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COMPARISON of MINERAL TRIOXIDE AGGREGATE and CALCIUM HYDROXIDE AS INDIRECT PULP CAPPING AGENTS in PRIMARY MOLARS

S

Shaheed Zulfiqar Ali Bhutto Medical University

Status and phase

Completed
Phase 4

Conditions

Indirect Pulp Cap

Treatments

Drug: MTA pulp dressing material
Drug: Calcium Hydroxide (Ca(OH)2)

Study type

Interventional

Funder types

Other

Identifiers

NCT06807320
F.1-1/2015/ERB/SZABMU/ERB

Details and patient eligibility

About

The study is designed as randomized clinical trial performed at the Department of Pediatric Dentistry , Pakistan Institute of Medical Sciences (PIMS) , Islamabad on primary molars requiring indirect pulp treatment in patients aged 5 to 9 years. Two groups , I and II of 40 teeth each will be selected according to inclusion criteria . In Group I , indirect pulp capping will be done with Calcium hydroxide while in Group II , it will be done with MTA . Both the groups will be evaluated clinically and radiographically at 0, 3 and 6 months . Results were compiled and analyzed using standard statistical techniques.

Enrollment

40 patients

Sex

All

Ages

4 to 8 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Clinical Criteria :

    • Primary molars with deep carious lesions
    • No H/O spontaneous pain
    • No associated swelling
    • No tenderness to percussion
    • Absence of pathological mobility
    • No sinus tract
    • Restorable

Radiographic Criteria :

  • No periapical radiolucency
  • No loss of lamina dura
  • No physiological root resorption
  • Teeth with radiographic evidence of more than 0.25mm remaining dentin thickness
  • No furcal radiolucency

Exclusion criteria

  • Non restorable teeth

    • Teeth with pathological mobility
    • Teeth with extensive external/internal root resorption.
    • Teeth with pulp canal calcifications
    • Subjects inability to tolerate any of the dental products being used
    • Systemic disease or severe medical complications ; Lack of compliance

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Single Blind

40 participants in 2 patient groups

Group I patients, Calcium hydroxide
Active Comparator group
Description:
For Group I patients, Calcium hydroxide (Dycal_ Ivory,Dentsply Caulk, Dentsply, L.D. Caulk, Milford, DE,USA ) was used. The catalyst and paste were mixed as per the manufacturer's recommendations.
Treatment:
Drug: Calcium Hydroxide (Ca(OH)2)
Group II patients, MTA
Experimental group
Description:
MTA powder ( ProRoot; Dentsply ⁄ Tulsa Dental, Tulsa, OK,USA) was added to sterile water. The mixture was left to achieve a sandy consistency for about thirty seconds. Then, the material was applied to the cavity using a ball condenser.
Treatment:
Drug: MTA pulp dressing material

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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