Suprascapular Nerve Block in Patients Rehabilitated After Arthroscopic Rotator Cuff Repair

Sponsor
Kirsehir Ahi Evran Universitesi
Study ID
NCT06272786
Status
Recruiting
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Conditions

  • Nerve Block
  • Pain
  • Rotator Cuff Tears

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • conventional physiotherapy program. — PROCEDURE
    It will be applied to a rehabilitation program including joint range of motion exercises and physical therapy modalities by a physiotherapist at the Physical Therapy Hospital.
  • Suprascapular nerve block — PROCEDURE
    Bupivacaine hydrochloride will be used in this injection. 5 ml of bupivacaine hydrochloride 5% and 5 ml of saline will be drawn into a 10 ml syringe and ejection will be performed from the superior of the suprascapular noch under USG guidance.

Study Details

Suprascapular nerve block is an injection method that has been shown to be effective in shoulder rehabilitation in diseases such as adhesive capsulitis and stroke .. Applying the block under USG guidance instead of blinding increases the effectiveness and reduces complications.

Key Dates

First listed
Feb 22, 2024
Start date
Jul 28, 2024
Status verified
Aug 2024
Primary completion
Feb 1, 2025
Completion
Mar 1, 2025

Study Design

Enrollment
36 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Experimental Group
    In addition to the conventional physiotherapy program, patients in the intervention group will receive a suprascapular nerve block with musculoskeletal USG guidance available in our clinic at the beginning of rehabilitation. Bupivacaine hydrochloride will be used in this injection. 5 ml of bupivacaine hydrochloride 5% and 5 ml of saline will be drawn into a 10 ml syringe and ejection will be performed from the superior of the suprascapular noch under USG guidance.
  • Active Comparator: Control Group
    Patients in the control group will only receive a conventional physiotherapy program.

Primary Outcome Measure

Visual Analog Scale (VAS) [ Time Frame: Baseline ]

Central Contacts

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