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Recruiting Phase 4 NCT07022496

NCT07022496 Assessment of Oral Caffeine Intake in Changing the Severity of Acute Migraine Attack Using VAS Score Among Patients Attending Headache and Neurology Outpatients Clinic of Ainshams University Hospitals

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Clinical Trial Summary
NCT ID NCT07022496
Status Recruiting
Phase Phase 4
Sponsor Ain Shams University
Condition Migraine
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2023-04-26
Primary Completion 2025-07

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 60 Years
Study Type INTERVENTIONAL
Interventions
Caffeine (200 mg)triptansNSAID (Nonsteroidal anti-inflammatory drugs)

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.

Phase 4 studies follow an already-approved treatment in real-world conditions to monitor long-term safety and effectiveness.

This trial targets 120 participants in total. It began in 2023-04-26 with a primary completion date of 2025-07.

⚠ 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

Caffeine extracted from green tea to abort acute attack of Migraine

Eligibility Criteria

Inclusion Criteria: Patients suffering from migraine with aura, migraine without aura, episodic, and chronic migraine according to ICHD-3 diagnosis will be legible for the study. Exclusion Criteria: Patients who have history of any cardiac dysrhythmia, hypertension, ischemic heart disease, active peptic ulcer disease, inflammatory bowel disease, obsessive compulsive disorder, pregnancy, breast-feeding, renal failure, hepatic failure, sleep disorder, mental retardation, and history of substance abuse that prevent them from cooperating with us during the study Patients who had headache due to: Cluster headache, trigeminal neuralgia, glossopharyngeal neuralgia, headache secondary to trauma, cranial disorder, vascular disorder, infection, or mass lesion, will also be excluded

Contact & Investigator

Central Contact

Nourhan Nader Elguindy, Masters degree

✉ nourhanelguindy@gmail.com

📞 00201128215952

Frequently Asked Questions

Who can join the NCT07022496 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 60 Years, studying Migraine. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT07022496 trial and what does that mean for participants?

Phase 4 studies are conducted after a treatment has been approved. They monitor long-term safety and real-world effectiveness in a broader patient population.

Is NCT07022496 currently recruiting?

Yes, NCT07022496 is actively recruiting participants. Contact the research team at nourhanelguindy@gmail.com for enrollment information.

Where is the NCT07022496 trial being conducted?

This trial is being conducted at Cairo, Egypt.

Who is sponsoring the NCT07022496 clinical trial?

NCT07022496 is sponsored by Ain Shams University. The trial plans to enroll 120 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: September 2026  ·  Data Methodology