Psychosocial and Physiological Mechanisms in the Effect of Hormonal Contraception on the Female Sexual Desire
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|ClinicalTrials.gov Identifier: NCT00374387|
Recruitment Status : Completed
First Posted : September 11, 2006
Last Update Posted : March 31, 2011
75 heterosexual women are asked to use 3 different types of contraception (Nuvaring, low-dose combination pill, minipill), each during 3 months. On a monthly basis, questionnaires are filled out about sexual desire and psychosocial, relational en sexual parameters. Also the sexual desire of the partner is questioned. On a three-monthly basis, blood samples are drawn to determine changes in hormonal parameters (one sample per product period).
75 lesbian women are doing the same trial, but during an extra 3 months period, they are asked to have their natural menstrual cyclus as a control condition. Blood samples during these extra months will be drawn at the third or fourth day after start of the menses.
|Condition or disease||Intervention/treatment||Phase|
|Healthy||Drug: Nuvaring Drug: low-dose combination pill Drug: minipill||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||150 participants|
|Intervention Model:||Crossover Assignment|
|Masking:||None (Open Label)|
|Official Title:||Psychosocial and Physiological Mechanisms in the Effect of Hormonal Contraception on the Female Sexual Desire|
|Study Start Date :||September 2006|
|Actual Primary Completion Date :||August 2009|
|Actual Study Completion Date :||March 2011|
- Parameters about sexual desire and psychosocial, relational en sexual parameters.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00374387
|University Hospital Ghent|
|Ghent, Belgium, 9000|
|Principal Investigator:||Petra De Sutter, MD, PhD||University Hospital, Ghent|