Suprascapular Nerve Block in the Management of Patients Diagnosed With Adhesive Capsulitis

NCT ID: NCT07097571

Last Updated: 2025-07-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-26

Study Completion Date

2026-08-26

Brief Summary

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This study aims to compare the efficacy of different suprascapular nerve block techniques in patients diagnosed with adhesive capsulitis.

Adhesive capsulitis, commonly known as frozen shoulder, is a condition characterized by pain and restricted range of motion in the shoulder joint, significantly affecting quality of life. The suprascapular nerve provides sensory innervation to the shoulder joint; therefore, nerve blockade is frequently used to alleviate pain. However, there are limited studies evaluating the difference in efficacy between proximal and distal suprascapular nerve blocks.

In this research, two different blockade techniques-at the suprascapular notch and the spinoglenoid notch-will be compared in patients diagnosed with adhesive capsulitis at Istanbul University-Cerrahpaşa between 2024 and 2026. The hypothesis of the study is that the block performed at the spinoglenoid notch provides pain relief comparable to the suprascapular notch block while resulting in less motor blockade.

Patients participating in the study will be randomly assigned to two groups. Both groups will receive an intra-articular corticosteroid injection into the shoulder joint, along with cold application, Codman exercises, and standard medical therapy. Pre- and post-treatment evaluations will include pain severity (NRS), shoulder function (Modified Constant Score), muscle strength, and range of motion.

The results will reveal which technique provides better improvement in shoulder external rotator and abductor muscle strength, shoulder function, and pain relief, thereby offering valuable insights to guide treatment approaches.

Detailed Description

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Conditions

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Adhesive Capsulitis of the Shoulder Suprascapular Nerve Block

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Patients Receiving Suprascapular Nerve Block at the Suprascapular Notch

Group Type ACTIVE_COMPARATOR

Glenohumeral Joint Injection and Suprascapular Nerve Block

Intervention Type PROCEDURE

An intra-articular injection into the glenohumeral joint will be performed using 4 cc of normal saline and 1 cc of betamethasone. Additionally, a suprascapular nerve block will be administered with 5 cc of lidocaine(%2).

Patients Receiving Suprascapular Nerve Block at the Spinoglenoid Notch

Group Type ACTIVE_COMPARATOR

Glenohumeral Joint Injection and Suprascapular Nerve Block

Intervention Type PROCEDURE

An intra-articular injection into the glenohumeral joint will be performed using 4 cc of normal saline and 1 cc of betamethasone. Additionally, a suprascapular nerve block will be administered with 5 cc of lidocaine(%2).

Interventions

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Glenohumeral Joint Injection and Suprascapular Nerve Block

An intra-articular injection into the glenohumeral joint will be performed using 4 cc of normal saline and 1 cc of betamethasone. Additionally, a suprascapular nerve block will be administered with 5 cc of lidocaine(%2).

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients who have had shoulder pain, restricted range of motion (ROM), and night pain for at least 4 weeks

Exclusion Criteria

* Age younger than 35 years or older than 75 years.
* Known allergy to the agents used for injection.
* History of trauma and/or surgery involving the same shoulder.
* Presence of uncontrolled diabetes mellitus and/or hypertension.
* Presence of severe chronic respiratory disease.
* Presence of severe heart failure.
* Administration of intra- or peri-articular steroid injection to the affected shoulder within the past 2 months.
* Radiographic evidence of calcific tendinitis, glenohumeral osteoarthritis, acromioclavicular joint osteoarthritis, or bone fracture.
* Full-thickness rotator cuff tear detected by shoulder ultrasonography.
* History of surgical intervention or recent/past fracture in the ipsilateral upper extremity.
* Presence of complex regional pain syndrome or vascular disease in the ipsilateral extremity.
* Known coagulation disorders.
* Cervical disc pathology causing radiculopathy.
* Presence of inflammatory or malignant diseases.
* History of cerebrovascular disease.
* Presence of mental impairment or severe psychiatric disorders.
* Pregnancy.
Minimum Eligible Age

35 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul University - Cerrahpasa

OTHER

Sponsor Role lead

Responsible Party

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MUSA AVŞAR

medical doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Istanbul University - Cerrahpasa

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Reference Type BACKGROUND
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Reference Type BACKGROUND
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Other Identifiers

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IstanbulUC-MAvsar-01

Identifier Type: -

Identifier Source: org_study_id