Skip to main content
MedPathMedPath Home
Clinical Trials/CTRI/2022/07/044124
CTRI/2022/07/044124
Recruiting
Phase 3

Assessment of the Effect of Pre-natal and Post-natal Maternal Behavioral Change Communication (BCC) intervention on the Dental Caries Experience of their children - BCC-DPHP

Amrita School of Dentistry0 sites0 target enrollmentTBD
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsHealth Condition 1: K026- Dental caries on smooth surfaceHealth Condition 2: O00-O9A- Pregnancy, childbirth and the puerperium

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: K026- Dental caries on smooth surfaceHealth Condition 2: O00-O9A- Pregnancy, childbirth and the puerperium
Sponsor
Amrita School of Dentistry
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Amrita School of Dentistry

Eligibility Criteria

Inclusion Criteria

  • •1\. Nulliparous pregnant women aged 20\-35 years.
  • •2\. Non cavitated or restorable dental carious lesions \[ICDAS 1\-5] of DMFT \= 3, consenting to fulfil all their dental needs at the prescribed study interval.
  • •3\. Understands the importance of dental caries prevention and accepts preventive dental measures as beneficial for themselves and their children.
  • •4\. Absence of any relevant systemic medical condition.
  • •5\. Consent to comply with all the trial requirements.

Exclusion Criteria

  • •1\. High risk and multiple pregnancies
  • •2\. Developmental dental abnormalities or grossly destructed teeth that may be difficult to restore or undergo surgical removal during the trial period.
  • •3\. With known cognitive and psychological impairment.
  • •4\. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial.
  • •5\. Participants who have participated in any similar research trial in the past 12 weeks.

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Phase 3
Comparison study on the effect of prenatal administation of high dose and low dose folic acid on surem RANKL/OPG ratio in pregnancypregnant women.Eclampsia
IRCT2013122315903N1Drug Applied Research Center, Tabriz University of Medical Sciences- Tabriz- iran88
Active, not recruiting
Phase 1
Enalapril to improve heart function following preterm pre-eclampsia.
EUCTR2017-003180-35-GBManchester University NHS Foundation Trust80
Not yet recruiting
Phase 3
Assessment of Perinatal Outcome after Sustained Tocolysis in Early Labour (APOSTEL II)threatened preterm labour10010273
NL-OMON30860Academisch Medisch Centrum400
Recruiting
Not Applicable
Effect of Premature Infant Oral Motor Intervention in neonatal outcomes; Effect of Maternal stress in outcomes in neonatal outcomes
IRCT20220124053823N1Arak University of Medical Sciences62
Recruiting
Not Applicable
DIPLOMATICPregnancy and Childbirth
PACTR202010788566263niversity of Edinburgh ACCORD office12,000