Assessment of Nebulized Tranexamic Acid in Functional Endoscopic Sinus Surgery Using Modena Bleeding Score

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAssiut University

About this trial

The aim of this study is to investigate the effect of preoperative administration of intravenous or nebulized tranexamic acid on surgical field, blood loss, anesthetic consumption and hemodynamics of patients undergoing FESS.

Primary outcome Modena Bleeding Score (MBS) assessing surgical field Secondary outcome

1. Patient hemodynamics. 2. Anesthetic consumption, Extra doses of fentanyl and propofol and sevoflurane\>2 3. Postoperative complications: including any adverse effects to TXA e.g.nausea, vomiting, any visual disturbances, fits, and any thrombotic manifestation.

Eligibility criteria

Qualifiers

Either sex

age 18-65 years

ASA I-II who are listed for elective functional endoscopic sinus surgery (FESS) under general anesthesia

normal accepted coagulation profile and hematocrit value ≥30

Disqualifiers

• chronic renal failure

liver cirrhosis

bleeding disorders

current anticoagulant therapy

Trial design

Treatments tested in this trial

  • Tranexamic Acid (TXA)
  • Tranexamic Acid

Treatment groups

90 Participants
are divided into 2 treatment groups

Sponsors and collaborators