Periodontal Infection and Prematurity Study
Phase 3
Terminated
- Conditions
- Periodontal DiseasesPremature Birth
- Interventions
- Procedure: Scaling and root planing
- Registration Number
- NCT00116974
- Lead Sponsor
- University of Pennsylvania
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- Female
- Target Recruitment
- 2100
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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 1 Scaling and root planing - 2 Scaling and root planing -
- Primary Outcome Measures
Name Time Method Whether screening and treating periodontal disease using scaling and root planing early in pregnancy can reduce the incidence of spontaneous preterm birth <35 weeks 9 months
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Hospital of the University of Pennsylvania
🇺🇸Philadelphia, Pennsylvania, United States