NCT07196800 Effect of Dose Variations of High-Power Laser Therapy on Patients With Nonspecific Cervical Pain
| NCT ID | NCT07196800 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Deraya University |
| Condition | Neck Pain |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2025-03-10 |
| Primary Completion | 2025-11-10 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2025-03-10 with a primary completion date of 2025-11-10.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Nonspecific neck pain, defined as pain without a specific underlying pathology, is a common musculoskeletal disorder that affects a significant proportion of the global population. Neck pain often results in considerable discomfort and functional limitations, impacting individuals' quality of life and ability to perform daily tasks. Estimates suggest that up to 30% of adults experience neck pain annually. The condition ranks among the top causes of disability worldwide, contributing to substantial personal and societal burdens, including lost work productivity and increased healthcare costs.
Eligibility Criteria
Inclusion Criteria: * unilateral or bilateral CNP * Experiencing moderate to severe neck pain, defined as a Visual Analog * Scale (VAS) score of ≥4. * Cervical Range of Motion (ROM) Limitation: Documented restriction in cervical ROM compared to normal values for age and gender, to ensure the condition's impact on functional mobility * Patients agreed not to take any medication(anti-inflammatories, analgesics, or muscle relaxants) throughout the course of the study or receive any type of treatment for neck pain Exclusion Criteria: * Previous Cervical Surgery: Patients with a history of cervical spine surgery will be excluded to eliminate potential influences from post-surgical changes on the outcomes * Diagnosed with cervical disc prolapse as confirmed by clinical evaluation and imaging studies (MRI or CT scans). * History of malignancy in the cervical region or other serious medical conditions. * Severe comorbidities that may affect treatment outcomes (e.g., uncontrolled diabetes, cardiovascular diseases). * Pregnancy or lactation.
Frequently Asked Questions
Who can join the NCT07196800 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 40 Years, studying Neck Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07196800 currently recruiting?
Yes, NCT07196800 is actively recruiting participants. Visit ClinicalTrials.gov or contact Deraya University to inquire about joining.
Where is the NCT07196800 trial being conducted?
This trial is being conducted at Minya, Egypt.
Who is sponsoring the NCT07196800 clinical trial?
NCT07196800 is sponsored by Deraya University. The trial plans to enroll 60 participants.