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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT02257671 |
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Date of registration:
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28/09/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Oral Contraceptives and Economic Behaviour
P-piller101 |
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Scientific title:
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The Influence of Oral Contraceptives on Mood, Sexuality and Economic Behavior |
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Date of first enrolment:
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February 2012 |
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Target sample size:
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400 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT02257671 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Sweden
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Contacts
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Name:
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Angelica L Hirschberg, Professor |
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Address:
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Telephone:
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+46 8 517 733 26 |
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Email:
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angelica.linden-hirschberg@karolinska.se |
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Affiliation:
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Name:
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Angelica L Hirschberg, Professor |
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Address:
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Telephone:
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+46 8 517 733 26 |
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Email:
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angelica.linden-hirschberg@karolinska.se |
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Affiliation:
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Name:
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Angelica L Hirschberg, Professor |
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Address:
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Telephone:
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Email:
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Affiliation:
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Department of Obstetrics and Gynecology, Karolinska University Hospital, Stockholm, Sweden |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Healthy young women, aged 18-35 years, BMI 19-30
Exclusion Criteria:
- Risk factors for thrombosis, smoking, obesity, hypertension, diabetes and
estrogen/gestagen therapy the last three months
Age minimum:
18 Years
Age maximum:
35 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Female Contraception
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Intervention(s)
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Drug: Oral contraceptive
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Primary Outcome(s)
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sexual behaviour
[Time Frame: baseline to 11 weeks]
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economic behaviour
[Time Frame: 11 weeks]
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mood
[Time Frame: baseline to 11 weeks]
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Secondary ID(s)
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2010-020824-23
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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