Comparison of Postoperative Effects of Articaine and Lidocaine in Mucogingival Surgery (NCT07145879) | Clinical Trial Compass
CompletedNot Applicable
Comparison of Postoperative Effects of Articaine and Lidocaine in Mucogingival Surgery
Turkey (Türkiye)43 participantsStarted 2025-01-01
Plain-language 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 healing, changes in blood flow in the surgical area during the healing process, patients' postoperative pain levels, and anxiety levels before and after surgery.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 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 Criteria:
* 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,
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.