Effectiveness of Intraseptal Anesthesia for Periodontal Surgical Procedures

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
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) in periodontal flap surgery for periodontitis and in gingivectomy/gingivoplasty for the excision of hyperplastic gingival enlargements. The secondary aim is to compare clinical anesthetic parameters between ISA and conventional anesthesia techniques.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• age ≥18 years good systemic health

• gingivitis or periodontitis stage II and III

• at least 20 teeth present.

Locations
Other Locations
Serbia
Department of Periodontology and Oral medicine, School of Dental Medicine, University of Belgrade
RECRUITING
Belgrade
Time Frame
Start Date: 2025-09-22
Estimated Completion Date: 2026-02
Participants
Target number of participants: 60
Treatments
Experimental: GG test
patient subjected to gingivectomy and gingiveplasty interventions and anesthesia of choice is intraseptal anesthesia
Active_comparator: GG control
patient subjected to gingivectomy and gingiveplasty interventions under local infiltration anesthesia
Experimental: PF test
Patients undergoing periodontal flap surgery under intraseptal anesthesia
Active_comparator: PF control
Patients undergoing periodontal flap surgery under local infiltration anesthesia
Related Therapeutic Areas
Sponsors
Leads: University of Belgrade

This content was sourced from clinicaltrials.gov