About this trial
The goal of this interventional study is to evaluate the different materials used for pulpotomy procedures in deciduous molars. this will help us find out which medicament is more effective in releving which medicament is more effective in releving pain and resolution of signs of infection.it will help us find out less chair time for procedure and cooperation of child .
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Symptomless carious teeth with vital pulp exposure
No clinical sign/symptoms of spontaneous and nocturnal pain, and tenderness to percussion or palpation, history of swelling or sinus tracts, pathologic mobility.
Teeth restorable.
No radiographic evidence of pulp degeneration such as internal or external resorption, inter-radicular or periapical bone destruction.
Disqualifiers
Teeth diagnosed with irreversible pulpitis
Teeth having Pulp necrosis / periapical abscess
Teeth with previous pulp therapy(pulpotomy/pulpectomy)
Children with systemic medical conditions that may affect healing or contraindicate treatment.
Trial design
Single group
Treatments tested in this trial
FORMOCRESOL PULPOTOMY MATERIAL
DrugFORMOCRESOL PULPOTOMY MATERIAL FOR 5MINUTES PACKED WITH STERILE COTTON PELLETS ON PULP STUMPS FERRIC SULPHATE 15.5 % PACKED ON PULP STUMPS WITH STERILE COTTON PELLET FOR 15 SECONDS. MINERAL TRIOXIDE AGGREGATE PLACED ON PULP STUPMS
Treatment groups
Trial outcomes
Primary outcomes
PAIN RELIEF
PAIN RELIEF ASSESMENT BY SCALE 0-10 (O no pain ,1-3 mild pain, 4-7 moderate pain ,8-10 extreme pain)
Locations
Sponsors and contacts
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