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Proximal Versus Distal Approach Of Ultrasonographic-Guided Suprascapular Nerve Block (Prospective Randomized Clinical Trial)

Proximal Versus Distal Approach Of Ultrasonographic-Guided Suprascapular Nerve Block (Prospective Randomized Clinical Trial)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004744
Enrollment
56
Registered
2020-02-18
Start date
2019-03-22
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

None listed

Interventions

Procedure/Surgery : All procedures were performed by the treating orthopedic surgeon, who was skilled in the proper technique for US-guided SSNB for both proximal and distal approaches. The patient wa
Canon Medical Systems, Tochigi, Japan) was used. In proximal SSNB group, the SSN was identified in the supraclavicular region described by Siegenthaler et al. The transducer was applied to the side of
). Then, the needle was inserted “in-plane” from lateral to medial direction, and 2-mL of 0.2&#37
Ropivacaine was injected to surround the SSN. In distal SSNB group, the patient was positioned in a same manner as proximal SSNB group. The suprascapular notch was identified as described by Harmon a

Sponsors

Eulji University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The study included patients with adhesive capsulitis, which was defined as follows: insidious onset of shoulder pain and limitations of both active and passive range of motion (forward flexion<100°, external rotation at the side of 0-20°, and internal rotation below the thoracic vertebral level), and no history of major trauma, infection or surgery around the affected shoulder. All patients underwent a thorough history, physical examination, and radiographic imaging studies, including standard plain radiographs and ultrasound imaging scan by the treating orthopedic surgeon.

Exclusion criteria

Exclusion criteria: The exclusion criteria for the study were; (1) patients who diagnosed rotator cuff tear, calcific tendinitis or impingement syndrome by ultrasound imaging, (2) patients with cervical spine disease which could influence peripheral nervous system, (3) patients with previous fracture around shoulder or shoulder surgery, and (4) acute or chronic infection around shoulder.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale

Secondary

MeasureTime frame
American shoulder and elbow surgeons(ASES) score;University of California, Los Angeles(UCLA) score

Countries

Korea, Republic of

Contacts

Public ContactTae Kang Lim

Eulji University Medical Center

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026