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Ginger Capsules for the Prophylactic Treatment of Migraine

F

Federal University of Minas Gerais

Status

Completed

Conditions

Migraine

Treatments

Other: Cellulose
Other: Extract of ginger

Study type

Interventional

Funder types

Other

Identifiers

NCT02570633
CAAE 28236814.3.0000.5149

Details and patient eligibility

About

The main objective of the study is to evaluate ginger efficacy as an prophylactic treatment of migraine.

Full description

Patients with the diagnosis of migraine according to the IHS criteria will receive capsules of 200 mg of ginger extract (5% active ingredient) or placebo (cellulose) to be taken three times a day for 12 weeks.

Enrollment

107 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged between 18 and 60 years old;
  • Migraine diagnosis;
  • Agree to sign the informed consent.

Exclusion criteria

  • Patients with headaches not characterized as migraine;
  • Pregnant or lactating women;
  • Fertile and sexually active women who do not use contraception;
  • Abuse of painkillers, alcohol or other drugs;
  • People with hypersensitivity to ginger compounds;
  • People with severe neurological diseases (e.g. epilepsy)
  • People in use of anticoagulant drugs.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

107 participants in 2 patient groups, including a placebo group

Extract of ginger
Experimental group
Description:
Migraine patients (both genders) will receive capsules of 200 mg of ginger extract (5% gingerols) to be taken three times a day for 12 weeks.
Treatment:
Other: Extract of ginger
Cellulose
Placebo Comparator group
Description:
Migraine patients (both genders) will receive capsules of 200 mg of placebo (cellulose) to be taken three times a day for 12 weeks.
Treatment:
Other: Cellulose

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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