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MigrainePhase 2NCT00781456

A Multicenter Study to Evaluate the Efficacy of a 91-Day Extended Cycle Oral Contraceptive for Menstrually-Related Migraine Headaches

A Phase 2 study testing 91-day Levonorgestrel Oral Contraceptive in people with Migraine, run by Duramed Research at 22 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study is being conducted to evaluate the efficacy of a 91-day extended cycle oral contraceptive compared to placebo for decreasing the frequency and severity of menstrually-related migraine headaches. Read more about this study

Who is it for?
Ages 18 to 34 years, women only
Conditions the study is for
Migraine
What is being tested?
91-day Levonorgestrel Oral Contraceptive
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
109 participants
Where
22 sitesUnited States
Study dates
Jan 2009to Aug 2011
Phase
Phase 2
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 34 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • Premenopausal, non-pregnant, non-lactating
  • History of migraine headaches without aura for at least 6 months
  • History of migraine headaches associated with menstruation
  • Others as directed by FDA-approved protocol

Who cannot join

  • History of migraine headaches with aura or focal neurological symptoms
  • Any contraindication to the use of oral contraceptives
  • Others as dictated by FDA-approved protocol

Trial locations and contacts

22 sites in 1 country.

22 sites in 1 country

United States22 sites
  • Teva Investigational Site

    Columbia, South Carolina, 29201

  • Duramed Investigational Site

    Dallas, Texas, 75234

  • Duramed Investigational Site

    Edison, New Jersey, 08817

  • Teva Investigational Site

    Hilton Head, South Carolina, 29926

  • Teva Investigational Site

    Houston, Texas, 77054

  • Teva Investigational Site

    La Mesa, California, 91942

  • Teva Investigational Site

    Medford, Oregon, 97504

  • Teva Investigational Site

    Memphis, Tennessee, 38120

  • Duramed Investigational Site

    New York, New York, 10022

  • Duramed Investigational Site

    Philadelphia, Pennsylvania, 19114

  • Duramed Investigational Site

    San Antonio, Texas, 78258

  • Duramed Investigational Site

    San Diego, California, 92108

  • Teva Investigational Site

    San Diego, California, 92123

  • Duramed Investigational Site

    San Francisco, California, 94109-4841

  • Teva Investigational Site

    Savannah, Georgia, 31406

  • Duramed Investigational Site

    Seattle, Washington, 98105

  • Teva Investigational Site

    Tulsa, Oklahoma, 74105

  • Teva Investigational Site

    Uniontown, Pennsylvania, 15401

  • Duramed Investigational Site

    Virginia Beach, Virginia, 23454

  • Duramed Investigational Site

    Washington D.C., District of Columbia, 20036

  • Duramed Investigational Site

    West Palm Beach, Florida, 33409

  • Teva Investigational Site

    Winston-Salem, North Carolina, 27103

Other trials in United States

About this study

Official title: A Multicenter, Randomized, Double-Blind Study to Evaluate the Efficacy of DR-105 Compared to Placebo For the Management of Menstrually-Related Migraine Headaches.

This study is being conducted to evaluate the efficacy of a 91-day extended cycle oral contraceptive compared to placebo for decreasing the frequency and severity of menstrually-related migraine headaches.

Conditions
Migraine
Being tested
91-day Levonorgestrel Oral Contraceptive, Placebo
Keywords
Migraine headache, menstrual, oral contraceptive, Menstrually-Related Migraine Headache
Medical subject headings
Migraine Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 91-day Levonorgestrel Oral ContraceptiveDrug

    Also called Seasonique, DR-105

    91-day treatment consisting of 84 blue combination tablets containing 150 µg LNG/30 µg EE and 7 yellow tablets containing 10 µg EE.

  • PlaceboDrug

    1 tablet daily to match experimental arm

Study groups in NCT00781456
Study groupRoleWhat they receive
91-day Levonorgestrel Oral ContraceptiveExperimentalParticipants received 12 weeks (84 consecutive days) of active combination tablets containing 150 µg levonorgestrel (LNG)/30 µg ethinyl estradiol (EE), followed by 7 days of 10 µg EE monotherapy, for a total of 13 weeks.
Receives: Drug: 91-day Levonorgestrel Oral Contraceptive
PlaceboPlacebo comparatorParticipants received placebo, 12 weeks (84 consecutive days) of inactive tablets, followed by an additional 7 days of inactive tablets, for a total of 13 weeks.
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percentage of Participants With ≥ 50% Reduction in Migraine Frequency During the Treatment Period

    The number of participants with at least 50% reduction in migraine frequency (average weekly number of migraine episodes) through the end of the 91-day treatment period compared with Baseline (the 25- to 35-day baseline qualification period). Participants recorded the incidence, timing and intensity of migraines in a migraine diary during the prequalification period and throughout the 91-day treatment period.

