Factors influencing postoperative outcomes in shoulder contracture

JRCT ID: jRCT1031200095

Registered date:25/08/2020

Basic Information

• Recruitment status: Pending
• Health condition(s) or Problem(s) studied: Shoulder joint contracture
• Date of first enrollment: 25/08/2020
• Target sample size: 80
• Study type: Interventional

Intervention(s)

Intra-articular injection of triamcinolone immediately after surgery.
Wear a CPM device from the day after surgery until the 7th day after surgery.
One or both of the above.

Outcome(s)

• Primary Outcome: Shoulder range of motion
• Secondary Outcome: Pain, Strength, Shoulder function score

Key inclusion & exclusion criteria

• Age minimum: >= 20age old
• Age maximum: Not applicable
• Gender: Both

Include criteria

1) 20 years of age or older
2) Patients with shoulder pain
3) Patients with passive range of motion limitations (passive flexion and abduction less than 90 degrees or external rotation less than 10 degrees or internal rotation 5th lumbar vertebrae)
4) Patients undergoing arthroscopic capsular reliese
5) Patients with written consent to participate in this study

Exclude criteria

1) Patients with a history of previous surgery on the affected shoulder.
2) Patients with conditions such as rotator cuff tear, calcific tendonitis, or long head biceps tendon injury.
3) Patients who are contraindicated for the drug to be administered.
4) Patients with poorly controlled (HbA1C > 8.0) diabetes mellitus.
5) Patients with neurological or psychiatric disorders.
6) Other patients who are judged by a physician to be unsuitable for inclusion.

Related Information

• Primary Sponsor: Shitara Hitoshi