Maternal Periodontal Inflammation and Pregnancy Outcomes: Salivary and Amniotic Biomarkers

Starting soon

Conditions studied: Periodontal Disease, Pregnancy, Preterm Birth

In brief

Periodontal disease is a chronic inflammatory condition that affects the tissues supporting the teeth and may contribute to systemic inflammation and oxidative stress. Increasing evidence suggests that maternal inflammation during pregnancy may be associated with adverse pregnancy outcomes, including preterm birth. However, the biological mechanisms linking maternal periodontal inflammation to the intrauterine environment remain unclear. This prospective observational cohort study aims to investigate the relationship between maternal periodontal status and inflammatory and oxidative stress biomarkers measured in both saliva and amniotic fluid. Eighty healthy pregnant women between 28 and 32 weeks of gestation will be recruited from the Obstetrics and Gynecology Clinic of Gulhane Training and Research Hospital. Participants will undergo a comprehensive periodontal examination and provide unstimulated saliva samples. Amniotic fluid samples will be collected during delivery as part of routine obstetric care, without any additional invasive procedures. The concentrations of 8-hydroxy-2'-deoxyguanosine (8-OHdG), malondialdehyde (MDA), interleukin-6 (IL-6), and matrix metalloproteinase-8 (MMP-8) will be measured in saliva and amniotic fluid using enzyme-linked immunosorbent assay (ELISA). Pregnancy outcomes, including gestational age at delivery, birth weight, and pregnancy complications, will also be recorded. The study will evaluate whether maternal periodontal inflammation is associated with changes in inflammatory and oxidative stress biomarkers in saliva and amniotic fluid and whether these biomarkers are related to pregnancy outcomes. The findings may improve understanding of the biological relationship between oral health and pregnancy and may contribute to the identification of biomarkers associated with adverse pregnancy outcomes.

Key facts

Study ID: NCT07699978
Run by: Saglik Bilimleri Universitesi
People needed: 80
Starts: 2026-08-20
Expected to finish: 2027-08-15
Last updated by the study team: 2026-07-29

Who can join

Age: 18 and older, up to 40. Sex: female. Healthy volunteers: accepted.

You may qualify if…

Pregnant women between 28 and 32 weeks of gestation
Age 18 to 40 years
Singleton pregnancy
Systemically healthy
Normal gestational diabetes screening (oral glucose tolerance test within the hospital reference range)
Receiving only routine prenatal vitamin and iron supplementation (no therapeutic medications)
Low-risk pregnancy
No history of chorioamnionitis
No periodontal treatment within the previous 6 months
Able and willing to provide written informed consent

You may not qualify if…

Multiple pregnancy
Use of antibiotics or anti-inflammatory medications during pregnancy
Current smoking or alcohol consumption
Presence of an acute infection
Placental pathology
Major fetal anomaly
High-risk pregnancy as determined by the obstetrician
Refusal or inability to provide informed consent

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.