Actively Recruiting

Age: 14Years - 40Years
All Genders
Healthy Volunteers
ID06806241

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

Age: 14Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

Loading map...

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

Similar Trials

Anticoagulation for New-Onset Post-Operative Atrial Fibrilla...

Atrial Fibrillation

Actively Recruiting

101 locations

Assessing Levels of Fear and Anxiety and Monitoring Wound He...

Tooth Extraction

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here