To Evaluate Periapical Healing Post Full Pulpotomy in Teeth With and Without Apical Periodontitis

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorPostgraduate Institute of Dental Sciences Rohtak

About this trial

This clinical study aims to evaluate the periapical and clinical healing outcomes of full pulpotomy using MTA in mandibular permanent molars diagnosed with symptomatic irreversible pulpitis. Patients will be stratified based on the presence or absence of apical periodontitis. Clinical and radiographic assessments will be conducted at baseline, 6 months, and 12 months to compare healing outcomes between groups. The study seeks to determine the effectiveness of full pulpotomy as a less invasive alternative to root canal treatment, even in teeth with apical pathosis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

The patient should be ≥18 years of age.

Restorable mature permanent 1st and 2nd Mandibular molars with extremely deep caries (≥2/3 dentine involvement)

Tooth should give positive response to pulp sensibility testing.

Radiographic finding of periapical index (PAI) score >/=3 (for test group) , score </= 2 (for control group)

Disqualifiers

Teeth with immature roots.

No pulp exposure after caries excavation.

Bleeding could not be controlled in 10 minutes.

Signs of pulpal necrosis, sinus tract, swelling, insufficient bleeding after pulp exposure.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Full pulpotomy in adults ≥18 years with restorable mandibular first or second molars diagnosed with irreversible pulpitis, with or without apical periodontitis.

    Procedure/Surgery

    Comparison of full pulpotomy with MTA in teeth with and without apical periodontitis

Treatment groups

128 Participants
are divided into 2 treatment groups
Group A: To evaluate success of full pulpotomy in mandibular permanent with apical periodontitisExperimental treatment 1 intervention
Group B: To evaluate success of full pulpotomy in mandibular permanent without apical periodontitisExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Success following complete pulpotomy

Clinical-Radiographic Success After Full Pulpotomy in Mandibular Molars With and Without Apical Periodontitis"

Time frame
12 MONTHS

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: