The Effects of Pregnancy on Oral Health

NCT06343337 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 198

Last updated 2024-04-02

No results posted yet for this study

Summary

The aim of this study was to evaluate the effects of pregnancy on salivary pH, flow rate, caries experience and periodontal status.

The main questions it aims to answer are:

* Does pregnancy affect caries experience and periodontal status?
* Does pregnancy affect salivary pH and flow rate?
* Is there a difference between pregnant and non-pregnant woman with respect to caries experience, periodontal status, salivary pH and flow rate?
* Is there a difference among first, second and third trimester with respect to caries experience, periodontal status, salivary pH and flow rate?

Conditions

  • Pregnancy Related
  • Dental Caries
  • Periodontal Diseases
  • Saliva Altered

Interventions

DIAGNOSTIC_TEST

Evaluation of DMFT index, CPI scores, salivary pH and flow rate in pregnant and non-pregnant woman

Total 198 volunteer (51 women for control, 47 women for 1st trimester, 51 women for 2nd trimester, and 49 women for 3rd trimester) were included. The data about sociodemographic characteristics, dental and systemic health conditions were recorded. Unsitumulated saliva samples were collected for 5 minutes by spitting method. The pH of saliva was measured by a portable pHmeter. The salivary flow rate was determined by the weight measurement method. DMFT index and CPI scores were determined. The statistical differences were evaluated by Kruskal-Wallis, Mann Whitney U and Chi Square tests (α=.05).

Sponsors & Collaborators

  • Muğla Sıtkı Koçman University

    lead OTHER

Principal Investigators

  • FATMA YILMAZ, Asistant Professor · Muğla Sıtkı Koçman Universty

  • Ozgul Carti Dorterler, Asistant Professor · Muğla Sıtkı Koçman Universty

  • Saniye Eren Halici, Asistant Professor · Muğla Sıtkı Koçman Universty

  • Burcu Kasap, Professor · Muğla Sıtkı Koçman Universty

  • Aysegul Demirbas, Professor · Ege Universty

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-05-20
Primary Completion
2023-04-01
Completion
2023-04-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06343337 on ClinicalTrials.gov