Recommendations for standardization of data collection and analysis of bleeding in combined hormone contraceptive trials

This is the second of a two-article series describing the outcomes of the Hormonal Contraceptives Trial Methodology Consensus Conference held in Philadelphia, PA, on September 23, 2005. The first manuscript, "Hormonal Contraceptive Trials: Variable Data Collection and Bleeding Assessment Methodologies Influence Study Outcome and Physician Perception," provided a description of methodologies applied in the US Food and Drug Administration medical officer's review of clinical trial data as contained in the Summary Basis of Approvals of New Drug Applications, results of the review and general conclusions. This manuscript provides recommendations regarding best practices in trial design, data collection and analysis regarding bleeding data in combined hormone contraception trials.

Contributors

Mishell, D. R., Jr. Guillebaud, J. Westhoff, C. Nelson, A. L. Kaunitz, A. M. Trussell, J. Davis, A. J.

Publication

Journal: Contraception
Volume: 75
Issue: 1
Pages: 11 - 5
Year: 2007
DOI: 10.1016/j.contraception.2006.08.012

Further Study Information

Current Stage: Not Applicable
Date:
Funding source(s): Unrestricted educational grant from Duramed Pharmaceuticals


Health Area

Disease Category: Gynaecology

Disease Name: N/A

Target Population

Age Range: Unknown

Sex: Female

Nature of Intervention: Drug

Stakeholders Involved

- Researchers

Study Type

- Recommendations for outcome measures (measurement/how)

Method(s)

- Consensus conference