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Recruiting NCT06943625

NCT06943625 Combined Effects of Green Light and Transcranial Direct Current Stimulation in Migraine Patients.

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Clinical Trial Summary
NCT ID NCT06943625
Status Recruiting
Phase
Sponsor Riphah International University
Condition Migraine
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2025-04-24
Primary Completion 2026-03-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
tDCSGreen lightmedicine

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

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 40 participants in total. It began in 2025-04-24 with a primary completion date of 2026-03-31.

⚠ 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

According to the Global Burden of Disease (GBD) study, headache disorders are among the most prevalent and disabling conditions worldwide, with estimated 1-year prevalence of migraine (22.5%) in Pakistan, considerably higher than the global 1-year prevalence of 15%. The treatment options comprise such as lifestyle modifications, behavioral therapy, medication such as nonsteroidal anti-inflammatory drugs (NSAIDs), beta blockers, calcium channel blockers, antiepileptic drugs or antibodies against calcitonin gene-related peptide (CGRP) or its receptor, and neuromodulation. One of the non-invasive neuromodulation technique is used in migraine patients .i.e., transcranial direct current stimulation (tDCS), tDCS is a promising method for migraine treatment delivering a low-intensity current through the scalp by means of electrodes to modulate the state of polarization of the cerebral cortex; depending on the polarity of the electrical stimulation, tDCS can be either anodal(excitatory) or cathodal(inhibitory). Neuromodulation by tDCS is thought to follow Hebbian Theory ("neurons that fire together, wire together"). If presynaptic and postsynaptic neurons are both active, the result is synaptic strengthening; if one or both are inactive, no change occurs. The literature reported significant reduction in migraine days when applying tDCS to the occipital cortex, primary motor cortex, or the dorsolateral prefrontal cortex. The advantages of tDCS treatment are its relatively low cost compared to other neurostimulator methods, safety and generally mild side effects.

Eligibility Criteria

Inclusion Criteria: * Episodic migraine or chronic migraine according to the International Headache Society * An average headache pain intensity of migraine episodes of ≥5 at numeric pain scale (NPS) over the 4 weeks prior to enrolling in the study Exclusion Criteria: * Mental illness * Photophobic individual * Presence of shunt and/or implant at the cranial region * Brain tumors * Wound at skull

Contact & Investigator

Central Contact

Sufia Omar, DPT

✉ sofo.umar97@gmail.com

📞 00923341827272

Principal Investigator

Mirza Obaid Baig, MSPT

PRINCIPAL INVESTIGATOR

Riphah International University

Frequently Asked Questions

Who can join the NCT06943625 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Migraine. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06943625 currently recruiting?

Yes, NCT06943625 is actively recruiting participants. Contact the research team at sofo.umar97@gmail.com for enrollment information.

Where is the NCT06943625 trial being conducted?

This trial is being conducted at Rawalpindi, Pakistan, Rawalpindi, Pakistan.

Who is sponsoring the NCT06943625 clinical trial?

NCT06943625 is sponsored by Riphah International University. The principal investigator is Mirza Obaid Baig, MSPT at Riphah International University. The trial plans to enroll 40 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology