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Low-Dose Naltrexone and Acetaminophen Combination and Its Components in the Acute Treatment of Migraine | Clinical Trials | Clareo Health

COMPLETEDPHASE2

Low-Dose Naltrexone and Acetaminophen Combination and Its Components in the Acute Treatment of Migraine

A Clinical Trial to Assess a Single Dose of Low-Dose Naltrexone and Acetaminophen Combination and Its Components in the Acute Treatment of Migraine

NCT03061734•Allodynic Therapeutics, Inc

View on ClinicalTrials.gov

Summary

The study consists of a screening visit, out-patient treatment of a moderate or severe migraine attack with a single dose of the study medication within 8 weeks, and End-of-Study Visit 2-7 days after dosing.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•1. Male or female 18 years of age or older.
•2. History of migraine with or without aura according to the International Classification of Headache Disorders (ICHD)-3rd edition (beta version) for at least one-year with first migraine prior to age 50.
•3. Migraine-associated nausea with ≥half of migraine attacks.
•4. 2 - 8 migraines per month in each of the previous 3 months.
•5. The patient is able to complete study questionnaires, comply with the study requirements and restrictions, and willing to provide written informed consent and authorize HIPAA.
•6. The female patient who is premenopausal or postmenopausal less than 1 year, or have not had surgical sterilization (i.e., tubal ligation, partial or complete hysterectomy) must have a negative urine pregnancy test, be non-lactating, and commit to using adequate and reliable contraception throughout the study (e.g., barrier with additional spermicidal, intra-uterine device, hormonal contraception). The male patient must be surgically sterile or commit to the use of 2 different methods of birth control during the study and for 28 days after taking the study drug.

Exclusion Criteria

•1. The patient in the opinion of the investigator, may have medication-overuse headache pain (as defined by ICHD - 3 beta criteria for medication-overuse headache), (analgesic, opioid, ergotamine or triptan overuse) during the 3 months preceding screening.
•2. The patient in the opinion of the investigator has chronic migraine (as defined by ICHD - 3 beta criteria for chronic migraine).
•3. History of cluster headache or neurologically complicated migraine (hemiplegic, basilar, retinal, ophthalmoplegic migraine).
•4. Initiation or change in medications with possible migraine prophylactic effects during 3 months before inclusion into the trial (E.g., calcium channel blockers, tricyclic antidepressants, beta-blockers, selective serotonin re-uptake inhibitors (SSRIs), serotonin-norepinephrine re-uptake inhibitors (SNRIs), or Botox).
•5. Any concurrent medical or psychiatric condition, this includes, but is not limited to chronic unstable debilitating diseases, significant renal or hepatic impairment.
•6. A history within the previous 3 years of abuse of any drug, prescription, illicit, or alcohol.
•7. The Female patient is pregnant or breast-feeding. The Male patient is not practicing 2 different methods of birth control with their partner during the study, and for 28 days after the investigational drug last dose or will not remain abstinent during the study, and for 28 days after the last dose.
•8. Use of opiates or barbiturates more than 3 days per month.
•9. Known-hypersensitivity reaction to any of the components of the investigational drug.
•10. Consumption of analgesic medication for other conditions on a regular basis, (nonsteroidal anti-inflammatory drugs, or acetaminophen, or muscle relaxants).
+2 more criteria

Locations (1)

Annette C. Toledano MD

North Miami, Florida, United States

Key Dates

Start Date

February 18, 2017

Primary Completion Date

February 8, 2018

Completion Date

February 8, 2018

Last Updated

April 14, 2021

Enrollment

ACTUAL participants

Conditions

Migraine With or Without Aura

Interventions

Naltrexone and Acetaminophen

DRUG

Naltrexone and Acetaminophen-High Dose

DRUG

Naltrexone Alone (regular dose)

DRUG

Acetaminophen Alone

DRUG

Matching Placebo

DRUG

The Preventive Treatment of Migraine With Low-Dose Naltrexone and Acetaminophen Combination

NCT03194555

Migraine With or Without Aura

View study

COMPLETEDPHASE3

Eletriptan vs Sumatriptan: A Double-blind, Placebo-controlled, Multiple Migraine Attack Study

NCT01986088

Migraine With or Without Aura

View study

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 14, 2021Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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