Improvement of Range of Motion in Frozen Shoulder in Breast Cancer Survivors
NCT ID: NCT04640220
Last Updated: 2022-01-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
28 participants
INTERVENTIONAL
2020-10-26
2021-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Correlation Between Ultrasonography Finding and Shoulder Range of Motion in Stroke Patients
NCT04738253
Proprioceptive Neuromuscular Facilitation Techniques in Patients With Adhesive Capsulitis
NCT04878848
The Study of Different Treatment Programs for Patients With Frozen Shoulder
NCT01249040
Comparison of the Effectiveness of Stretching and Strengthening Exercises in Patients With Frozen Shoulder
NCT06469502
Scientifically Merged Acupuncture and Robot-assisted Technology (SMART) for Rehabilitation of Frozen Shoulder Syndrome: Second-year Project-Comparison of Robot and Conventional Physiotherapy (Including Preliminary Test on Healthy Volunteers)
NCT02206542
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Adhesive capsulitis in breast cancer survivors
Intra-articular steroid injection
Intra-articular steroid injection
Ultrasound-guided Gleno-humeral joint steroid (Triamcinolone 40mg with 0.5% lidocaine ) injection
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Intra-articular steroid injection
Ultrasound-guided Gleno-humeral joint steroid (Triamcinolone 40mg with 0.5% lidocaine ) injection
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients with shoulder pain and limited range of motion
Exclusion Criteria
* Bilateral shoulder pain patient
* Patients with uncontrolled diabetes
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Yeungnam University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dong Gyu Lee
Assistant professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Dong Gyu Dong Gyu, M.D., Ph.D.
Role: PRINCIPAL_INVESTIGATOR
College of medicine, Yeungnam University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Yeungnam University Hospital
Daegu, , South Korea
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2020-07-064-002
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.