Low-level laser light at different wavelengths for cervicogenic headache

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This single-center, single-blinded randomized trial in Lahore will assign adults with cervicogenic headache to one of three LLLT wavelength groups (675 nm 30 mW, 820 nm 200 mW, or a mixed 46-cluster LED probe) with all participants also receiving routine physical therapy. Treatments are delivered three times per week for six weeks (18 sessions) using the Omega XP device, and outcomes include pain (VAS), headache frequency, cervical range of motion, neck disability (NDI), quality of life (SF-36), and forward head posture measured by camera. Participants are followed to 3 and 6 months to assess durability of effects. The trial aims to determine which wavelength option best reduces headache symptoms and improves neck function.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients aged 18-65 years diagnosed with cervicogenic headache based on the International Classification of Headache Disorders (ICHD-3) criteria.
* Persistent headaches for at least 3 months.
* No previous exposure to low-level laser therapy (LLLT).

Exclusion Criteria:

* Patients with other primary headache disorders (e.g., migraine, tension-type headache).
* History of cervical spine surgery.
* Pregnant or lactating women.
* Patients with a history of photosensitivity or taking photosensitizing medications.

Where it's running

• Department of Physiotherapy, Sir Ganga Ram Hospital
  Lahore, Punjab Province, Pakistan Recruiting

Study contacts

• Study coordinator: Arooj Munawar, Ms
• Email: arooj.munawar@uipt.uol.edu.pk
• Phone: 00923214746780

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Comparing two hands-on neck therapies for cervicogenic headache

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• Third occipital nerve pulsed radiofrequency for cervicogenic headache

  This trial will test whether ultrasound-guided pulsed radiofrequency of the third occipital nerve reduces pain in adults with cervicogenic headache who responded to a diagnostic nerve block.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.