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Clinical Trials/CTRI/2024/05/067871
CTRI/2024/05/067871
Not yet recruiting
Phase 4

Comparative evaluation of clinical and radiographic outcomes of indirect pulp capping using protooth cement and biodentine in carious primary molars- An in-vivo study. - NI

Dr N Devi Vyshnavi0 sites0 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: K040- Pulpitis
Sponsor
Dr N Devi Vyshnavi
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Dr N Devi Vyshnavi

Eligibility Criteria

Inclusion Criteria

  • 1\)The primary molars with no spontaneous pain, no tenderness to percussion or palpation
  • 2\)Primary molars with a deep carious lesion approximating pulp.
  • 3\)Presence of active carious lesions involving occlusal surfaces of primary molars.
  • 4\)Extension of carious lesion such that complete caries removal would risk pulp exposure.
  • 5\)Cooperative children and parents willing to follow the instructions and report for follow\-up.
  • Radiographic:
  • 1\)No radiographic signs of internal or external root resorption
  • 2\)Radiographic evidence of an intact lamina dura.
  • 3\)Dental caries close to the pulp.

Exclusion Criteria

  • 1\)Patients who decline to participate in the study.
  • 2\)History of spontaneous sharp, penetrating pain, or tenderness on percussion.
  • 3\)Presence of abnormal tooth mobility, fistula, abscess, and swelling of the soft and periodontal tissues.
  • 4\)Presence of chronic systemic diseases.
  • Radiographic:
  • 1\)Large carious lesion with radiographic pulp exposure.
  • 2\)Presence of interrupted lamina dura, internal or external root resorption, interradicular or periapical pathosis, and widened periodontal ligament space

Outcomes

Primary Outcomes

Not specified

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