Not yet recruiting NCT06903013
Post Operative Pain Following Pulpectomy Versus Pulpotomy in Primary Molars Wit Irreversible Pulpitis
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Non vitalPulp therapy, Vital pulp therapy.
- Who it may be relevant to
- Registry conditions: Irreversible Pulpitis. Basic parameters: 4 years — 10 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Post Operative Pain Following Pulpectomy Versus Pulpotomy in Primary Molars Wit Irreversible Pulpitis a Parallel Randomized Clinical Trial
Overview
Study will evaluate and compare post operative pain for primary molars with irreversible pulpitis after pulpotomy and pulpuectomy
Interventions
- Other Non vitalPulp therapy
Pulp therapy deals about management of inflamed vital dental pulp With complete pulp removal and obturation with resorbable materi - Other Vital pulp therapy
Pulp therapy through partial root removal and using of regenerative capping material
Primary outcome measures
- Post operative pain [Time frame: 6 months]
Eligibility criteria
Inclusion criteria
- Healthy individual
- Has primary tooth with irreversible pulpitis
- Cooperative child
Exclusion criteria
- Mentally, physically or medically compromised children
- Uncooperative children
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06903013 · 1029