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Completed Phase 2 Interventional

Study to Evaluate the Efficacy and Safety of Dronabinol Metered Dose Inhaler (MDI) in Acute Treatment of Migraine Headache

ClinicalTrials.gov ID: NCT00123201

Public ClinicalTrials.gov record NCT00123201. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 26, 2026, 9:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled, Efficacy, Safety and Tolerability Study of Dronabinol MDI in the Acute Treatment of Migraine Headache

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this study is to evaluate the efficacy and safety of dronabinol MDI for the acute treatment of moderate to severe migraine headache.

Study identification

NCT ID
NCT00123201
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Solvay Pharmaceuticals
Industry
Enrollment
Not listed

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2005
Primary completion
Feb 28, 2007
Completion
Feb 28, 2007
Last update posted
Jan 15, 2015

2005 – 2007

United States locations

U.S. sites
29
U.S. states
17
U.S. cities
26
Facility City State ZIP Site status
Site 10 Huntsville Alabama — —
Site 8 Huntsville Alabama — —
Site 11 Tucson Arizona — —
Site 3 Anaheim California — —
Site 6 San Francisco California — —
Site 15 Stockton California — —
Site 26 Melbourne Florida — —
Site 22 New Port Richey Florida — —
Site 18 Orange City Florida — —
Site 27 Pembroke Pines Florida — —
Site 14 Plantation Florida — —
Site 24 Plantation Florida — —
Site 7 St. Petersburg Florida — —
Site 25 Atlanta Georgia — —
Site 12 Chicago Illinois — —
Site 1 Chicago Illinois — —
Site 28 Lexington Kentucky — —
Site 20 Madisonville Kentucky — —
Site 2 Boston Massachusetts — —
Site 19 Omaha Nebraska — —
Site 29 Clementon New Jersey — —
Site 4 Mount Vernon New York — —
Site 9 Raleigh North Carolina — —
Site 23 Fargo North Dakota — —
Site 13 Portland Oregon — —
Site 5 Spartanburg South Carolina — —
Site 16 Bryan Texas — —
Site 17 Colleyville Texas — —
Site 21 Alexandria Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00123201, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 15, 2015 · Synced Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00123201 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →