NCT07135375 Postoperative Rotator Cuff Rehabilitation: Functional, Pain and Sleep Quality
| NCT ID | NCT07135375 |
| Status | Recruiting |
| Phase | — |
| Sponsor | LAURA CASTILLO VEJAR |
| Condition | Rotator Cuff Injuries |
| Study Type | INTERVENTIONAL |
| Enrollment | 50 participants |
| Start Date | 2025-08-26 |
| Primary Completion | 2025-11-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 50 participants in total. It began in 2025-08-26 with a primary completion date of 2025-11-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Rotator cuff injuries are the third leasing cause of pain and disability, accounting for 16% of all musculoskeletal injuries. Following surgical intervention, patients typically undergo a 4 to 6 week immobilization period before starting physical therapy. This rehabilitation phase can last between 4 to 6 months. Despite this, there is currently a lack of clear guidelines regarding specific physical therapy protocols or the expected post surgical recovery for patients who have undergone rotator cuff repair.
Eligibility Criteria
Inclusion Criteria: * People over 50 years of age * People have undergone arthroscopic rotator cuff of one or more tendons. * Patients must sign informed consent and undergo physical therapy center (up to week 12 postoperatively). Exclusion Criteria: * Patients who develop postoperative stiffness or adhesive capsulitis during the rehabilitation process. * Patients with symptoms of cervical radiculopathy or previously diagnosed sleep disorders. * Patients with neurological or cognitive disorders who have difficulty following instructions
Contact & Investigator
Laura LA Castillo-Vejar
PRINCIPAL INVESTIGATOR
TRIMEDKINE
Frequently Asked Questions
Who can join the NCT07135375 clinical trial?
This trial is open to participants of all sexes, aged 50 Years or older, studying Rotator Cuff Injuries. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07135375 currently recruiting?
Yes, NCT07135375 is actively recruiting participants. Contact the research team at lauracastillovejar@gmail.com for enrollment information.
Where is the NCT07135375 trial being conducted?
This trial is being conducted at Temuco, Chile, Temuco, Chile.
Who is sponsoring the NCT07135375 clinical trial?
NCT07135375 is sponsored by LAURA CASTILLO VEJAR. The principal investigator is Laura LA Castillo-Vejar at TRIMEDKINE. The trial plans to enroll 50 participants.