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

Post-operative Hyper-sensitivity Assessment After Immediate Versus Delayed Dentine Sealing in Teeth for Indirect Tooth Colored Restorations: Randomized Controlled Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03562858
Enrollment
54
Registered
2018-06-20
Start date
2018-07-31
Completion date
2018-10-31
Last updated
2018-06-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypersensitivity Dentin

Brief summary

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

Interventions

PROCEDUREImmediate dentin sealing protocol

Sealing of the dentin before impression taking directly after cavity preparation to prevent postoperative hypersensitivity during provisionalization and after cementation

PROCEDUREDelayed dentin sealing protocol

Sealing the dentin just prior to cementation

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Post-operative hypersensitivity at baseline10 minutesThe post-operative hypersensitivity assessment will be performed at baseline , using visual analogue scale (VAS) for both intervention and control group . The visual analogue scale is a scale numbered from zero to 10 , where as the range from zero to three resembles from no to very mild sensitivity , the range from four to seven resembles moderate sensitivity and from eight to ten resembles severe sensitivity
Post-operative hypersensitivity one week after temporization1 weekThe post-operative hypersensitivity will be assessed one week after temporization for both intervention and control group using the visual analogue scale VAS .The visual analogue scale is a scale numbered from zero to 10 , where as the range from zero to three resembles from no to very mild sensitivity , the range from four to seven resembles moderate sensitivity and from eight to ten resembles severe sensitivity
Post-operative hypersensitivity after cementation of the indirect tooth coloured restoration1 weekThe post-operative hypersensitivity will be assessed using visual analogue scale VAS 1 week after cementation of the indirect tooth coloured restoration. The visual analogue scale is a scale numbered from zero to 10 , where as the range from zero to three resembles from no to very mild sensitivity, the range from four to seven resembles moderate sensitivity and from eight to ten resembles severe sensitivity

Countries

Egypt

Contacts

Primary ContactHoda Fouda, Master
Hoda.omar@dentistry.cu.edu.eg01003786531

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026