Risk Factors of Ectopic Pregnancy
Completed
Conditions studied: Ectopic Pregnancy
In brief
The purpose of this study is to identify elements of a patient's demographics, history, and clinical presentation that may aid in differentiating between patients with an ectopic pregnancy, miscarriage, or normal intrauterine pregnancy. This study will also evaluate serial levels of human chorionic gonadotropin in the serum of these patients, as another way to make the diagnosis.
Key facts
- Study ID
- NCT00194207
- Run by
- University of Pennsylvania
- People needed
- 3000
- Starts
- 1999-10-01
- Expected to finish
- 2007-01-01
- Last updated by the study team
- 2016-08-17
Who can join
Age: any. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Reproductive-aged women
- Currently pregnant based on serum human chorionic gonadotropin test
- Present for care for vaginal bleeding and/or pelvic pain
- Final diagnosis of:
- Ectopic pregnancy
- Miscarriage less than 14 weeks gestation
- Ongoing normal intrauterine pregnancy less than 14 weeks gestation
- Entered into clinical tracking database
You may not qualify if…
- Patients not entered in clinical tracking database, or with insufficient information recorded to analyze (e.g. missing final diagnosis)
Where it is running
- University of Pennsylvania Reproductive Research Unit — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.