Pulpotomies Primary Teeth

3

Review clinical trials related to Pulpotomies Primary Teeth. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Comparison of Hyaluronic Acid, TheraCal, and Mineral Trioxide Aggregate as Pulpotomy Agents in Primary Molars

This randomized clinical trial aims to evaluation the clinical and radiographic outcomes of hyaluronic acid, TheraCal, and Mineral Trioxide Aggregate (MTA) when used as pulpotomy agents in primary molars. The main question it aims to answer is: In children with restorable mandibular second primary molars requiring pulpotomy, does the use of hyaluronic acid or TheraCal LC, compared to MTA, result in improved clinical and radiographic success rates over a 12-month follow-up period?

Participants needed: 66
Trial details
Age: 4-8Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Sep 11, 2025Locations: 1
Eligibility criteria

Age 4-8 years, [+9]

Swelling, sinus tract, or fistula. [+7]

Status: Not yet recruiting

Clinical and Radiographic Evaluation of Potassium Nitrate in Polycarboxylate Versus Mineral Trioxide Aggregate in Vital Pulpotomy in Primary Molars

The purpose of this RCT is to compare the clinical/radiographic outcomes of Potassium nitrate in polycarboxylate cement and MTA as pulpotomy biomaterials used for asymptomatic vital primary lower second molar and this will help to clinically evaluate the use of alternative material in vital pulpotomy in primary molars with deep carious cavities. Emphasis is set on avoiding total pupectomy and maintaining radicular pulp vitality therefore maintain the tooth in a viable condition till it's shedding and eruption of the permanent successor.

Participants needed: 50
Trial details
Age: 4-7Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Mar 12, 2025Locations: 1
Eligibility criteria

Children aged 4 to 7 years, in good general health. [+6]

Children with a physical disability or medical disability. [+5]

Status: Not yet recruiting

Clinical and Radiographic Evaluation of Hyaluronic Acid (Gengigel Teething) Versus Mineral Trioxide Aggregate( Angelus) as Pulpotomy Agent in Vital Primary Molars

The goal of this clinical trial is to Clinical and Radiographic Evaluation of Hyaluronic Acid (Gengigel Teething) Versus Mineral Trioxide Aggregate( Angelus) as Pulpotomy Agent in Vital Primary Molars. The main question it aims to answer is: Is there a difference in the clinical or radiographic success when using Hyaluronic acid (Gengigel Teething, Ricerfarma , Italy) versus mineral trioxide aggregate (Angelus, Londrina ,Brazil) in pulpotomy of carious primary molars in children?

Participants needed: 34
Trial details
Phase: Phase 1Age: 4-8Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Nov 4, 2024Locations: 1
Eligibility criteria

Restorable mandibular primary molars. [+4]

With systemic disorders. [+8]