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Efficacy of PRF and MTA as Compared to Calcium Hydroxide for Pulpotomy in Human Irreversibly Inflamed Permanent Teeth

L

Liaquat College of Medicine and Dentostry

Status and phase

Completed
Phase 2

Conditions

Tooth Decay
Pulpitis - Irreversible

Treatments

Other: MTA
Other: PRF
Other: Calcium hydroxide

Study type

Interventional

Funder types

Other

Identifiers

NCT05266859
EC/13/17

Details and patient eligibility

About

Of all the various pulpotomy medicaments that have been studied till to date, three agents have been selected for this study to compare their efficacy. CH being the control, MTA being one of the most recommended biomaterial and PRF that in addition to being a biomaterial is an autologous agent. Uptil now there have been no prospective trials using these three pulpotomy agents in mature permanent teeth with irreversible pulpitis in our part of the world and even the international studies that have been done utilized different methodologies with no unanimous conclusion. This is the reason that at present this treatment regime (pulpotomy) showing better perspectives cannot be presented with confidence as a predictable treatment option to the patients with irreversible pulpitis. By virtue of this study this challenge is being undertaken.

Hypothesis:

ALTERNATE HYPOTHESIS There is a difference between the efficacy of the PRF, MTA and CH when used as pulpotomy medicaments in mature permanent teeth with irreversible pulpitis NULL HPOTHESIS There is no difference in efficacy of the PRF, MTA and CH when used as pulpotomy medicaments in mature permanent teeth with irreversible pulpitis

Enrollment

114 patients

Sex

All

Ages

10 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with permanent teeth with completely formed roots diagnosed with irreversible pulpitis i.e. showing signs and symptoms as spontaneous, lingering pain initiated by hot and cold stimulus and /or radiating. Pulp being exposed or near to exposure by caries or alternatively by trauma.

Exclusion criteria

  • CLINICALLY Teeth with

    • Necrotic pulp
    • History of swelling, abscess , fistula and/ or sinus tract
    • Doubtful restorability as indicated by over all Dental Practicality Index- (DPI) > 2 (Dawood and Patel 2017) will be excluded
    • Periodontal disease
    • Uncontrolled bleeding (more that 10 mins.) of pulp after removal of inflamed part.
    • No bleeding of pulp at all after access into pulp RADIOGRAPHICALLY (with the use of periapical radiographs) Teeth with
    • Internal/ external pathologic root resorption
    • Pulp canal obliteration
    • Periapical / furcal radiolucency
    • Resorbed roots.
    • Crestal bone loss Generally patients
    • With systemic diseases, bleeding disorders, physical or mental disability, pregnant or nursing.
    • On opioid or steroid therapy or anticoagulants and/or on any kind of antibiotics.
    • Who have gone through some previous treatment for the same tooth other than filling.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

114 participants in 3 patient groups

Group I- Calcium hydroxide (Control)
Active Comparator group
Description:
Group I will receive Calcium hydroxide . Calcium hydroxide is a gold standard medicament for the pulpotomy in deciduous teeth. It has antibacterial effects and widely used to disinfect the root canals. This group will act as a control
Treatment:
Other: Calcium hydroxide
Group II- MTA (Experimental)
Experimental group
Description:
Group II will receive MTA (Mineral Trioxide Aggregate). MTA is a calcium silicate based highly biocompatible material that is commonly used for pulpotomies in deciduous teeth along with the regenerative procedures in permanent and deciduous teeth
Treatment:
Other: MTA
Group III- PRF (Experimental)
Experimental group
Description:
Group III will receive PRF. PRF is platelet-rich fibrin that is a biocompatible product derived from patient's own blood. It is formed by centrifugation of the blood of the patient. It provides the growth factors and promotes regeneration of the pulp
Treatment:
Other: PRF

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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