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Clinical Trials/CTRI/2025/04/084958
CTRI/2025/04/084958Not yet recruitingNot Applicable

Comparative evaluation of postoperative sensitivity in non-carious cervical lesions restored with composite using step curing vs continuous curing modes of LED: A split-mouth randomised controlled single-blind trial

Dr Pooja Shah1 site in 1 country30 target enrollmentStarted: April 20, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Post operative sensitivity scores

Study Overview

Brief Summary

Post-operative sensitivity after composite restoration remains a challenge and in most studies postoperative sensitivity was found to be up to onethird of the study sample· Non carious cervical lesions [NCCL] cause loss of dental hard tissue in the cervical part of the tooth exposing the dentinal tubules to the oral environment. · Thus, when the affected tooth is exposed to heat or stimuli, it results in expansion and contraction of dentinal fluids in the gap formed, which causes fluid movement in the dentinal tubules leading to postoperative sensitivity. · Flowable resins tend to absorb the stresses created during polymerization shrinkage. G-aenial Universal Flow, a flowable resin tends to exhibit lower polymerization shrinkage stress of about 1.3 MPa, which leads to lesser postoperative sensitivity.· It is claimed that soft start polymerization technique reduces polymerization shrinkage sequentially reducing microgaps, microleakage, and postoperative sensitivity. Thus we have undertaken this study comparing postoperative sensitivity using G-aenial Universal Flo with step curing and continuous curing technique in NCCL · Hence this study will highlight if step curing is a better treatment modality than continuous curing in reducing postoperative sensitivity in NCCL, so that a better technique can be adopted in subsequent patients.

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
Participant Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Cooperative, healthy subjects who are willing to participate in the study and sign the consent form.
  • Selected subjects must be at least 18 years old and of either sex.
  • Subjects having NCCLs involving enamel and dentin.
  • Subjects having at least two contra lateral teeth with Non carious cervical lesion.
  • Vital teeth giving a positive response to cold test.

Exclusion Criteria

  • Subjects unwilling to sign the consent form.
  • Teeth with carious lesions.
  • Subjects with teeth having lesions more than 2 mm in depth.
  • NCCLs extending below the cemento-enamel junction.
  • Patients using desensitizing agents regularly.
  • Teeth with spontaneous, severe or continuous pain and existing sensitivity.
  • Patients with any irreversible pulpal, periodontal and periapical pathology.
  • Patients having bruxism.

Outcomes

Primary Outcomes

Post operative sensitivity scores

Time Frame: Post operative sensitivity scores at 24 hours, 7 days and 1 month

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Dr Pooja Shah
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr Pooja Shah

Bharati Vidyapeeth Dental College and Hospital, Navi Mumbai

Study Sites (1)

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