Direct Pulp Capping Agent on Human Pulp Tissue

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE4

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-01

Study Completion Date

2024-07-31

Brief Summary

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This in- vivo study was conducted to evaluate the response of human pulp tissue following direct pulp capping using four different pulp capping agents in premolars scheduled for extraction in patients undergoing orthodontic treatment.

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Detailed Description

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For the study 40 premolars from patients in the age group of 15-25 years, undergoing orthodontic treatment, in the Department of Orthodontics, MMCDSR, Mullana, Ambala, who had to get their premolars extracted as per their orthodontic treatment plan will be selected.

Only healthy premolars, with no caries, showing no signs and symptoms of pulpitis or periodontal diseases were selected. Medically compromised patients, or teeth with radiographic findings of external/internal resorption, bone loss, or calcifications in the pulp chamber will be excluded from the study. The selected premolars were then randomly divided into four equal groups namely: GROUP I - Direct pulp capping procedure performed using Biodentine. GROUP II - Direct pulp capping procedure performed using MTA. GROUP III - Direct pulp capping procedure performed using TheraCal LC. GROUP IV - Direct pulp capping procedure performed using Tristrontium aluminate.

The direct pulp capping procedure was carried out under rubber dam. The study protocol included class I cavity preparations on the premolars, followed by iatrogenic exposure of the pulp (0.5mm) using a sterile round bur, placement of the direct pulp capping agent according to the material of allotted to the study group. The teeth were permanently restored on the same visit, except for MTA group were the teeth were temporarily restored using Cavit G, and recalled after 1 day for permanent restoration. The patients were then enquired for any 94 SUMMARY 95 symptoms at 1 day and 7 days post operatively. The teeth were then, atraumatically extracted 3 months after the procedure. The extracted teeth were then put to CBCT as well as histopathological examination. Through CBCT evaluation, the completeness of the dentine bridge was evaluated. Histopathological examination was done to examine the pulpal response and the quality of the dentine bridge formed

Conditions

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Reversible Pulpitis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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BIODENTINE

DIRECT PULP CAPPING WILL BE DONE USING BIODENTINE AS DIRECT PULP CAPPING AGENT

Group Type SHAM_COMPARATOR

Biodentine

Intervention Type DRUG

DIRECT PULP CAPPINGWILL BE DONE USING BIODENTINE

MINERAL TRIOXIDE AGGREGATE

DIRECT PULP CAPPING WILL BE DONE USING MTA AS DIRECT PULP CAPPING AGENT

Group Type SHAM_COMPARATOR

Mineral Tri-Oxide Aggregate

Intervention Type DRUG

DIRECT PULP CAPPINGWILL BE DONE USING MTA

THERACAL LC

DIRECT PULP CAPPING WILL BE DONE USING THERACAL LC AS DIRECT PULP CAPPING AGENT

Group Type SHAM_COMPARATOR

THERACAL LC

Intervention Type DRUG

DIRECT PULP CAPPINGWILL BE DONE USING THERACAL LC

TRISTRONTIUM ALUMINATE

DIRECT PULP CAPPING WILL BE DONE USING TRISTRONTIUM ALUMINATE AS DIRECT PULP CAPPING AGENT

Group Type ACTIVE_COMPARATOR

TRISTRONTIUM ALUMINATE

Intervention Type DRUG

DIRECT PULP CAPPINGWILL BE DONE USING TRISTRONTIUM ALUMINATE

Interventions

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Biodentine

DIRECT PULP CAPPINGWILL BE DONE USING BIODENTINE

Intervention Type DRUG

Mineral Tri-Oxide Aggregate

DIRECT PULP CAPPINGWILL BE DONE USING MTA

Intervention Type DRUG

THERACAL LC

DIRECT PULP CAPPINGWILL BE DONE USING THERACAL LC

Intervention Type DRUG

TRISTRONTIUM ALUMINATE

DIRECT PULP CAPPINGWILL BE DONE USING TRISTRONTIUM ALUMINATE

Intervention Type DRUG

Other Intervention Names

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MTA

Eligibility Criteria

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Inclusion Criteria

* CARIES-free, undamaged mature maxillary and mandibular premolars that were planned for extraction for orthodontic reasons.
* Teeth that show no reaction to percussion.
* Teeth with no previous restorations.
* Teeth that show vitality, when checked with an electric pulp tester.
* Teeth that show no signs of caries or periapical pathology when examined
* radiographically.
* Fully erupted teeth, that allowed proper application of rubber dam.

Exclusion Criteria

* caries are present
* Teeth with signs and symptoms of irreversible pulpitis, such as nighttime severe pain
* or spontaneous pain.
* Teeth that show sensitivity to hot and/or cold.
* Radiographic examination reveals any signs of caries, periapical pathology,
* internal/external root resorption, furcal radiolucency/ inter-radicular bone destruction
* and/or calcifications in the pulp chamber or canals.
* Medically compromised patient.
* Pregnant patient.

Minimum Eligible Age

15 Years

Maximum Eligible Age

25 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes