ClinConnect ClinConnect Logo
Search / Trial NCT06904781

Treatment Outcomes of Pulpotomy Versus Pulpectomy in Vital Primary Molars Diagnosed With Irreversible Pulpitis

Launched by QATAR UNIVERSITY · Mar 25, 2025

Trial Information

Current as of July 23, 2025

Not yet recruiting

Keywords

Pulpectomy Pulpotomy Vital Primary Molars Irreversible Pulpitis

ClinConnect Summary

This clinical trial is studying two different dental treatments, pulpotomy and pulpectomy, to see which one works better for treating young children with a condition called irreversible pulpitis, which means that the nerve inside a tooth is damaged and causing pain. Pulpotomy is a simpler and quicker procedure that can be easier for kids to handle, while pulpectomy is the more traditional approach. The researchers want to find out if pulpotomy can effectively treat the problem while making the experience more comfortable for young patients.

To be eligible for this trial, children aged between four and nine years old who are healthy and cooperative may participate, as long as they have a primary molar (a back tooth) showing symptoms of irreversible pulpitis, but without signs of infection. Parents should be willing to have their child's tooth covered with a crown after treatment. Participants in the trial can expect to receive one of the two treatments and will be part of a study that aims to improve dental care for children in the future. This trial is not yet recruiting participants, so there is no immediate action needed.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Healthy (ASA I and II) co-operative children (Frankl Scale + and ++) between the ages of four and nine years.
  • 2. Participants have symptoms typical of irreversible pulpitis in one of the primary molars.
  • 3. The pulp of the affected primary molar is vital.
  • 4. Radicular pulp health is confirmed by attainment of radicular pulp haemostasis within 6 minutes of coronal pulp amputation.
  • 5. The affected primary molars can be restored with full coverage stainless steel crowns.
  • 6. Any physiologic root resorption, if present, is less than ⅓ the root length.
  • Exclusion Criteria:
  • 1. Clinical examination of affected primary molar reveals signs of pulpal infection (e.g. pathologic tooth mobility, parulis/fistula, or soft tissue swelling).
  • 2. Pre-operative periapical radiograph suggests presence of periapical radiolucency or pathologic root resorption.
  • 3. Visual examination of pulp tissue after deroofing reveals signs of necrosis (e.g. avascular/minimally bleeding pulp tissue or yellowish necrotic areas/purulent exudate).
  • 4. Signs of extensive radicular pulp inflammation i.e., root pulp bleeding continues even after 6-min.
  • 5. Parents not willing to place full coverage crowns post-treatment.
  • 6. Clinical diagnosis of irreversible pulpitis between two adjacent primary molars is not sharply defined.
  • 7. Unable to perform clinical procedure under rubber dam

About Qatar University

Qatar University is a leading academic institution dedicated to advancing research and innovation across various fields, including healthcare and clinical sciences. As a clinical trial sponsor, Qatar University leverages its robust academic resources and expertise to conduct rigorous research aimed at improving health outcomes and addressing public health challenges. The university fosters collaboration among multidisciplinary teams, promoting the integration of cutting-edge scientific knowledge with practical applications. Through its commitment to ethical research practices and adherence to regulatory standards, Qatar University aims to contribute meaningful insights to the global medical community while enhancing the quality of care for diverse populations.

Locations

Patients applied

0 patients applied

Trial Officials

Nebu Philip, MDS, PhD

Principal Investigator

Qatar University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported