Actively Recruiting
Investigation of the Effects of Tranexamic Acid Solution Irrigation on Bleeding, Surgical Field Visibility, and Postoperative Edema in the Extraction of Horizontally Impacted Third Molars
Led by Bezmialem Vakif University · Updated on 2025-06-24
20
Participants Needed
1
Research Sites
1 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the use of tranexamic acid (TXA) irrigation during the extraction of horizontally impacted third molars to reduce bleeding, improve surgical field visibility, and lessen postoperative swelling (edema). TXA is known as a hemostatic agent that reduces blood loss and the need for transfusions, with minimal significant side effects. The study aims to explore the effect of topical TXA irrigation during tooth extraction under local anesthesia, which has not been previously reported. The study compares two groups in a double-blind, controlled, randomized design. One group will receive saline irrigation during surgery, while the other group will have saline mixed with tranexamic acid as the irrigation solution. The topical application is intended to minimize systemic absorption and reduce risks such as venous thromboembolism. Researchers will monitor intraoperative bleeding, surgical field visibility, and postoperative edema in both groups. Participants will undergo extraction of bone-retained impacted third molars while researchers assess bleeding and visibility during surgery and measure swelling three days after surgery. The study includes patients aged 14 to 40 years who are systemically healthy and free from bleeding disorders. Monitoring will focus on surgical conditions and postoperative recovery, with the main outcome being edema three days after surgery. Total participation spans the surgical procedure and follow-up assessments shortly thereafter.
CONDITIONS
Brief Title
Effects of Tranexamic Acid Irrigation on Impacted Third Molar Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Indicated for the Extraction of Bilaterally Impacted Third Molars with Bone Retention
- Systemically healthy patients aged 14 to 40 years
- No bleeding disorders
You will not qualify if you...
- Patients with systemic diseases affecting general health
- Patients diagnosed with any bleeding disorder
- Patients with advanced infection or cysts associated with the impacted tooth
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Surgery day plus 3 days of postoperative monitoring
Participants undergo extraction of impacted third molars with irrigation using either tranexamic acid solution or saline to monitor bleeding, surgical field visibility, and postoperative swelling.
1 surgery visit and 1 follow-up visit within 3 days post-surgery
Trial Site Locations
Total: 1 location
1
Bezmialem Vakıf Universty
Istanbul, Fatih, Turkey (Türkiye), 34093
Actively Recruiting
Research Team
T
Taha Pergel, Asist.Prof
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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