Diphenhydramine for Acute Migraine
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ClinicalTrials.gov Identifier: NCT01825941 |
Recruitment Status :
Completed
First Posted : April 8, 2013
Results First Posted : June 8, 2018
Last Update Posted : July 31, 2018
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Migraine | Drug: metoclopramide Drug: diphenhydramine Drug: placebo | Phase 4 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 208 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | Diphenhydramine as Adjuvant Therapy for Acute Migraine. A Randomized Trial. |
Study Start Date : | April 2013 |
Actual Primary Completion Date : | December 2014 |
Actual Study Completion Date : | December 2014 |

Arm | Intervention/treatment |
---|---|
Active Comparator: Metoclopramide + Diphenhydramine
Metoclopramide 10 milligrams + Diphenhydramine 50 milligrams, administered as an intravenous drip over 15 minutes
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Drug: metoclopramide
10 milligrams, administered intravenously over 15 minutes
Other Name: Reglan Drug: diphenhydramine 50 milligrams, administered intravenously over 15 minutes
Other Name: Benadryl |
Placebo Comparator: Metoclopramide + placebo
Metoclopramide 10mg + placebo, administered intravenously over 15 minutes
|
Drug: metoclopramide
10 milligrams, administered intravenously over 15 minutes
Other Name: Reglan Drug: placebo |
- Number of Participants With Sustained Headache Relief Assessed by Self-evaluation [ Time Frame: up to 2 hours in Emergency Department, 48 hours after discharge from Emergency Department ]Sustained headache relief is defined as achieving a headache level of "mild" or "none" within two hours and maintaining a level of "mild" or "none" for 48 hours. Patient self-evaluated pain level is solicited every half hour for two hours in the Emergency Department and then by telephone 48 hours after discharge from emergency department

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Ages Eligible for Study: | 21 Years to 64 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Acute migraine headache
- Present to our emergency room in the Bronx, NY for treatment of migraine headache
Exclusion Criteria:
- Temperature > 100.3 F
- Pheochromocytoma
- Seizure disorder
- Parkinson's disease
- Use of monoamine oxidase (MAO) inhibitors
- Use of anti-rejection transplant medications
- Use of potassium supplements
- Use of pramlintide

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01825941
United States, New York | |
Montefiore Medical Center | |
Bronx, New York, United States, 10467 |
Principal Investigator: | Benjamin W Friedman | Montefiore Medical Center |
Responsible Party: | Benjamin W. Friedman, MD, Associate professor of Emergency Medicine, Montefiore Medical Center |
ClinicalTrials.gov Identifier: | NCT01825941 |
Other Study ID Numbers: |
13-02-071 |
First Posted: | April 8, 2013 Key Record Dates |
Results First Posted: | June 8, 2018 |
Last Update Posted: | July 31, 2018 |
Last Verified: | July 2018 |
migraine headache metoclopramide diphenhydramine |
Migraine Disorders Headache Disorders, Primary Headache Disorders Brain Diseases Central Nervous System Diseases Nervous System Diseases Diphenhydramine Promethazine Metoclopramide Sleep Aids, Pharmaceutical Hypnotics and Sedatives Central Nervous System Depressants Physiological Effects of Drugs Anesthetics, Local Anesthetics |
Sensory System Agents Peripheral Nervous System Agents Antiemetics Autonomic Agents Gastrointestinal Agents Histamine H1 Antagonists Histamine Antagonists Histamine Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Anti-Allergic Agents Antipruritics Dermatologic Agents Dopamine D2 Receptor Antagonists Dopamine Antagonists |