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Recruiting NCT07212270

NCT07212270 Effectiveness of Intraseptal Anesthesia for Periodontal Surgical Procedures

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Clinical Trial Summary
NCT ID NCT07212270
Status Recruiting
Phase
Sponsor University of Belgrade
Condition Periodontitis
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2025-09-22
Primary Completion 2026-03

Trial Parameters

Condition Periodontitis
Sponsor University of Belgrade
Study Type INTERVENTIONAL
Phase N/A
Enrollment 60
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-09-22
Completion 2026-03
Interventions
periodontal flap surgerygingivectomy and gingivoplasty

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Brief Summary

The primary aim of this study is to evaluate the efficacy of intraseptal anesthesia using 0.3 mL of 4% articaine with 1:100,000 epinephrine (4% Ar+Ep) for periodontal flap surgery in patients with periodontitis and for gingivectomy/ gingivoplasty for the excision of hyperplastic gingival enlargements. The secondary aim is to compare clinical anesthetic parameters between the ISA and conventional anesthesia techniques.

Eligibility Criteria

Inclusion Criteria: * age ≥18 years good systemic health * gingivitis or periodontitis stage II and III * at least 20 teeth present. Exclusion Criteria: * allergy to 4%Ar+Ep * pregnant or lactating females * medication uptake and diseases affecting the periodontal tissues * acute pain, swelling, and presence of gingival lesions.

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