The Impact of Cervical Radiculopathy on Functionality in Patients Undergoing Rotator Cuff Repair
NCT ID: NCT07001566
Last Updated: 2025-06-03
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.
RECRUITING
50 participants
OBSERVATIONAL
2025-03-20
2025-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Study topic: The participants of the study were selected from patients who underwent rotator cuff repair at the Orthopedics and Traumatology clinic of Kartal Dr. Lütfi Kırdar City Hospital between 2018 and 2023. The first group consisted of patients without cervical radiculopathy, while the second group included patients with a previously diagnosed cervical radiculopathy. The study will examine the effect of the presence of cervical radiculopathy on functional outcomes and quality of life in patients who underwent rotator cuff repair.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Upper Extremity Dysfunction in Patients With Cervical Radiculopathy
NCT06923085
Assessment of Upper Extremity Proprioception in Patients With Cervical Radiculopathy
NCT07319156
Functional Limitation, Pain and Quality of Life in Patients With Cervical Spondylotic Radiculopathy
NCT06001359
Acute Effect of Neural Mobilization in Cervical Radiculopathy: A Randomized Controlled Study
NCT05887427
The Investigation of Thoracic Spinal Curvature and Mobility in Subjects With and Without Neck Pain: Cut-off Points
NCT02424058
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Cervical radiculopathy occurs when a nerve root in the spine is compressed or blocked, leading to pain that can radiate beyond the neck, to the arm, chest, shoulders, and upper back. Common symptoms of compression include muscle weakness and impaired deep tendon reflexes. These deficiencies can worsen over time, leading to a decline in quality of life and daily function. While most symptoms can be treated with supportive care, more severe functional loss may require rehabilitation or surgery. Any condition that causes compression or irritation of the spinal nerve root can lead to radicular symptoms. In younger patients, typically in their third and fourth decades, disc trauma and herniation are the most common causes of compression. As age increases, the cause tends to be degenerative. Disc degeneration is the most common cause in the fifth and sixth decades. In the seventh decade, it results from arthritic changes due to foraminal narrowing. Cervical radiculopathies are less frequently seen than lumbar radiculopathies, occurring in approximately 85 per 100,000 people. The C7 nerve root is most frequently affected, with more than half of all cases involving this level. About a quarter of cases involve the C6 nerve root. The C1 to C5 and C8 nerve roots are less affected. Risk factors for developing radicular disease include manual labor such as heavy lifting, driving, or operating vibrating equipment (Magnus, 2024).
Rotator cuff syndrome, also known as rotator cuff tear, is an injury that affects the shoulder, causing pain and inability to use the arm due to the tearing of the muscles and tendons in the rotator cuff. Rotator cuff syndrome can be partial or complete, and is typically caused by injury, trauma, or degeneration. Rotator cuff surgery is rapidly advancing, with most progress driven by improvements in arthroscopic techniques. Generally, functional outcomes are satisfactory. Tendon healing is associated with better results, especially with more strength. Therefore, the best candidates for surgery are those with lesions that have a high likelihood of recovery. Factors associated with recovery include being under 65 years old, having had a recent tear, no history of smoking, having an acromiohumeral distance greater than 6 mm, and a Goutallier fatty degeneration grade of less than 2 in the infraspinatus or subscapularis muscles.
A retrospective cohort study investigated the relationship between cervical spine and rotator cuff pathology and confirmed the existence of this relationship.
In a previous study, it was shown that patients with a history of cervical spine issues who underwent shoulder surgery had lower postoperative functional outcomes, lower satisfaction, and higher rates of postoperative complications requiring surgical revision, compared to patients without cervical spine issues. Another study, focusing on a cohort of patients who underwent shoulder surgery, showed that the short-term postoperative outcomes of patients with cervical spine pathology were significantly lower compared to the functional outcomes of patients without cervical spine pathology.
The sample size was calculated using the G\*Power 3.1.9.7 program. The logistic regression test was used, with α error set at 0.20 and 80% power. The odds ratio value from Zhang et al.'s (2015) study, titled The Association Between Cervical Spine Pathology and Rotator Cuff Dysfunction, was used as a reference for patients diagnosed with cervical pathology who developed rotator cuff injury or underwent surgery within a five-year period. Based on this value, the required sample size to achieve 80% power was calculated to be 78 participants.
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.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patient's who has cervical radiculopathy
There will be only done assessment.
There was no intervention. Only assessment procedure will be performed.
There was no intervention. Only assessment procedure will be performed.
Patient's who has not cervical radiculopathy
There will be only done assessment.
There was no intervention. Only assessment procedure will be performed.
There was no intervention. Only assessment procedure will be performed.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
There was no intervention. Only assessment procedure will be performed.
There was no intervention. Only assessment procedure will be performed.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients under the age of 65
Exclusion Criteria
* Patients with a history of cervical spine surgery
* Patients with any neurological disorders
* Patients with a history of pathological fractures
* Patients with oncological diseases
* Patients with a history of infection
* Patients who were deceased at the time of retrospective screening
41 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Biruni University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Guzin Kaya Aytutuldu
Assistant Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kartal Lütfi Kırdar City Hospital
Istanbul, Istanbul, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Biruni University PTR
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.