Adhesive Capsulitis Shoulder

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Review clinical trials related to Adhesive Capsulitis Shoulder. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Suprascapular Nerve Block to Improve Tolerance and Outcomes of Shoulder Hydrodistension in Adhesive Capsulitis

Adhesive capsulitis ("frozen shoulder") causes significant pain and loss of shoulder mobility. Shoulder hydrodistension is an established treatment that can improve movement and reduce symptoms, but the procedure itself may be painful and difficult for some patients to tolerate. This randomized clinical trial will evaluate whether performing a suprascapular nerve block with local anesthetic immediately before hydrodistension can reduce pain during the procedure, improve patient comfort, and potentially enhance clinical outcomes. Participants will be randomly assigned to one of two groups: hydrodistension alone, or suprascapular nerve block followed by hydrodistension. Pain, shoulder mobility, functional ability, psychological measures, and quality of life will be assessed at baseline, 1 month, and 3 months after the procedure. The study aims to determine whether adding a suprascapular nerve block provides better tolerability and improved recovery for patients with adhesive capsulitis.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Universidade do PortoUpdated: Feb 2, 2026Locations: 1
Eligibility criteria

Adults aged 18 years or older [+4]

Known allergy or hypersensitivity to ropivacaine or methylprednisolone [+5]

Status: Not yet recruiting

Evaluating Upper Limb Movement Precision With AuReha in People With One-Sided Motor Impairment

The clinical investigation is designed as a controlled, two-arm, intra-patient, non-randomized interventional study aimed at assessing the capabilities of the AuReha system in detecting upper limb movement precision in patients with unilateral proprioceptive impairment. The comparison will be conducted within the same subject, between the healthy limb and the impaired limb, through the execution of proprioceptive exercises in an open kinetic chain. The biomechanical parameters collected will include movement precision, trunk stability, compensatory movements, and joint range of motion. In addition to the quantitative analysis, qualitative data will also be collected regarding usability, wearability, and user experience of the system through questionnaires administered to both patients and healthcare professionals. The study will be conducted at the Shoulder Team Outpatient Clinic in Forlì, enrolling approximately 52 patients.

Participants needed: 52
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: DigitalRehabUpdated: Oct 1, 2025Locations: 1
Eligibility criteria

patients with a healthy contralateral limb [+3]

Pregnant and/or breastfeeding women (verified through self-declaration) [+3]