Clinical Trials Directory

Trials / Completed

CompletedNCT01650168

Prospective Controlled Cohort Study on the Safety of a Monophasic Oral Contraceptive Containing Nomegestrol Acetate (2.5mg) and 17ß-estradiol (1.5mg)

Status
Completed
Phase
Study type
Observational
Enrollment
101,498 (actual)
Sponsor
Center for Epidemiology and Health Research, Germany · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

Summary

This study compares the risks of short- and long-term use of NOMAC-E2 (containing a fixed dose of nomegestrol acetate and estradiol) compared with levonorgestrel-containing combined oral contraceptives (COC-LNG) in a study population representative of the actual users of the individual preparations.

Detailed description

NOMAC-E2 is a novel monophasic oral contraceptive containing a fixed dose of nomegestrol acetate (2.5mg) and 17ß-estradiol (1.5mg) which is taken for 24 days followed by 4 days of placebo. The most relevant adverse clinical outcome that has been linked to the use of COCs is venous thromboembolism (VTE). Data from randomized clinical trials did not show any serious health concerns for NOMAC-E2. However, the statistical power to detect rare adverse events is limited in these studies. PRO-E2 is a large, prospective, controlled, long-term active surveillance study to investigate the safety of NOMAC-E2 with regard to the outcomes of interest. This study follows the European Active Surveillance (EURAS) design methodology with some modifications due to country- and product-specific characteristics. The outcomes of interest will be validated via the attending physicians. A multi-faceted follow-up procedure will ensure a low loss to follow-up rate. This study will involve women from Europe and Australia who will be followed for up to 2 years. Data analysis will include multivariable techniques such as Cox regression.

Conditions

Timeline

Start date
2012-07-01
Primary completion
2020-12-01
Completion
2020-12-01
First posted
2012-07-26
Last updated
2021-07-28

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01650168. Inclusion in this directory is not an endorsement.