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A prospective study of selective nerve block and individualized rehabilitation for the frozen shoulder

A prospective study of selective nerve block and individualized rehabilitation for the frozen shoulder - A prospective study of selective nerve block and individualized rehabilitation for the frozen shoulder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000040855
Enrollment
120
Registered
2020-06-23
Start date
2020-06-25
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Frozen shoulder

Interventions

selective nerve block(Once a week for up to 4 weeks) intra-articular injection(Once a week for up to 4 weeks)

Sponsors

Department of Anesthesiology and Perioperative Medicine,Tohoku University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with frozen shoulders diagnosed as frozen stage. (1) Frozen shoulder diagnostic criteria 1. Shoulder pain and contracture of the shoulder joint in more than one direction (flexion 90 degrees or less, external rotation 30 degrees or less, or internal sacrum or less) 2. Excludes organic diseases such as calcareous rotator cuff inflammation and rotator cuff tear using X-ray/MRI/echo. (2) Diagnostic criteria for frozen stage 1. Within 3 months of onset. 2. Assessed pain intensity with visual analog scale is less than 30. 3. The contracture remains.

Exclusion criteria

Exclusion criteria: (1) Patients with a history of trauma or other shoulder disease (2) Patients with a history of diabetes (3) Patients with a history of thyroid disease (4) Patients with mental illness (5) Patients who are allergic to local anesthetics (6) Patients participating in other studies (7) Patients who are not qualified by the doctor in charge

Design outcomes

Primary

MeasureTime frame
Changes in Quick DASH score (JSSH version) up to 8 weeks after treatment intervention.

Secondary

MeasureTime frame
Shoulder range of motion, pain intensity (visual analog scale), analgesic usage, treatment satisfaction (visual analog scale), muscle elasticity.

Countries

Japan

Contacts

Public ContactNorifumi Yoshida

Tohoku University School of Medicine Department of Anesthesiology and Perioperative Medicine

anes@med.tohoku.ac.jp022-717-7321

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026