Prevention of Menstrual Migraines: Using Frovatriptan or Placebo During Hormone Free Intervals

Bleeding Clinical Trial

— MAM  

Official title:

Prevention of Menstrual Migraines: Effects of Continuous Oral Contraceptives to Combination With Prophylactic Frovatriptan Use During Hormone Free Intervals

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00700128
• Other study ID #: 060714
• Status: Completed
• Phase: N/A
• First received: June 17, 2008
• Last updated: July 22, 2011
• Start date: June 2008
• Est. completion date: January 2010

Study information

• Verified date: July 2011
• Source: Scott and White Hospital & Clinic
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal GovernmentUnited States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This study will examine the combined effects of a continuous oral contraceptive (OC) regimen with supplemental frovatriptan therapy on headache severity and occurrence in subjects with documented Menstrually Associated Migraines (MAM). The subjects enrolling in the study will have cyclic menses either due to spontaneous ovulation or use of cyclic hormonal contraception (pill, patch, or ring). Enrolled subjects will start a continuous OC regimen following two baseline menstrual cycles. If breakthrough bleeding/spotting (BTB/BTS) occurs, the subject will institute a 4-day hormone-free interval (HFI). In an attempt to prevent/lessen the severity of headache during the HFI, subjects will be randomized to prophylactic administration of a triptan or placebo during this period. If no BTB/BTS occurs after 80 days of continuous pills, the subject will institute a 4-day HFI during which they will be randomized into triptan or placebo groups.

The purpose of this research study is to examine the effects of continuous oral contraceptive pills and frovatriptan on headaches that occur around the time of your period. Many woman take continuous oral contraceptive pills (OC) and when OCs are stopped they may get headaches. This study will look if taking frovatriptan around the time of the period will affect the headache, and how it will be affected. Frovatriptan is an FDA approved drug for migraine headaches.

This study is a prospective pilot trial.The study will last approximately 35-39 weeks.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: January 2010
• Est. primary completion date: January 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Woman may be on birth control pill (OC), patch or NuvaringTM (vaginal ring) taken in the traditional 21/7 or 24/4 manner, which means ever month they have a period. If they are taking it continuously (without a period), you must be willing to take your birth control 24/4 (4 days taking hormone free interval, HFI) for 2 months.

• If you are not on OCs, patch or NuvaringTM you must have a period every 21-40 days.

• You must not want to get pregnant for 12 months.

• Women have headaches around the time of their period.

Exclusion Criteria:

• BMI > 38

• If you smoke and are age 35 years old or greater or if are under 35 years old and smoke over 10 cigarettes a day

• If you have or had an aura with your headaches (An aura is a temporary sensation, like bright lights that come before you experience the headache.)

• Headaches are not occurring during the time of your period.

• Blood Pressure > 140/90 or you take more than a single antihypertensive medication (excluding diuretics) and are age 40 or greater.

• Contraindications to combination estrogen/progestin hormonal contraception.

• Desire to become pregnant in the next 12 months.

• Refuse to avoid any ergot-based medication, triptan medication or isometheptene/midrin during their hormone free interval or the one day before the hormone free interval

• Stroke

• Breast Cancer

• Blood clots in your legs, lung or anywhere else in your body

• Diabetes mellitus

• Heart attack

• Liver disease

• Lupus Erythematosus

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Bleeding
• Migraine Disorders
• Migraines
• Spotting

Intervention

Drug:
• frovatriptan
Frovatriptan 2.5 mg or placebo given Bid starting on the last day of OC before taking the 4 day HFI. They will take a total of 10 pills max per HFI.
• frovatriptan
frovatriptan 2.5 mg bid or placebo starting on the last day of OC and continuing during the 4 day HFI.
• placebo
placebo

Locations

Country	Name	City	State
United States	Scott & White Memorial Hospital	Temple	Texas

Sponsors (2)

Lead Sponsor	Collaborator
Scott and White Hospital & Clinic	Endo Pharmaceuticals

Country where clinical trial is conducted

United States, 

References & Publications (1)

1. Lipton RB, Bigal ME, Diamond M, Freitag F, Reed ML, Stewart WF; AMPP Advisory Group. Migraine prevalence, disease burden, and the need for preventive therapy. Neurology 2007; 68(5):343-9. 2. Tozer BS, Boatwright EA, David PS, Verma DP, Blair JE, Mayer AP, Files JA. Prevention of migraine in women throughout the life span. Mayo Clin Proc. 2006;81(8):1086-91. 3. Macgregor EA. Menstrual migraine: a clinical review. Journal of family planning and reproductive health care, 2007. 33(1), 36-47. 4. Brandes JL. The influence of estrogen on migraine: a systematic review. JAMA, 2006; 295(15):1824-30. 5. Sulak PJ, Scow RD, Preece C, Riggs MW, Kuehl TJ. Hormone withdrawal symptoms in oral contraceptive users. Obstet Gynecol 2000; 95:261-6. Sulak P, Willis S, Kuehl T, Coffee A, Clark J. Headaches and oral contraceptives: impact of eliminating the standard 7-day placebo interval. Headache. 2007;

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Comparing baseline menstrually associated migraines (MAMs)to headache occurrence and severity after the implementation of continuous OC therapy.		24 weeks	No
Secondary	Compare amount of bleeding and spotting within subjects in relation to duration of extended oral contraceptive pills (OCP) use for those previously using the 21/7 day regimen and those initiating OCP use directly from spontaneous cycling.		24 weeks	No

External Links

•   Scott & White Memorial Hospital Clinical Trials