergometer is effective in these diseases and, particularly, in Rotator Cuff Tear patients.

NCT ID: NCT02850211 Completed - Rotator Cuff Tear Clinical Trials

A Selective COX-2 Inhibitor Provides Pain Control But Hinders Healing Following Arthroscopic Rotator Cuff Repair

Start date: September 2011
Phase: Phase 4
Study type: Interventional

Selective cyclooxygenase (COX)-2 inhibitors are commonly used analgesics that provide similar analgesia but reduced adverse effects compared to other analgesics. However, few studies have been conducted on postoperative pain and tendon-to-bone healing. Here, the investigators investigated the effect of a selective COX-2 inhibitor on analgesia and tendon-to-bone healing following arthroscopic rotator cuff repair.

NCT ID: NCT02784600 Completed - Rotator Cuff Tear Clinical Trials

Rotation Medical Bioinductive Implant Database Registry

REBUILD
Start date: April 25, 2016
Phase:
Study type: Observational [Patient Registry]

The purpose of this clinical registry is to prospectively collect and compare preoperative and postoperative patient-reported data using validated shoulder-specific and health-related quality of life (QoL) instruments during real-world use of the Rotation Medical bioinductive implant to treat rotator cuff tears.

NCT ID: NCT02644564 Completed - Rotator Cuff Tear Clinical Trials

Early Clinical Examination and Ultrasonography Screening of Acute Soft Tissue Shoulder Injuries

Start date: October 5, 2015
Phase: N/A
Study type: Observational

The purpose of the study is to determine whether the introduction of early ultrasonography screening will change the diagnostic spectrum of soft tissue shoulder injuries in patients aged forty years or more. We also want to study whether certain physical tests will be able to predict or rule out full-thickness tears of the rotator cuff (shoulder tendons) in the acute phase. Another purpose is to explore the course of soft tissue shoulder injuries over a year, as well as to compare the results to studies on the prevalence of rotator cuff full-thickness tears.

NCT ID: NCT02643017 Completed - Rotator Cuff Tear Clinical Trials

Effect of Dexmedetomidine on Postoperative Cognitive Function in Patients Undergoing Shoulder Arthroscopy With Beach Chair Position Under Desflurane Anesthesia

Start date: December 11, 2015
Phase: N/A
Study type: Interventional

Investigate the effects of dexmedetomidine on postoperative cognitive function in patients undergoing shoulder arthroscopy with beach chair position under desflurane anesthesia.