About this trial

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.

Eligibility criteria

Qualifiers

Adults aged 18 years or older

Clinical diagnosis of adhesive capsulitis of the shoulder

Persistent pain and functional limitation despite initial conservative treatment

Ability to understand study procedures

Disqualifiers

Known allergy or hypersensitivity to ropivacaine or methylprednisolone

Active infection (local or systemic)

Uncontrolled coagulopathy or ongoing therapeutic anticoagulation

Recent surgery of the affected shoulder

Trial design

Treatments tested in this trial

  • Shoulder Hydrodistention
  • suprascapular nerve block

Treatment groups

50 Participants
are divided into 2 treatment groups

Locations

1
Unidade Local de Saude São João, EPE4200-319, PortoPorto District, Portugal

Sponsors and collaborators

Universidade do Porto

Lead sponsor