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Suprascapular Nerve Block in Patients Rehabilitated After Arthroscopic Rotator Cuff Repair

The Effect of Suprascapular Nerve Block in Patients Rehabilitated After Arthroscopic Rotator Cuff Repair: Randomized Controlled Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06272786
Enrollment
36
Registered
2024-02-22
Start date
2024-07-28
Completion date
2025-03-01
Last updated
2024-08-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nerve Block, Pain, Rotator Cuff Tears

Keywords

Rotator Cuff Tears, pain, nerve block, rehabilitation

Brief summary

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.

Detailed description

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 There are many studies in the literature on suprascapular, axillary, and interscalene nerve blocks in early pain management after shoulder arthroplasty. All of these focus on pain in the perioperative or early postoperative period. There is a study on USG-guided suprascapular nerve block. In this study, unlike the studies in the literature, it was aimed to show the effectiveness of USG-guided suprascapular nerve block in the subacute rehabilitation process of patients.

Interventions

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.

PROCEDURESuprascapular nerve block

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.

Sponsors

Kirsehir Ahi Evran Universitesi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Investigator and outcome assessor will be different persons.

Intervention model description

Randomised controlled

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

-Having undergone arthroscopic rotator cuff repair surgery within the last week

Exclusion criteria

* History of previous surgery on the same shoulder * History of systemic inflammatory rheumatological disease * Neurological diseases with muscle weakness in the upper extremity (MS, ALS, Muscular -Dystrophy) * History of malignancy, pregnancy, breastfeeding * Use of steroids or immunosuppressive drugs * History of allergic reactions to local analgesics * Fibromyalgia syndrome * Chronic painful conditions that require opioid use * Presence of known psychiatric disease * Cognitive impairment (Mini Mental Test Score \<23)

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog Scale (VAS)BaselineIn the study, pain intensity was evaluated with the Visual Analogue Scale (VAS). Numbers from 0 to 10 on VAS; Patients will be asked to score their pain levels at rest, activity and at night, with 0 being defined as no pain and 10 being unbearable pain. Increased scores indicate higher pain intensity.
Shoulder joint range of motion (ROM)BaselineJoint range of motion will be measured and recorded passively in all directions using a goniometer according to the neutral zero method.

Secondary

MeasureTime frameDescription
Shoulder Pain and Disability Index (SPADİ)BaselineSPADI is a scale consisting of a total of 13 questions with 2 subscales: pain and disability. The score of the total and all sub-parameters is evaluated on a scale of 0-100. A high score indicates increased pain and impaired shoulder function.
Modified Constant-Murley Scoring6th weekModified Constant-Murley Scoring includes a total of four parameters: pain, activities of daily living (ADL), active ROM and strength. The total score is evaluated on a scale of 0-100 points by summing all subparametricS. A low score reflects increased pain and impaired shoulder functions, both in terms of subparametrics and the total score.

Countries

Turkey (Türkiye)

Contacts

Primary ContactBasak Cigdem Karacay, Asst Prof
basakcigdem@hotmail.com+9 0386 280 51 00.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026