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COMPARISON BETWEEN THE EFFECTS OF LOW-LEVEL LASER THERAPY AND CRYOTHERAPY ON POST-ENDODONTIC PAI

Phase 3
Conditions
Oral Health
Registration Number
PACTR202204787113528
Lead Sponsor
ODUKOYA ALABI ADETOUN OLUWAFEMI
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
105
Inclusion Criteria

•Subjects who are willing to give informed consent and abide by the protocol of the research
•Well-motivated subjects
•Permanent teeth (except third molars) with matured apex
•Carious permanent teeth (except third molars) with symptoms of irreversible pulpitis
• Carious permanent teeth (except third molars) with acute apical periodontitis characterised by tenderness to percussion clinically. Radiographically, normal periodontal ligament space and lamina dura
•Carious permanent teeth (except third molars) with acute apical periodontitis characterised by tenderness to percussion clinically. Radiographically, loss of lamina dura around the apex and periodontal ligament space widening
•Carious permanent teeth (except third molars) with acute apical periodontitis characterised by tenderness to percussion clinically. Radiographically, small sized periapical radiolucency and loss of lamina dura.
•Symptomatic carious permanent teeth (except third molars) requiring single-visit root canal treatment

Exclusion Criteria

•Subjects that are chronically ill that cannot tolerate a long dental procedure
•Subjects with poorly controlled systemic conditions like poorly-controlled hypertension or diabetes
•Pregnant females
•Uncooperative patients
•Patients with poor oral hygiene that cannot be improved within a limited time
•Teeth with insufficient periodontal support
•Teeth that cannot be restored to function
•Subjects who have taken analgesics within 3 days before treatment commences
•Previous root canal treatment
•Teeth with weeping canals
•Teeth with curved roots
•Teeth with difficulty in determining the working length
•Patients with complications during treatment such as broken files, over-instrumentation, overfilling, or incomplete filling
•Permanent teeth with clinical and radiographical anomalies and anatomical variations

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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