CompletedPhase 4

Postoperative Sensitivity Following Placement with Different Restorative Materials in Vital Posterior Teeth

Pakistan160 participantsStarted 2023-06-01

Plain-language summary

There is a lack of long-term clinical studies comparing different restorative materials; most of the available studies have only looked at class I cavities or examined post-operative sensitivity in non-caries cervical lesions. The purpose of this study is to measure postoperative sensitivity in clinical settings at 3-month intervals for class 1 and 2 direct posterior restoration

Who can participate

Age range18 Years – 40 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Either gender Minimum age 18 years, maximum age 40 years. Class I \& II Cavity on maxillary and mandibular 1st and 2nd molars. Vital maxillary and mandibular molar teeth that had occlusal contact with antagonist teeth. Exclusion Criteria: Irreversible Pulpitis diagnosed clinically and radiographically. Class I \& Class II cavity of premolars and third molars Patients taking analgesic prior to treatment. History of allergic reaction to any dental material used in the study. History of parafunctional habits (bruxism and/or clenching) Malocclusion

What they're measuring

Post Operative Sensitivity

Timeframe: 3 Months

Trial details

NCT IDNCT05882760

SponsorLiaquat University of Medical & Health Sciences

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-09-30

View on ClinicalTrials.gov More Sensitivity, Tooth trials