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Effect of Liners on Pulpal Outcome and Restoration Survival After Partial Caries Excavation

P

Postgraduate Institute of Dental Sciences Rohtak

Status

Completed

Conditions

Reversible Pulpitis

Treatments

Procedure: PCR with RMGIC
Procedure: PCR with calcium hydroxide
Procedure: PCR with direct composite

Study type

Interventional

Funder types

Other

Identifiers

NCT03286959
Shreyasingh

Details and patient eligibility

About

Aim of the study was to determine the effectiveness of cavity liners regarding survival of restoration beneath composite restoration after partial caries removal in permanent teeth with deep caries and to evaluate and compare the pulp vitality outcome both clinically and radiologically with and without liners.

Study was conducted in Post Graduate Institute of Dental Sciences, Rohtak in department of Conservative Dentistry & Endodontics. Mature permanent mandibular molars with deep dentinal caries and without any signs of irreversible pulpitis were included in the study. After partial excavation of caries, patients were randomly allocated into three groups- RMGIC, CH and DIRECT COMPOSITE group and were restored according to standard protocol.

Full description

AIM AND OBJECTIVES The present study aims to

  1. Evaluate the success of partial caries excavation in mandibular molar teeth.
  2. Evaluate and compare the clinical and radiographic success with RMGIC, calcium hydroxide and without liners after partial caries excavation.
  3. Evaluate and compare the effect of liners on restoration survival after partial caries excavation.

MATERIALS AND METHODS Study subjects were recruited from OPD of Department of conservative dentistry and endodontics, PGIDS, Rohtak.

METHODOLOGY Prior to treatment, a thorough clinical and radiological examination was carried out and a thorough history was taken.

Clinical procedure:

Mature mandibular permanent molars exhibiting deep caries involving more than half or two thirds of dentin were chosen for the study.

The teeth were evaluated by periapical radiographs, periodontal probing, percussion test, and vitality assessment with thermal test and electric pulp test; teeth determined to have reversible pulpitis were included and with irreversible pulpitis were excluded.

All periapical radiographs were exposed by using constant kVP, mA, and exposure time (70 KVP, 8 mA, and 0.8 sec.) with a Rinn paralleling device.

After administration of local anesthesia, rubber dam isolation of the involved tooth was done and tooth was swabbed with betadiene. Carious tissue from lateral walls and dentino enamel junction was removed completely while a layer of soft carious dentin was left adjacent to pulpal or axial wall followed by cleaning with distilled water and drying with sterile filter paper. Then the teeth were randomised into three groups using a computer generated sheet.

GROUP I CH GROUP- The pulpal or axial wall was lined by a layer of dycal as per manufacturer directions and restored with composite restoration using incremental technique.

GROUP II RMGIC GROUP - A layer of resin modified GIC was placed adjacent to pulpal or axial wall and tooth restored as above.

GROUP III DIRECT COMPOSITE GROUP- Tooth was restored with composite restorations as above without placing any liner.

FOLLOW UP- The patients were recalled periodically at 1 month, 3 months, 6 months and 12 months after the procedure for clinical (post operative sensitivity, pain, tenderness, vitality) and radiographic (widening of periodontal ligament space and periapical radiolucency) evaluation. Also, the restoration survival was assessed using modified Hickel criteria where marginal staining, marginal adaptation, fractures and retention, secondary caries and post operative sensitivity were evaluated.

CRITERIA FOR SUCCESSFUL PULPAL OUTCOME A positive vitality test. No pain on percussion. No widening of periodontal ligament on periapical radiograph. No clinical or radiographic signs and/or symptoms of irreversible pulpitis and pulp necrosis.

CRITERIA FOR FAILURE No response to pulp vitality test. Teeth exhibiting clinical or radiographic signs and/or symptoms of irreversible pulpitis and pulp necrosis.

Enrollment

198 patients

Sex

All

Ages

14 to 54 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient willing to participate in the study.
  • Mature permanent mandibular molars with deep dentinal caries involving more than half or two thirds of dentin.

Exclusion criteria

  • Primary teeth.
  • Teeth with irreversible pulpitis (spontaneous pain) or pulp necrosis, chronic periodontitis, cracked tooth, internal or external resorption, calcified canals, associated with sinus tract, and furcation or apical radiolucency.
  • Immuno-compromised, diabetic, pregnant and hypertensive patients.
  • Positive history of antibiotic and analgesic use.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

198 participants in 3 patient groups

PCR WITH CALCIUM HYDROXIDE
Active Comparator group
Description:
PCR WITH CALCIUM HYDROXIDE : A layer of dycal (dentsply) was placed adjacent to pulpal or axial wall after mixing as per manufacturer recommendations followed by etching and restoration with composite using incremental technique.
Treatment:
Procedure: PCR with calcium hydroxide
PCR WITH RMGIC
Active Comparator group
Description:
PCR WITH RMGIC: A layer of resin modified liner ( GC Fuji II ) was placed adjacent to pulpal or axial wall and light cured for 40 sec. afterwards the cavity was restored with composite as in other groups.
Treatment:
Procedure: PCR with RMGIC
PCR WITH DIRECT COMPOSITE
Active Comparator group
Description:
PCR WITH DIRECT COMPOSITE: After partial caries excavation , etching and bonding was done directly without using any liner and cavity was restored with composite as in other groups
Treatment:
Procedure: PCR with direct composite

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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