Effects of Drospirenone-Containing or -Not Containing Combined Oral Contraceptives on General and Sexual Well-Being - Full Text View

Effects of Drospirenone-Containing or -Not Containing Combined Oral Contraceptives on General and Sexual Well-Being (COSME)

This study is currently recruiting participants.

Verified by Bayer, October 2009

First Received: October 1, 2009 No Changes Posted

Sponsor:	Bayer
Information provided by:	Bayer
ClinicalTrials.gov Identifier:	NCT00988910

Purpose

The purpose of this study is to evaluate the symptoms and satisfaction for women taking drospirenone (DRSP)-containing combined oral contraceptives in comparison with women taking other kind of combined oral contraceptives.

Condition	Intervention
Contraception	Drug: EE30-DRSP (Yasmin, BAY86-5131) Drug: Other combined oral contraceptives

Study Type:	Observational
Study Design:	Cohort, Prospective
Official Title:	Observational Study on the Effects of DRSP-Containing Combined Oral Contraceptives (Yasmin,Yasminelle) and Other Combined Oral Contraceptives on the General and Sexual Well-Being in COC Users

Further study details as provided by Bayer:

Primary Outcome Measures:

Psychophysical well-being evaluated by the Psychological General Well-Being Index (PGWBI) [ Time Frame: at 12 months ] [ Designated as safety issue: No ]
Sexual well-being evaluated by the Female Sexual Function Index (FSFI) [ Time Frame: at 12 months ] [ Designated as safety issue: No ]

Biospecimen Retention: None Retained

Biospecimen Description:

Estimated Enrollment:	600
Study Start Date:	January 2008
Estimated Study Completion Date:	September 2009
Estimated Primary Completion Date:	September 2009 (Final data collection date for primary outcome measure)

Groups/Cohorts	Assigned Interventions
Group 1	Drug: EE30-DRSP (Yasmin, BAY86-5131) DRSP-containing combined oral contraceptives according to the normal routine praxis
Group 2	Drug: Other combined oral contraceptives Other combined oral contraceptives according to the normal routine praxis

Eligibility

Ages Eligible for Study:	18 Years to 45 Years
Genders Eligible for Study:	Female
Accepts Healthy Volunteers:	Yes
Sampling Method:	Non-Probability Sample

Study Population

Healthy women using Combined Oral Contraceptive (COC)

Criteria

Inclusion Criteria:

According to the label of the prescribed Combined Oral Contraceptive (COC)
First Combined Oral Contraceptive use or previous Combined Oral Contraceptive use
Intention to use current COC for 1 year at least

Exclusion Criteria:

Contraindications listed in the label of the prescribed Combined Oral Contraceptive (COC)

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00988910

Contacts

Contact: Bayer Clinical Trials Contact

clinical-trials-contact@bayerhealthcare.com

Locations

Italy
	Recruiting
Many Locations, Italy

Sponsors and Collaborators

Bayer

Investigators

Study Director:

Bayer Study Director

Bayer

More Information

Additional Information:

Click here and search for drug information provided by the FDA This link exits the ClinicalTrials.gov site

Click here and search for information on any recalls, market or product safety alerts by the FDA which might have occurred with this product This link exits the ClinicalTrials.gov site

Click here to find results for studies related to marketed products This link exits the ClinicalTrials.gov site

No publications provided

Responsible Party:	Bayer HealthCare AG ( Medical Director )
Study ID Numbers:	14182, YA0711IT
Study First Received:	October 1, 2009
Last Updated:	October 1, 2009
ClinicalTrials.gov Identifier:	NCT00988910 History of Changes
Health Authority:	Italy: Ethics Committee

Keywords provided by Bayer:

Combined Oral Contraceptives
COC

Additional relevant MeSH terms:

Contraceptives, Oral, Combined
Contraceptive Agents
Therapeutic Uses
Physiological Effects of Drugs

Contraceptives, Oral
Contraceptive Agents, Female
Reproductive Control Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on February 08, 2010