About this trial
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?
Eligibility criteria
Qualifiers
Restorable mandibular primary molars.
History of reversible pulpitis.
Absence of periapical or inter-radicular radiolucencies.
Absence of widening of periodontal ligaments (PDL) space.
Disqualifiers
With systemic disorders.
Physical or mental disabilities.
Unable to attend follow- up visits.
Refusal of Participation.
Trial design
Treatments tested in this trial
- Hyaluronic acid pulpotomy
- mineral trioxide aggregate pulpotomy