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Does Ultrasound-guided Suprascapular Nerve Block Provide Additional Benefit Over Traditional Rehabilitation Program for Patients With Chronic Shoulder Pain

Does Ultrasound-guided Suprascapular Nerve Block Provide Additional Benefit

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02776865
Acronym
2015/8/1
Enrollment
60
Registered
2016-05-18
Start date
2015-10-31
Completion date
Unknown
Last updated
2016-05-18

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

Conditions

Suprascapular Nerve Block

Keywords

suprascapular nerve block

Brief summary

This study was conducted to compare the efficacy of hydrodilatation with hyaluronic acid under ultrasonographic guidance plus physical therapy (PT) with that of PT alone for treating adhesive capsulitis

Interventions

DRUGsuprascapular nerve block

4ml 2% xylocaine

OTHERphysical therapy

patient received traditional physical therapy, including therapeutic exercise and stretch exercise

Sponsors

Taipei Veterans General Hospital, Taiwan
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. chronic shoulder pain with duration of complaints more than 3 months 2. diagnosis of frozen shoulder or rotator cuff disorder

Exclusion criteria

1. other conditions involving the shoulder ( rheumatoid arthritis, Hill-Sachs lesions,osteoporosis, or malignancies in the shoulder region); 2. neurologic deficits affecting shoulder function in normal daily activities; 3. shoulder pain caused by cervical radiculopathy 4. a history of drug allergy to xylocaine 5. pregnancy or lactation; 6. received injection into the affected shoulder during the preceding 3 months

Design outcomes

Primary

MeasureTime frameDescription
change in constant shoulder scoreat 4, 12 wkthe total constant score ranges from 0 to 100 points, with higher scores indicative of better function. The score is divided into four sections: pain, activity of daily living, ROM and strength

Secondary

MeasureTime frameDescription
change in pain intensityat 4, 12 wkpain intensity was measured by visual analog scale.
change in Shoulder Pain And disability indexat 6, 12 wkThe Shoulder Pain and Disability Index (SPADI) is a self-administered questionnaire that consists of two dimensions, one for pain and the other for functional activities. The pain dimension consists of five questions regarding the severity of an individual's pain. Functional activities are assessed with eight questions designed to measure the degree of difficulty an individual has with various activities of daily living that require upper-extremity use. The SPADI takes 5 to 10 minutes for a patient to complete and is the only reliable and valid region-specific measure for the shoulder.
change in glenohumeral joint range of motionat 4, 12 wkShoulder flexion, abduction, external rotation and internal rotation were measured with goniometer with patient in supine position.

Countries

Taiwan

Contacts

Primary ContactJia chi Wang, MD
jcwang0726@gmail.com

Outcome results

None listed

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