A Complex Contraception Registry

Completed

Conditions studied: Diabetes, Cardiovascular Disease, Epilepsy, Migraine, Neurological Disorders, Cancer, Bariatric Surgery Candidate, Organ or Tissue Transplant; Complications, Lupus Erythematosus, Systemic, Other Hematologic Conditions, Other Venous Embolism and Thrombosis

In brief

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.

Key facts

Study ID

NCT02219269

Run by

University of California, San Diego

People needed

97

Starts

2014-06-01

Expected to finish

2015-06-01

Last updated by the study team

2018-03-14

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Ethnic Background: No limitation, will include minorities
• Sexually Active with men
• Diagnosis with at least one of the following conditions
• Diabetes and other endocrine disorders
• Cardiovascular Disease, such as Ischemic Heart Disease, Valvular disease, hypertension or pulmonary hypertension
• Epilepsy, Migraine, and other neurologic disorders
• History of or current cancer
• History of or planning Bariatric Surgery
• History of or planning Solid Organ Transplant
• Systematic Lupus Erythematous and other rheumatologic conditions
• History of or current Venous Thrombosis Embolism
• Other Medical Conditions (such as Sickle Cell Disease or Cystic Fibrosis)

You may not qualify if…

• Pregnant at time of recruitment
• History of hysterectomy, bilateral oophorectomy, or sterilization procedure
• Unable to provide informed consent
• Attempting to become pregnant at time of recruitment
• Not sexually active with men
• No active telephone number or email for follow up
• Women who are pregnant will be excluded from this study. However, no pregnancy testing will be conducted; pregnancy status will be based on self-reporting by subjects.

Where it is running

• UCLA — Los Angeles, California, United States
• UC Irvine — Orange, California, United States
• UC Davis — Sacramento, California, United States
• UCSD — San Diego, California, United States
• UCSF — San Francisco, California, United States

Full record on ClinicalTrials.gov

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