Status:
NOT_YET_RECRUITING
Biodentine Pulpotomy vs Metapex Pulpectomy in Primary Molars: Clinical & Radiographic Comparison of Outcomes in Irreversible Pulpitis Cases
Lead Sponsor:
Mohamed Ahmed Hamdi Abo El Yamin
Conditions:
Dental Caries
Eligibility:
All Genders
4-9 years
Phase:
NA
Brief Summary
Irreversible pulpitis is defined as a clinical diagnostic based on subjective and objective findings suggesting that the vital inflamed pulp is incapable of healing in the American Association of Endo...
Detailed Description
Pulp interventions combine a medication with a pulp treatment technique. Preserving the health of the tooth and its supporting tissues is the aim of these procedures. Three pulp therapy options are av...
Eligibility Criteria
Inclusion
- • Patient and parent showing cooperation and compliance.
- Children 4-9 years old
- Vital deeply carious primary(s) with complete root formation
- Asymptomatic teeth or without clinical symptoms of spontaneous pain
- No clinical evidence of pulp degeneration like the history of spontaneous or nocturnal pain, tenderness to percussion, pathologic tooth mobility, swelling, or fistulous tract.
- Both genders will be included.
- No radiographic evidence of pulp degeneration such as internal root resorption, external root resorption, or furcal radiolucency.
- Presence of 2/3rd of root
- Teeth that can be restored
- Children with prior parental consent.
Exclusion
- • soft tissue inflammation.
- tooth mobility.
- sinus tract.
- Any radiographic sign of periapical pathologies or pulp necrosis (periapical radiolucency, internal or external root resorption)
- History of any systemic disease
- Teeth showing clinical or radiographic evidence of pulp degeneration
- Hemostasis not achieved within 5 minutes of pulp amputation, by direct contact with a wet cotton pellet before the material placement
- The remaining radicular tissue was non-vital (with suppuration or purulence necrosis)
Key Trial Info
Start Date :
September 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 15 2025
Estimated Enrollment :
28 Patients enrolled
Trial Details
Trial ID
NCT06524921
Start Date
September 1 2024
End Date
September 15 2025
Last Update
August 20 2024
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