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.
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
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 group | Role | What they receive |
|---|---|---|
| 91-day Levonorgestrel Oral Contraceptive | Experimental | Participants 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 |
| Placebo | Placebo comparator | Participants 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.
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)
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
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
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
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
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
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
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.
- First posted29 Oct 2008 (estimated)
- Study startJan 2009
- Primary completionAug 2011
- Study completionAug 2011
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for MigraineStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Duramed Research
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Duramed Research Protocol Chair, Study chair, Duramed Research, Inc.
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
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Feb 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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.
- ClinicalTrials.gov ID
- NCT00781456
- Acronym / sponsor ID
- DR-105-201
- Conditions
- Migraine
- Keywords
- Migraine headache, menstrual, oral contraceptive, Menstrually-Related Migraine Headache
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 109 participants (actual)
- Lead sponsor
- Duramed ResearchIndustry (pharma, biotech, devices)
- Study start
- Jan 2009
- Primary completion
- Aug 2011 (actual)
- Study completion
- Aug 2011 (actual)
- First posted
- 29 Oct 2008 (estimated)
- Results
- Posted 29 Aug 2014
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 91-day Levonorgestrel Oral Contraceptive | Experimental | Drug: 91-day Levonorgestrel Oral ContraceptiveParticipants 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. |
| Placebo | Placebo comparator | Drug: PlaceboParticipants 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. |
Who may qualify
- Ages
- 18 to 34 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- 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
Key exclusion criteria (3 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| 91-day Levonorgestrel Oral ContraceptiveAlso: Seasonique, DR-10591-day treatment consisting of 84 blue combination tablets containing 150 µg LNG/30 µg EE and 7 yellow tablets containing 10 µg EE. | Drug | 91-day Levonorgestrel Oral Contraceptive |
| Placebo1 tablet daily to match experimental arm | Drug | Placebo |
Primary outcome
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
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.
7 secondary outcomes
Percentage of Participants With ≥ 50% Reduction in Migraine Frequency During the First, Second and Third Months
Time frame: Baseline, Month1, Month 2 and Month 3
Change From Baseline in Average Migraine Severity
Time frame: Baseline and Month 1, Month 2 and Month 3
Percentage of Participants Who Required Rescue Medications During the Study Period
Time frame: Baseline, Month 1, Month 2 and Month 3
Change From Baseline in Migraine Disability Assessment
Time frame: Baseline and Week 15
Change From Baseline in Headache Impact Test
Time frame: Baseline and Week 15
Number of Participants With Adverse Events (AEs)
Time frame: Up to 15 weeks
Mean Number of Days of Bleeding or Spotting
Time frame: 91-day treatment period
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Feb 2017.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Duramed Research Protocol Chair study chair
Duramed Research, Inc.
22 sites in 1 country: see every site and its status.
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.