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Post-operative Hyper-sensitivity Assessment After Immediate Versus Delayed Dentine Sealing in Teeth for Indirect Tooth Colored Restorations

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Hypersensitivity Dentin

Treatments

Procedure: Delayed dentin sealing protocol
Procedure: Immediate dentin sealing protocol

Study type

Interventional

Funder types

Other

Identifiers

NCT03562858
CEBD-CU-2018-05-21

Details and patient eligibility

About

PICOT elements:P: Teeth restored with indirect tooth colored restoration I: Immediate dentin sealing using universal adhesive C: Delayed dentin sealing O: Post-operative Hypersensitivity T: -Hypersensitivity assessment one week during provisionalization period and post-cementation S: Randomized Controlled Clinical Trial

Enrollment

54 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Extensive carious lesions indicated for indirect restorations
  • Lower first molars
  • Age of patients range is 18 -50 years
  • Patients have not received antibiotic therapy for 1 month before sampling
  • Males or Females (Both genders)
  • Patients with Good oral hygiene
  • Co-operative patients approving the trial

Exclusion criteria

  • Pregnancy
  • Systemic disease or severe medical
  • Patients having complications as:

Periodontal problems Mobile teeth, arrest caries and non-vital teeth

  • Heavy smoking patients
  • Xerostomia
  • Lack of compliance

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

54 participants in 2 patient groups

Delayed dentine sealing
Active Comparator group
Treatment:
Procedure: Delayed dentin sealing protocol
Immediate dentin sealing
Experimental group
Treatment:
Procedure: Immediate dentin sealing protocol

Trial contacts and locations

1

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Central trial contact

Hoda Fouda, Master

Data sourced from clinicaltrials.gov

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