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Clinical Trials/CTRI/2024/03/064694
CTRI/2024/03/064694
Not yet recruiting
Phase 3

Comparative evaluation of Platelet rich fibrin, Propolis and Mineral trioxide aggregate as pulpotomy agents in primary molars: A Randomized controlled trial - NI

mesh Kendre0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: K040- Pulpitis

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: K040- Pulpitis
Sponsor
mesh Kendre
Status
Not yet 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
mesh Kendre

Eligibility Criteria

Inclusion Criteria

  • •1\.Healthy patient between the age of 4\-9 years of age
  • •2\.Exposure of vital pulp due to dental caries, approximating to the
  • •pulp radiographically.
  • •3\.Teeth should be restorable after completion of the procedure.
  • •4\.At least two\-third of remaining root length.

Exclusion Criteria

  • •1\.Patient with draining sinus.
  • •2\.Pathological mobility.
  • •3\.History of unprovoked tooth ache or persistent tooth ache.
  • •4\.Highly viscous, sluggish, absent haemorrhage observed at radicular.
  • •5\.Periapical radiolucency.
  • •6\.Dystrophic calcification.
  • •7\.Interradicular bone loss.
  • •8\.Exfoliating tooth.
  • •9\.Presence of symptoms indicative of advanced pulpal inflammation, such as spontaneous pain or history of nocturnal pain

Outcomes

Primary Outcomes

Not specified

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