Clinical Trials Directory

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UnknownNCT04374214

Effect of Simvastatin as Pulpotomy Agent in Cariously Exposed Permanent Molars

Effect of Simvastatin on Success of Pulpotomy in Cariously Exposed Permanent Molars: a Randomized Control Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
56 (estimated)
Sponsor
Postgraduate Institute of Dental Sciences Rohtak · Academic / Other
Sex
All
Age
15 Years – 40 Years
Healthy volunteers
Accepted

Summary

The study will compare the outcome of complete pulpotomy in mature permanent mandibular molars with deep carious lesions by using Mineral Trioxide Aggregate and Simvastatin -alpha tricalcium phosphate as medicament agent

Detailed description

After a thorough history, clinical and radiographic examination with all eligibility confirmation, written informed consent will be taken from the patient after explaining the procedure, its associated risks and benefits. Clinical diagnosis of reversible pulpitis will be established. Complete pulpotomy will be done in both groups. Mineral Trioxide Aggregate and Simvastatin -alpha tricalcium phosphate will be used as pulpotomy agents. Pain analysis will be carried out preoperatively and postoperatively at every 6 hours for 1 day and then every 24 hours till 7 days after the intervention. All the subjects will be followed up for evaluation of clinical and radiographic success at 3, 6 months and 1 year.

Conditions

Interventions

TypeNameDescription
PROCEDUREComplete Pulpotomy using Mineral Trioxide AggregateInflammed coronal pulp tissue will be removed till the canal orifices and mineral trioxide aggregate placed over the amputated pulp stump.
PROCEDUREComplete Pulpotomy using Simvastain -alphatricalcium phosphateInflammed coronal pulp tissue will be removed till the canal orifices and Simvastatin -alpha tricalcium phosphate placed over the amputated pulp stump.

Timeline

Start date
2018-12-01
Primary completion
2020-04-30
Completion
2020-06-30
First posted
2020-05-05
Last updated
2020-05-05

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT04374214. Inclusion in this directory is not an endorsement.