NCT06762574Not yet recruiting
"Effect of Low Level Laser Therapy on Neuropathic Pain After Neck Dissection Surgery''
Source: ClinicalTrials.gov · Last updated 7 Jan 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The purpose of the study was to evaluate the effect of Low Level Laser Therapy on neuropathic pain after neck dissection surgery. It was hypothesized that: Low Level Laser Therapy is effective on improving Neuropathic pain post neck dissection surgery .
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 52 (estimated)
- First submitted
- 23 Dec 2024
- Start date
- 6 Jan 2025
- Primary completion date
- 13 Jan 2025
- Lead sponsor
- Cairo University
- Diseases
- Head and neck cancer
- NCT number
- NCT06762574
What you commit to
- Study type: Interventional
- Planned participants: 52
- From 6 Jan 2025 to the primary completion date, 13 Jan 2025
- No sites listed in no 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.
Other illness
- Epilepsy or any psychological
Other
- A wound in the affected area.
- A cervical disk lesion.
- Cervical spine fracture or spondylolisthesis.
- Rheumatoid arthritis.
Who the study is looking for
- Fiftyـtwo patients of both genders with age ranged between 30 to 60 years will participate in this study.
- All patients had neuropathic pain following Unilateral radical neck dissection surgery.
- All patients had history of neuropathic pain involving superficial cervical plexus after unilateral radical neck dissection surgery.
- All patients had moderate or severe pain of tingling,numbness and electric nature following neck dissection surgery. NP confined to the C2-C4 distributions, involves one or more branches of the SCP;especially in the skin overlying lateral neck .
- Informed consent was obtained from every patient enrolled in the trial.
- Moderate to severe pain (VAS score \>4).
Age in the registry: 30 years to 60 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.