Deep Carious Lesions

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Review clinical trials related to Deep Carious Lesions. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Comparative Evaluation of Calcium Silicate-doped Treated Dentin Matrix and Mineral Trioxide Aggregate as Miniature Pulpotomy Biomaterials in Deep Carious Lesions

AIM: To compare the efficacy of a Novel calcium silicate doped treated dentin matrix and Mineral Trioxide aggregate as biomaterials for miniature pulpotomy. OBJECTIVES: Primary objective: To evaluate the efficacy of calcium silicate-doped human-treated dentin matrix (CaSi+hTDM) compared to Mineral Trioxide Aggregate (MTA) in maintaining pulp vitality using cold testing following Miniature Pulpotomy (MP) in deep and extremely deep carious lesions with reversible pulpitis in 14- to 35-year-old patients reporting to Department of Dentistry, AIIMS Nagpur. Secondary objectives: 1. To evaluate patient-reported outcomes such as pain, swelling, sinus tract etc. post-operatively. 2. To determine the clinical success rates of both materials by assessing the Periapical index of healing over a 6 months follow-up period. NULL HYPOTHESIS: The null hypothesis (H0) is that there is no difference between CaSi+hTDM and MTA in maintaining pulp vitality when used as a Miniature Pulpotomy (MP) biomaterial in carious lesions.

Participants needed: 56
Trial details
Age: 14-35Biological sex: AllType: InterventionalSponsor: All India Institute of Medical SciencesUpdated: Mar 10, 2026Locations: 2
Eligibility criteria

The clinical diagnosis of reversible pulpitis characterized by mild pain (on Num... [+3]

A history of spontaneous unprovoked toothache, pain on percussion, a sinus tract... [+5]

Status: Not yet recruiting

This Study Aims to Clinically Assess and Radiographically Measure the Formed Dentin Bridge Over the Pulp, Utilizing Three-dimensional Imaging Following the Application of a Bioactive Restorative System Versus a Conventional Restorative System After Selective Caries Removal to Soft Dentin Over 2

This clinical trial aims to evaluate dentin bridge formation over the pulp following selective caries removal in permanent teeth with deep carious lesions (ICDAS scores 5-6). A total of 66 patients will be enrolled and randomly allocated to receive either a bioactive restorative system (bioactive universal adhesive combined with a bioactive bulk-fill resin composite) or a conventional non-bioactive restorative system. Clinical assessments, including pulp sensibility testing and patient-reported pain evaluation, together with three-dimensional radiographic analysis using cone beam computed tomography, will be conducted to assess the thickness and quality of reparative dentin bridge formation. Outcomes will be evaluated at baseline and during follow-up periods extending up to 24 months to compare the effectiveness of both restorative approaches in preserving pulp sensibility and promoting dentin-pulp complex repair.

Participants needed: 66
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Jan 21, 2026
Eligibility criteria

Adult patients (age: 18-40 years) of both genders. [+7]

Allergy to any of the restorative materials. [+10]

Status: Not yet recruiting

Clinical and Radiographic Evaluation of Indirect Pulp Capping Using Platelet Rich Fibrin Versus Mineral Trioxide Aggregate in Deep Carious Molars: a Randomized Controlled Trial

The aim of this study is the clinical and radiographic evaluation of (Platelet-Rich Fibrin (PRF) versus Mineral Trioxide Aggregate (MTA) in indirect pulp capping when used with deep carious molars over 1 year follow up.

Participants needed: 50
Trial details
Phase: Phase 2Age: 20-40Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Mar 21, 2025Locations: 1
Eligibility criteria

o Patients with asymptomatic deep carious molars. [+7]

o Patients with systemic conditions affecting bone or tissue healing (e.g., unco... [+11]

Status: Not yet recruiting

Clinical Performance of Resin Composite Restoration After Dentin Biomodification by Grape Seed Extract in Deep Carious Lesions.

This study will evaluate the clinical and radiographic performance of resin composite restoration after utilized a grape seed extract as dentin biomodification in vital teeth with deep occlusal carious lesions (ICDAS 5-6) after selective soft dentin removal technique.

Participants needed: 60
Trial details
Age: 22-42Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Jan 17, 2025
Eligibility criteria

Adult patients (age: 22-42 years) of both genders. [+7]

Allergy to any of the restorative materials. [+10]