NCT06555913Completed
Maitland Mobilization and Scapular Stabilization Shoulder Dysfunction
Maitland Mobilization and Scapular Stabilization Exercises on Shoulder Dysfunction Post Neck Dissection Surgeries
Source: ClinicalTrials.gov · Last updated 20 Aug 2024
Brief summary (registry, in English)
Sixty patients from both genders suffering from shoulder disability post unilateral NDS (modified radical, selective) will participate in this study. Their ages will be ranged from 30 to 50 years. They will be selected randomly from Damanhur Oncology center, El-Behira, Egypt. They will be randomly distributed into three equal groups (each group 20 patients).
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 60 (actual)
- First submitted
- 13 Aug 2024
- Start date
- 1 Nov 2023
- Primary completion date
- 1 Jun 2024
- Lead sponsor
- Cairo University
- Diseases
- Head and neck cancer
- NCT number
- NCT06555913
What you commit to
- Study type: Interventional
- Participants enrolled: 60
- From 1 Nov 2023 to the primary completion date, 1 Jun 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Recent fracture or surgery to the shoulder.
Other illness
- Adhesive capsulitis secondary to Diabetes mellitus or fractures.
- Neurological disorder.
- Epilepsy or any psychological disorders.
- The presence of residual local-regional cancer or distant metastases to other regions.
Other
- Subjects with rotator cuff tears or other •shoulder ligament injuries.
- Recurrent shoulder dislocation.
- Reflex sympathetic dystrophy.
Who the study is looking for
- Patients' age will be ranged between 30-50 years.
- Both genders will participate in this study.
- All patients suffering from shoulder pain and disability following unilateral modified radical NDS or selective NDS.
- All patients will begin the treatment program from 1 to 3 months after NDS.
- All patients will have limited ROM of shoulder flexion, abduction, external rotation.
- All patients enrolled to the study will have their informed consent.
Age in the registry: 30 years to 50 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Faculty of Physical Therapy Coordinator of this site? Confirm its status | Giza | Egypt | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.