Status:
COMPLETED
Comparison of Postoperative Effects of Articaine and Lidocaine in Mucogingival Surgery
Lead Sponsor:
Pamukkale University
Conditions:
Local Analgesia Via Infiltration
Wound Heal
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The aim of this study is to compare and evaluate the effects of using lidocaine 2% (with adrenaline) and articaine 4% (with adrenaline) in free gingival graft (FGG) surgery on postoperative wound heal...
Detailed Description
In a prospective randomised controlled trial conducted to investigate the effect of lidocaine and articaine on postoperative free gingival graft healing, wound healing was assessed using EHS, anxiety ...
Eligibility Criteria
Inclusion
- Patients\> 18 years requiring FGG surgery with ≤ 1 mm width of attached gingiva
- No systemic diseases or pregnancy.
- Smoking ≤10 cigarettes/day
- Full-mouth plaque score and full-mouth bleeding score ≤10% (four sites per tooth).
- Need for FGG due to insufficient attached gingiva
- No history of mucogingival or periodontal surgery at experimental sites
Exclusion
- Use of oral contraceptives, psychotropic drugs, sedatives, or NSAIDs
- Allergy or hypersensitivity to local anesthetics,
- Orofacial neurological symptoms,
- Active infection in the surgical area,
- Pathological mental conditions such as dementia or psychosis, or lack of cooperation,
Key Trial Info
Start Date :
January 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 30 2025
Estimated Enrollment :
43 Patients enrolled
Trial Details
Trial ID
NCT07145879
Start Date
January 1 2025
End Date
July 30 2025
Last Update
August 28 2025
Active Locations (1)
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1
Pamukkale University Faculty of Dentistry
Denizli, Turkey (Türkiye), 20100