Periodontal Infection and Prematurity Study
This study is currently recruiting patients
Verified by University of Pennsylvania September 2006
| Sponsored by: |
University of Pennsylvania |
| Information provided by: |
University of Pennsylvania |
| ClinicalTrials.gov Identifier: |
NCT00116974 |
Purpose
This research project is a multi-center double-blind, parallel, randomized, controlled clinical trial design comparing the efficacy of dental scaling and root planing to control treatment (superficial cleaning) for the prevention of preterm birth in pregnant women with periodontal disease.
| Condition |
Intervention |
Phase |
Periodontal Diseases Premature Birth
|
Procedure: Scaling and root planing
|
Phase III
|
Study Type: Interventional Study Design: Prevention, Randomized, Double-Blind, Active Control, Parallel Assignment
Eligibility
Genders Eligible for Study:
Female
Criteria
Inclusion Criteria:
- Gestational age between 6 and 20 completed weeks
Exclusion Criteria:
- Periodontal treatment during the pregnancy
- Antibiotic use within 2 weeks of enrollment
- Use of antimicrobial mouthwash within 2 weeks
- Multiple gestation
- Known mitral valve prolapse
Location
and Contact
Information
Please refer to this study by ClinicalTrials.gov identifier
NCT00116974
Pennsylvania Hospital of the University of Pennsylvania, Philadelphia,
Pennsylvania,
19104,
United States; Recruiting
Bonnie A. Clothier, MSN, CRNP
215-662-6360
bclothier@obgyn.upenn.edu
George A. Macones, MD, MSCE, Principal Investigator
Study chairs or principal investigators
George A Macones, M.D., Principal Investigator, University of Pennsylvania
More Information
Study ID Numbers:
801404
Last Updated:
September 7, 2006
Record first received:
June 30, 2005
ClinicalTrials.gov Identifier:
NCT00116974Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2006-09-29
|