    Measured: Baseline (25-35 days before Day 1) and Days 1-91

Secondary outcomes (7)
  1. Percentage of Participants With ≥ 50% Reduction in Migraine Frequency During the First, Second and Third Months

    The percentage of participants with at least 50% reduction in migraine frequency (average weekly number of migraine episodes) compared to Baseline at each month of the treatment period.

    Measured: Baseline, Month1, Month 2 and Month 3

  2. Change From Baseline in Average Migraine Severity

    Migraine severity was recorded by participants in the Baseline qualification diary and study migraine diary during the treatment period. Participants could report a severity of none (score = 0), mild (1), moderate (2), or severe (3). In general, if a headache was mild, daily activities could be resumed and little to no medication was taken. Moderate headaches required medication and effected daily activities. Severe headaches were debilitating and required medication.

    Average migraine severity is defined as the sum of the severity ratings divided by the total number of migraine episodes reported during the observation period (for example, Baseline, First Month, Second Month, Third Month, and 91-Day Treatment Period). A negative change from Baseline score indicates improvement in severity.

    Measured: Baseline and Month 1, Month 2 and Month 3

  3. Percentage of Participants Who Required Rescue Medications During the Study Period

    Participants recorded use of rescue medications for migraines in the migraine diary during the course of study treatment.

    Measured: Baseline, Month 1, Month 2 and Month 3

  4. Change From Baseline in Migraine Disability Assessment

    The migraine disability assessment (MIDAS) test is used to determine how severely migraines affect a patient's life. Participants were asked five questions about how often their headaches limited their ability to go to work or school, to do household work or to do family or leisure activities in the past 3 months.

    The MIDAS score equals the sum of the days answered for each question and ranges from 0 (no disability) to approximately 270 (severe disability; the upper bound is dependent on the number of days a participant would plan to work or participate in other activities).

    The MIDAS score is classified into four grades of severity:

    • 0 to 5: MIDAS Grade I, Little or no disability
    • 6 to 10: MIDAS Grade II, Mild disability
    • 11 to 20: MIDAS Grade III, Moderate disability
    • 21+: MIDAS Grade IV, Severe disability

    Measured: Baseline and Week 15

  5. Change From Baseline in Headache Impact Test

    The Headache Impact Test (HIT) is a tool used to measure the impact headaches have on patients' ability to function on the job, at school, at home and in social situations.

    HIT-6 consists of 6 questions each scored on a scale from Never (6 points) to Always (13 points). The total score ranges from 36 to 78 with higher scores indicating greater impact on life.

    There was an error in administration of the HIT-6 in this study. Question 6 was not administered, and question 3 from the MIDAS was included instead. Therefore, the total score of the HIT-6 could not be calculated.

    Measured: Baseline and Week 15

  6. Number of Participants With Adverse Events (AEs)

    An AE is any untoward medical occurrence in a clinical investigation participant and which does not necessarily have to have a causal relationship with this treatment or clinical study.

    The following definitions were used to assess AE severity: Mild: Awareness of signs or symptoms, but they are easily tolerated; Moderate: Enough discomfort to cause interference with usual activity; Severe: Incapacitating, with inability to perform usual activity.

    Relationship to study drug was assessed as either: None: Causal relationship can be ruled out; Possibly: Causal relationship at least reasonably possible, i.e. relationship cannot be ruled out; Definitely: Causal relationship is certain.

    A serious adverse event (SAE) is one that met any one of the following criteria:

    • Fatal or life threatening
    • Requires or prolongs in patient hospitalization
    • Results in persistent or significant disability/incapacity
    • Congenital anomaly / birth defect
    • Important medical event.

    Measured: Up to 15 weeks

  7. Mean Number of Days of Bleeding or Spotting

    Bleeding and spotting were recorded by participants in the migraine diary during the 91-day treatment period.

    Measured: 91-day treatment period

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Oct 2008 (estimated)
  2. Study startJan 2009
  3. Primary completionAug 2011
  4. Study completionAug 2011

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
109 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00781456
Sponsor's protocol ID
DR-105-201
Status last verified
Dec 2016
First submitted
28 Oct 2008
Last updated
6 Feb 2017
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing 91-day Levonorgestrel Oral Contraceptive in people with Migraine, run by Duramed Research at 22 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 6 Feb 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 22 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 29 Aug 2014). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percentage of Participants With ≥ 50% Reduction in Migraine Frequency During the Treatment Period (time frame: Baseline (25-35 days before Day 1) and Days 1-91). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Feb 2017.

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