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Clinical Trials/NCT07333872
NCT07333872Active, not recruitingNot Applicable

Evaluation of Pulpotomy, Partial Pulpotomy, and Direct Pulp Capping Using Mineral Trioxide Aggregate in Primary Molars. A Randomized Clinical Trial.

Delta University for Science and Technology1 site in 1 country96 target enrollmentStarted: June 1, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
96
Locations
1
Primary Endpoint
Spontaneous pain

Study Overview

Brief Summary

A comparative evaluation for three vital pulp therapy techniques in primary molars using the same material (MTA)

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
4 Years to 7 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • articipants were cooperative children (4-7 years) with no systemic diseases or relevant allergies. Eligible teeth were restorable primary second molars with deep carious lesions and a diagnosis of reversible pulpitis,

Exclusion Criteria

  • spontaneous pain, edema, fistula, pathological mobility, or percussion sensitivity.

Outcomes

Primary Outcomes

Spontaneous pain

Time Frame: 12 months

numeric rating scale (presence or abscence of pain) 0 is best result 10 is the worst

Radiolucency of the periapical or furcation area

Time Frame: Follow up for 12 months

measuring tool is x-ray

Spontaneous pain

Time Frame: 12 months

numeric rating scale (presence or abscence of pain) 0 is best result 10 is the worst

Radiolucency of the periapical or furcation area

Time Frame: Follow up for 12 months

measuring tool is x-ray

Secondary Outcomes

  • Presence or absence of fistula(12 months)
  • Pathological mobility(12 months)
  • Sensitivity on percussion(12 months)
  • Widening of personal ligament space(12 months)
  • Pathological mobility(12 months)
  • Presence or absence of fistula(12 months)
  • Sensitivity on percussion(12 months)
  • Widening of personal ligament space(12 months)
  • Internal or e ternal resorption(12 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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