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Clinical and Radiographic Success Rate of Pulpotomy Versus Pulpectomy for Management of Primary Teeth With Deep Caries

Cairo University (CU) logo

Cairo University (CU)

Status and phase

Not yet enrolling
Phase 2

Conditions

Deep Caries

Treatments

Procedure: Pulpotomy
Procedure: Partial Pulpectomy

Study type

Interventional

Funder types

Other

Identifiers

NCT06293521
06091995

Details and patient eligibility

About

This trial aims to compare treatment outcomes between Pulpotomy and Pulpectomy in treating vital primary teeth diagnosed with deep caries with symptoms of irreversible pulpits

Full description

Background: Pulpectomy is the reference treatment for vital primary molars with irreversible pulpitis.Over the past decades, dental caries has unfailingly been the most common chronic infectious disease of childhood and adults. If remained untreated, it can potentially compromise dental pulp tissue. When the dental pulp of primary teeth is irreversibly inflamed, the first treatment choice is pulpectomy, owing to the well-recognized importance of primary tooth retention for child oral/general health. Although a pulpless tooth can remain functional in the oral cavity, modern pediatric endodontics encourages regenerative approaches in primary teeth.The introduction of calcium silicate-based (CS-B) biomaterials such as mineral trioxide aggregate (MTA), along with further understanding of pulp biology and inflammatory processes, has revolutionized treatment modalities for management of irreversible pulpitis in mature permanent teeth. A growing body of evidence has revealed successful implementation of minimally invasive endodontics, that is, vital pulp therapies (VPTs) for management of permanent teeth with irreversible pulpitis even when associated with apical periodontitis. Due to the traditional notion of poorer healing capacity of primary dental pulp, such a paradigm shift has not been seen in pediatric dentistry.Recent research revealed similar vascular/immune responses of primary and permanent dental pulps to caries; therefore, indicating that their healing potential might be this in mind, a reevaluation of traditional approaches for treatment of inflamed primary pulp seems justified.

Enrollment

40 estimated patients

Sex

All

Ages

4 to 6 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Aged 4 to 6 years , in good general health
  2. The parents provided written informed consent.
  3. Clinical characteristics, defined as spontaneous pain and the presence of a deep carious lesion with pulp exposure and bleeding that did not halt within five minutes following removal of the coronal pulp tissue.
  4. Restorable teeth.

Exclusion criteria

  1. Physical or mental disability.
  2. Unable to attend follow-up visits.
  3. Previously accessed teeth.
  4. Swelling, tenderness to percussion or palpation, or pathological mobility.
  5. Pre-operative radiographic pathology such as resorption (internal or external), per-radicular or furcation radiolucency.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

MTA Pulpotomy
Experimental group
Description:
Intervention group
Treatment:
Procedure: Pulpotomy
Chlorohexidine Pulpectomy
Active Comparator group
Description:
Control group
Treatment:
Procedure: Partial Pulpectomy

Trial contacts and locations

1

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Central trial contact

Nada Mostafa, B.D.S

Data sourced from clinicaltrials.gov

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