Clinical Trials Directory

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UnknownNCT01590849

Assessment of Autonomic Tone in Normotensive Women Using Combined Hormonal Oral Contraceptive Containing Drospirenone

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
69 (actual)
Sponsor
Instituto do Coracao · Other Government
Sex
Female
Age
20 Years – 40 Years
Healthy volunteers
Accepted

Summary

The use of combined oral contraceptives has been associated with increased risk of adverse cardiovascular events. The exact mechanism by which these drugs exert this influence is uncertain. It is possible that changes in autonomic nervous system are involved. The objective of these study was to evaluate the effect of the use of a contraceptive containing 20 mcg of ethinyl estradiol and 3mg of drospirenone in the autonomic nervous system in healthy women. Few studies have been conducted in the field of hormonal contraception and evaluation of the autonomic nervous system work and no prospective, controlled study was published so far. These study will be the first.

Conditions

Interventions

TypeNameDescription
DRUGContraceptives, Oral, Combined (Yaz®)After a counseling session concerning the advantages, disadvantages and side effects of contraceptive methods (COC or nonhormonal methods), the volunteers were divided into two study groups according to the method they chose to use as follows: * Case group: healthy women, users of COC containing 20 mcg ethynil estradiol and 3 mg drospirenone , 24 days of active pills, 4 days of pill-free interval (n=40). * Control group: healthy women, users of nonhormonal methods of contraception (condoms or copper IUD) (n=40). Subjects were tested once before the introduction of the contraceptive method and again after 6 months of its use.

Timeline

Start date
2011-01-01
Primary completion
2012-05-01
First posted
2012-05-03
Last updated
2012-05-03

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01590849. Inclusion in this directory is not an endorsement.