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NCT00203268 · ClinicalTrials.gov registry record · NA

A Study Examining the Use of a Migraine Medicine in the Treatment of Two Migraine Attacks in Patients Who Have Increased Skin Sensitivity

A NA study of Migraine, sponsored by Thomas Jefferson University.

Completed
Registry status
NA
Development phase
13
Enrollment target
1
Study location

NCT00203268: Completed NA study of Migraine, sponsored by Thomas Jefferson University.

NCT00203268 is a NA study of Migraine that has completed, run by Thomas Jefferson University. The registered enrollment target is 13 participants, below the 358-participant average among 102 other Migraine trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00203268, a NA study of Migraine, has completed, sponsored by Thomas Jefferson University.

COMPLETED
Registry status
NA
Development phase
13 participants
Enrollment target
1
Study location

Study Summary

This is a research study examining a migraine medicine dihydroergotamine mesylate (DHE-45).It will be used to treat two migraine attacks in subjects who have a history of skin sensitivity associated with their headaches.This skin sensitivity is called cutaneous allodynia (pronounced q-tay-nee-us al-o-din-ee-uh).Cutaneous allodynia is a sensation of pain when a non-noxious stimulus is applied to normal skin. It has been noted in several studies that in subjects with migraine, seventy nine percent of the subjects experienced allodynia on the facial skin on the same side as the headache. It has also been shown that that once allodynia develops, other migraine medicines that would normally be very effective for migraine pain, become much less effective or ineffective. This study will compare the differences,if any, in attacks treated early with this study drug and treated later with the same study drug. It is hoped that that this trial will provide information on the use of DHE-45 in subjects who have cutaneous allodynia. Understanding more about allodynia may help us understand how the pain system works in migraine.

Primary Outcome

Data was collected at 2 hours post treatment to assess pain level. This assessment was done when subjects treated a migraine early (defined as treatment at 2 hours after onset of throbbing pain)and then late (defined as treatment at 4 hours after onset of throbbing pain). The proportion of subjects reporting headache relief at the 2 hour post treatment assessment was determined for each group and then compared.

Conditions Studied

Interventions

  • DRUG dihydroergotamine mesylate

Study Locations (1)

Pennsylvania

  • Jefferson Headache Center - Philadelphia

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2003-12
Est. Completion 2005-03
Phase NA
Thomas Jefferson University

292 total trials

What the finished NCT00203268 record still lists

NCT00203268 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 13 participants, a relatively small participant target, below the 358-participant average among 102 other Migraine trials with a reported enrollment target (96% lower).

The record links to 1 condition, with Migraine appearing as the primary indexed condition, and to 1 intervention - of which dihydroergotamine mesylate is the first listed.

NCT00203268 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00203268 about?

NCT00203268 is a clinical study titled "A Study Examining the Use of a Migraine Medicine in the Treatment of Two Migraine Attacks in Patients Who Have Increased Skin Sensitivity". This is a research study examining a migraine medicine dihydroergotamine mesylate (DHE-45).It will be used to treat two migraine attacks in subjects who have a history of skin sensitivity associated with their headaches.This skin sensitivity is called cutaneous allodynia (pronounced q-tay-nee-us al-...

What is the current status of trial NCT00203268?

This trial is currently completed. It is a NA study. The enrollment target is 13 participants. The study started on 2003-12. Estimated completion is 2005-03.

What conditions does trial NCT00203268 study?

This clinical trial studies the following conditions: Migraine.

What interventions are being tested in trial NCT00203268?

The interventions under investigation include: dihydroergotamine mesylate (DRUG).

Who is sponsoring clinical trial NCT00203268?

This trial is sponsored by Thomas Jefferson University, which has 292 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00203268 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Migraine

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00203268's enrollment target sits among peer trials

13 101st of 102 higher than 2 of 102 other Migraine trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Migraine trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00203268, the US trial registry maintained by the National Library of Medicine. NCT00203268 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.