A Complex Contraception Registry

NCT02219269 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 97

Last updated 2018-03-14

No results posted yet for this study

Summary

The investigators will conduct a prospective observational cohort study to investigate factors that influence contraceptive method utilization among women with medical conditions. The investigators will also investigate how women with medical conditions access to contraception and family planning fellowship trained specialist. After the baseline questionnaire, there be a 3 month and 6 month follow up questionnaire to investigate continuation and satisfaction with the contraceptive method. This study is unique because it will allow us to explore doing collaborative family planning research at the multiple UC medical campuses.

Conditions

Sponsors & Collaborators

Principal Investigators

  • Jody Steinauer, MD · University of California, San Francisco

  • Radhika Rible, MD MS · University of California, Los Angeles

  • Tabetha Harken, MD MPH · UC Irvine

  • Catherine Cansino, MD MPH · UC Davis

  • Sheila Mody, MD MPH · UCSD

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-06-30
Primary Completion
2015-06-30
Completion
2015-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02219269 on ClinicalTrials.gov