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NCT00194311 Clinical Trial

Human Papillomavirus (HPV) Infection in Pregnancy

Pregnancy Complications Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00194311
Other study ID # 801452
Secondary ID R01 HD42100-15
Status Completed
Phase N/A
First received September 13, 2005
Last updated August 15, 2016
Start date April 2005
Est. completion date August 2007

Study information
Verified date August 2016
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine if maternal infection with human papillomavirus (HPV) is associated with pregnancy complications including spontaneous preterm delivery (sPTD), severe preeclampsia (PE), and poor fetal growth.

Recruitment information / eligibility
Status Completed
Enrollment 620
Est. completion date August 2007
Est. primary completion date August 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 13 Years to 45 Years
Eligibility Inclusion Criteria:

- All women presenting for prenatal care at the Hospital of the University of Pennsylvania or affiliated clinics

Exclusion Criteria:

- Multiple gestations

- Medical conditions such as diabetes, chronic hypertension, renal disease

- Fetal malformations or chromosomal anomalies

- Fetal death

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Hospital of the University of Pennsylvania Philadelphia Pennsylvania

Sponsors (2)
Lead Sponsor Collaborator
University of Pennsylvania National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

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