Effect of maternal oral health on new borns in pregnant patients.

Effect of Early Periodontal Therapy on Pregnancy Outcomes- A Randomized Control Trial. - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/062066

Enrollment

800

Registered

2024-01-30

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O269- Pregnancy related conditions, unspecified

Interventions

Intervention1: Early Periodontal Therapy: Pregnant females would be given CPHC in the form of structured early periodontal therapy ( 10 weeks of gestation) . This includes Oral prophylaxis in the form

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with confirmed pregnancy through UPT or through USG. 2. All pregnant female in age range of 18 to 35 years with a BMI of 18.5 to 24.9 with at least 20 teeth as a part of dentition would be included in the study.

Exclusion criteria

Exclusion criteria: a. History of Frequent diagnosed UTI in preconception period ( >3 episodes/year). b. Diagnosed preconception chronic disease conditions like uncontrolled Diabetes, Hypertension, Thyroid Diseases, AIDS, and Chronic Liver and Renal diseases. c. History of unexplained Preterm Labour, Preeclampsia, or stillbirth. d. History of Diagnosed Autoimmune diseases (SLE, Rheumatoid Arthritis, Sjogren Syndrome, Ulcerative Colitis, Antiphospholipid Syndrome.) e. Previous surgeries on the cervix. f. Multifetal Gestation. g. Contraindication to periodontal probing such as Congestive cardiac disease. h. Medications that result in gingival overgrowth such as phenytoin, cyclosporin, and calcium channel blockers.

Design outcomes

Primary

Measure	Time frame
The following outcome would be measured in both the groups: 1.Proportion of preterm births.Timepoint: Every 1-2 Months coinciding with ANC	—

Secondary

Measure	Time frame
The following outcomes would be measured in both the groups: 1. Mean birth weight of neonates. 2. Proportion of new born with Low birth weight. 3. Proportion of preeclampsia in pregnant female. 4. Proportion of IUGR seen during pregnancy 5. Periodontal health of the mother. 6. Any adverse outcomes Timepoint: Every 1-2 Months coinciding with ANC	—

Countries

India

Contacts

Public ContactDrKirti Chaudhry

AIIMS Jodhpur

chaudhry_kirti@yahoo.com08003993889

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026