Clinical & Radiographic Efficacy Using LLLT & CRYO on M.P.M Pulpotomy
ConditionMTA Vital Tooth Pulpotomy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age15-60
SponsorTanta University
About this trial
This in-vivo study aims to evaluate the efficacy of the low level laser therapy and cryotherapy in treatment of vital pulpotomy in mature permanent molar evaluating the post operative pain and the radiographic changes in pulpal and periodontal regions.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
• Restorable vital and mature mandibular molar teeth with irreversible pulpitis.
Teeth with deep caries or large restoration.
Pre-operative radiograph showing normal periapical structure.
Teeth with normal periodontal status .
Disqualifiers
• Medically compromised patients with active systemic disease as uncontrolled diabetes mellitus, hypertension or cardiac diseases.
Teeth with periapical lesion.
Sinus tract or swelling.
Moderate or severe marginal periodontitis.
Trial design
Design model
Parallel
Treatments tested in this trial
low level laser device cryotherapy
Deviceusing new device direct on the pulp tissue
Treatment groups
30 Participants
are divided into 3 treatment groupsGroup A: • Group I: Conventional complete Pulpotomy using MTA (control group).No intervention 0 interventions
Group B: • Group II: LLLT following complete pulpotomy.Active comparator 1 intervention
Group C: • Group III: Cryotherapy following complete pulpotomy.Active comparator 1 intervention
Trial outcomes
Primary outcomes
1
radiographic changes
and x-ray change either pulpal or periapical using CBCT subtraction
Time frame
one year after treatmentSecondary outcomes
1
Post operative pain
Post operative pain using visual analog scale by the patient description pain on his own words
Time frame
one week after treatmentSponsors and contacts
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Source ClinicalTrials.gov