Partial Versus Miniature Pulpotomy in Teeth With Irreversible Pulpitis

  • STATUS
    Recruiting
  • End date
    Jul 14, 2023
  • participants needed
    86
  • sponsor
    Postgraduate Institute of Dental Sciences Rohtak
Updated on 14 June 2022
Accepts healthy volunteers

Summary

This study will compare the outcome of partial and miniature pulpotomy in mature permanent molars with symptomatic partial irreversible pulpitis

Description

After thorough history and clinical and radiographic examination, and confirmation of eligibility for the study, written informed consent will be obtained from study participants after explaining the procedure and its associated risks and benefits. Clinical diagnosis of symptomatic partial irreversible pulpitis will be established based on a history of spontaneous pain or pain exacerbated by cold stimuli and lasting for a few seconds to several hours (lingering pain) compared to control teeth and which is reproducible using cold testing.

Once included, study subjects will be randomly allocated to either Miniature Pulpotomy group or Partial Pulpotomy group. MTA (Mineral Trioxide Aggregate) will be used as pulpotomy agent. A layer of resin modified Glass Ionomer liner will be placed over the MTA and tooth will be permanently restored with composite resin in same appointment.

Pain analysis will be carried out preoperatively and postoperatively at every 24 hours till 7 days after intervention. All the subjects will be followed up for evaluation of clinical and radiographic success at 6 and 12 months from baseline.

Details
Condition Pulpitis - Irreversible
Treatment partial pulpotomy, Miniature pulpotomy
Clinical Study IdentifierNCT05406557
SponsorPostgraduate Institute of Dental Sciences Rohtak
Last Modified on14 June 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

The patient with18 -45 years of age
Restorable molar teeth
Tooth should give positive response to pulp sensibility testing
Clinical diagnosis of symptomatic partial irreversible pulpitis
Tooth with probing pocket depth and mobility are within normal limits
No signs of pulpal necrosis including sinus tract or swelling
Non-contributory medical history

Exclusion Criteria

Teeth with immature roots
No pulp exposure after caries excavation
Bleeding could not be controlled in 6 minutes
Insufficient bleeding after pulp exposure, the pulp is judged necrotic or partially necrotic
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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