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

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

Tranexamic acid (TXA) is an effective hemostatic agent used to reduce blood loss and the need for transfusion. It is a relatively safe drug with minimal significant side effects. The most commonly reported complications include nausea, diarrhea, and occasional orthostatic reactions. The increased risk of thromboembolic events associated with the drug is the most serious complication; however, this has not been reported in most clinical studies and remains uncertain. Based on experience from other types of surgeries, tranexamic acid appears to be safe for use without an increased risk of venous thrombosis. To mitigate systemic absorption and minimize undesirable side effects, TXA can be applied topically rather than intravenously, reducing the risk of venous thromboembolism.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 14
Maximum Age: 40
Healthy Volunteers: t
View:

• Indicated for the Extraction of Bilaterally Impacted Third Molars with Bone Retention.

• Systemically healthy patients aged 14-40 years with no bleeding disorders.

Locations
Other Locations
Turkey
Bezmialem Vakıf Universty
RECRUITING
Istanbul
Contact Information
Primary
Taha Pergel, Asist.Prof
tahapergel_05@hotmail.com
+902124531850
Time Frame
Start Date: 2025-01-01
Estimated Completion Date: 2026-03-10
Participants
Target number of participants: 20
Treatments
saline irrigation group
In the double-blind, controlled, randomized study, only saline will be used as the irrigation solution in the control group patients.
tranexamic acid Irrigation group
In the double-blind, controlled, randomized study, saline with tranexamic acid solution will be used as the irrigation solution in the study group patients.
Sponsors
Leads: Bezmialem Vakif University

This content was sourced from clinicaltrials.gov

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