Evaluation of Pulpotomy Techniques (Formocresol, Ferric Sulphate, Mineral Trioxide Aggregate)

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age4-9
SponsorFoundation University Islamabad

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 volunteers

Qualifiers

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

Design model

Single group

Treatments tested in this trial

  • FORMOCRESOL PULPOTOMY MATERIAL

    Drug

    FORMOCRESOL 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

120 Participants
are divided into 1 treatment group
Group A: PULPOTOMY MATERIALExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

PAIN RELIEF

PAIN RELIEF ASSESMENT BY SCALE 0-10 (O no pain ,1-3 mild pain, 4-7 moderate pain ,8-10 extreme pain)

Time frame
2WEEKS ,1 MONTH ,6 MONTHS

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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