Human Papillomavirus (HPV) Infection in Pregnancy

The recruitment status of this study is unknown because the information has not been verified recently.

Verified June 2007 by University of Pennsylvania.
Recruitment status was Recruiting

Sponsor:

Collaborator:

National Institutes of Health (NIH)

Information provided by:

University of Pennsylvania

ClinicalTrials.gov Identifier:

NCT00194311

First received: September 13, 2005

Last updated: June 20, 2007

Last verified: June 2007

History of Changes

Tracking Information

First Received Date ^ICMJE

September 13, 2005

Last Updated Date

June 20, 2007

Start Date ^ICMJE

April 2005

Primary Completion Date

Not Provided

Current Primary Outcome Measures ^ICMJE

Not Provided

Original Primary Outcome Measures ^ICMJE

Not Provided

Change History

Complete list of historical versions of study NCT00194311 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^ICMJE

Not Provided

Original Secondary Outcome Measures ^ICMJE

Not Provided

Current Other Outcome Measures ^ICMJE

Not Provided

Original Other Outcome Measures ^ICMJE

Not Provided

Descriptive Information

Brief Title ^ICMJE

Human Papillomavirus (HPV) Infection in Pregnancy

Official Title ^ICMJE

Not Provided

Brief 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.

Detailed Description

Not Provided

Study Type ^ICMJE

Observational

Study Design ^ICMJE

Observational Model: Case Control
Time Perspective: Cross-Sectional
Time Perspective: Prospective

Target Follow-Up Duration

Not Provided

Biospecimen

Not Provided

Sampling Method

Not Provided

Study Population

Not Provided

Condition ^ICMJE

Papillomavirus Infections
Pregnancy Complications

Intervention ^ICMJE

Not Provided

Study Group/Cohort (s)

Not Provided

Publications *

Not Provided

* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Recruiting

Estimated Enrollment ^ICMJE

620

Completion Date

Not Provided

Primary Completion Date

Not Provided

Eligibility Criteria ^ICMJE

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

Gender

Female

Ages

13 Years to 45 Years

Accepts Healthy Volunteers

Yes

Contacts ^ICMJE

Contact: Juan Gonzalez, MD

215 662 6913

jugonzalez@obgyn.upenn.edu

Location Countries ^ICMJE

United States

Administrative Information

NCT Number ^ICMJE

NCT00194311

Other Study ID Numbers ^ICMJE

801452, R01 HD42100-15

Has Data Monitoring Committee

Not Provided

Responsible Party

Not Provided

Study Sponsor ^ICMJE

University of Pennsylvania

Collaborators ^ICMJE

National Institutes of Health (NIH)

Investigators ^ICMJE

Principal Investigator:

Samuel Parry, MD

University of Pennsylvania

Information Provided By

University of Pennsylvania

Verification Date

June 2007

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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