Comparision of Hydrodilatation Results at Different Volumes in Adhesive Capsulitis by Phases.

Last updated: April 18, 2025
Sponsor: Javier Muñoz Paz
Overall Status: Active - Recruiting

Phase

N/A

Condition

Bursitis

Treatment

Hydrodilatation (20 ml)

Hydrodilatation (40 ml)

Clinical Study ID

NCT06939530
HYCAFVOL
  • Ages 30-70
  • All Genders

Study Summary

Adhesive capsulitis (AC) causes a global limitation of active and passive range of motion (ROM) in the shoulder, with or without pain, and no other radiographic findings. The natural process is self-limiting, evolving in three or four phases. It is common in women around 50 years of age. Diagnosis is based on clinical symptoms, with imaging tests being nonspecific. Treatment options include physical therapy (PT), intra-articular corticosteroid injections, suprascapular nerve block (SSNB), and hydrodilatation (HD). The latter is useful for expanding and reducing inflammation of the joint capsule through insufflation with saline solution, anesthetics, and corticosteroids.

Objectives: To determine whether patients with AC, stratified by phase, who receive high-volume HD therapy achieve better outcomes in the Shoulder Pain and Disability Index (SPADI), Analgesic Analogue Scale (VAS), and ROM at the first, third, and sixth months of therapy compared to patients who receive low-volume HD. To determine whether there are differences in FST times and to determine mean axilar recess (AR) values.

Methods: A randomized, triple-blind, parallel-block clinical trial will be conducted in 64 patients with AC in phases 1 and 2, aged 30 to 70 years, with limited active and passive ROM in two planes, and shoulder pain lasting more than 3 months. HD will be administered with volumes of 20 ml or 40 ml, followed by a physical therapy program. Outcomes will be reviewed at the first, third, and sixth months of HD. Variables collected will include SPADI, VAS, ROM, Lattinen assessment, AR size, and time to completion of PT

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Ages between 30 and 70 years.

  • Limited ROM, both active and passive, in two planes.

  • Shoulder pain lasting more than 3 months.

Exclusion

Exclusion Criteria:

  • Lidocaine + trial with improved ROM.

  • Conditions that preclude treatment (active cancer, tissue infection, oralanticoagulant use, cardiac arrhythmias, etc.)

  • Previously receiving HD treatment in less than 1 year.

  • Stage 0 or 3 AC.

  • Non-adherence to the PT program, with attendance failures exceeding 20%.

  • Presence of conditions that can cause similar symptoms, such as acromioclavicularosteoarthritis, labral injury, massive rotator cuff tear, or rheumatic diseases.

  • Intra-articular corticosteroid injection in less than 2 months.

  • Technique failure.

Study Design

Total Participants: 64
Treatment Group(s): 2
Primary Treatment: Hydrodilatation (20 ml)
Phase:
Study Start date:
February 02, 2025
Estimated Completion Date:
January 31, 2026

Connect with a study center

  • Hospital Universitario Reina Sofia

    Córdoba, 14004
    Spain

    Active - Recruiting

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