Evaluation of Pulpotomy, Partial Pulpotomy, and Direct Pulp Capping Using Mineral Trioxide Aggregate.
1 other identifier
interventional
96
1 country
1
Brief Summary
A comparative evaluation for three vital pulp therapy techniques in primary molars using the same material (MTA)
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jun 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2025
CompletedFirst Submitted
Initial submission to the registry
January 1, 2026
CompletedFirst Posted
Study publicly available on registry
January 12, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 20, 2026
January 13, 2026
May 1, 2025
12 months
January 1, 2026
January 11, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Spontaneous pain
numeric rating scale (presence or abscence of pain) 0 is best result 10 is the worst
12 months
Radiolucency of the periapical or furcation area
measuring tool is x-ray
Follow up for 12 months
Secondary Outcomes (5)
Presence or absence of fistula
12 months
Pathological mobility
12 months
Sensitivity on percussion
12 months
Widening of personal ligament space
12 months
Internal or e ternal resorption
12 months
Study Arms (3)
Direct pulp capping
EXPERIMENTALTechnique of vital pulp therapy to cap pin point exposure
Partial pulpotomy
EXPERIMENTALTechnique of vital pulp therapy to cap widened pulp exposure
Pulpotomy
EXPERIMENTALTechnique of vital pulp therapy of capping radicular pulp after removal of coronal pulp
Interventions
Capping of the pulp tissue with a biocompatible material (MTA)
Eligibility Criteria
You may qualify if:
- 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,
You may not qualify if:
- spontaneous pain, edema, fistula, pathological mobility, or percussion sensitivity.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Delta university for science and technology
Gamasa, Dakahlia Governorate, 35516, Egypt
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 1, 2026
First Posted
January 12, 2026
Study Start
June 1, 2025
Primary Completion (Estimated)
May 31, 2026
Study Completion (Estimated)
June 20, 2026
Last Updated
January 13, 2026
Record last verified: 2025-05