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Clinical Trials/NCT06725732
NCT06725732RecruitingPhase 1

Assessment of Nebulized Tranexamic Acid in Functional Endoscopic Sinus Surgery Using Modena Bleeding Score. a Randomized Double Blinded Controlled Trial.

Assiut University1 site in 1 country90 target enrollmentStarted: January 29, 2025Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 1
Status
Recruiting
Enrollment
90
Locations
1
Primary Endpoint
Modena Bleeding Score- assessing surgical field

Study Overview

Brief Summary

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.

Detailed Description

Functional endoscopic sinus surgery (FESS) is the current standard treatment for a variety of conditions affecting the nasal cavity and the paranasal sinuses, such as chronic rhinosinusitis, benign and malignant tumors or cerebrospinal fluid leaks .Being mostly a one-handed technique, FESS does not allow simultaneous use of operative instruments and blood suction, thus endonasal bleeding control represents a challenging issue for the operating surgeon. Such narrow and highly vascularized cavities like the nasal fossae and paranasal spaces can be entirely filled with blood within few seconds, especially if the mucosa is severely inflamed as a consequence of rhinosinusitis. Bleeding is possibly the most relevant factor that could impair the quality of the surgical field during endoscopic procedures. It has been proven that uncontrolled bleeding during endoscopic sinus surgical procedures determines poor visualization of the anatomical landmarks, prolongs surgical time and carries a higher rate of complications .Several techniques to control intraoperative bleeding and improve surgical view during sinus surgery (e.g. topical vasoconstrictors, total intravenous anesthesia, controlled hypotension) have been described and analyzed to determine their efficacy .These types of studies, however, are complex and prone to bias, partially because standardized and validated methods of quantifying bleeding or grading the surgical field in endoscopic view are lacking.

Tranexamic acid functions as the competitive antagonist at the lysine site on plasminogen . During all surgical procedures, the tissue plasminogen activator is released due to tissue damage during surgery, which can convert tissue plasminogen to plasmin, promote fibrinolysis and activate the fibrinolytic system. Thus, tranexamic acid functions as an anti-fibrinolytic agent by inhibiting the tissue plasminogen activator. It can be applied topically or systemically with this mechanism in the coagulation cascade to reduce intraoperative bleeding .The results of several recent studies on endoscopic sinus surgery through topical administration of tranexamic acid are encouraging in terms of the efficacy of tranexamic acid for intraoperative bleeding and other pathological conditions .The purpose of this study is to analyze the efficacy of nebulized tranexamic acid and compare it with intravenous tranexamic acid to improve the surgeon and patient experiences of sinus surgery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • 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

Exclusion Criteria

  • • chronic renal failure
  • liver cirrhosis
  • bleeding disorders
  • current anticoagulant therapy
  • pregnancy or breastfeeding
  • impaired color vision
  • severe vascular ischemia
  • history of venous thrombosis, pulmonary embolism
  • long term treatment with acetylsalicylic acid or non-steroidal anti-inflammatory drugs not discontinued before surgery
  • hemoglobin (HB) concentration <10 mg/dl _allergy to TXA.
  • BMI > 35 kg/ m2

Arms & Interventions

Intravenous

Experimental

Intervention: Tranexamic Acid (Drug)

Nebulized

Experimental

Intervention: Tranexamic Acid (TXA) (Drug)

Outcomes

Primary Outcomes

Modena Bleeding Score- assessing surgical field

Time Frame: Baseline

* No bleeding -\>1. * Bleeding easily controlled by suctioning, washing, or packing without any significant modification or slowing of surgical procedure-\>2. * Bleeding slowing surgical procedure-\>3. * Most of the maneuvers dedicated to bleeding control -\>4. * Bleeding that prevents every surgical procedure except those dedicated to bleeding control-\>5.

Secondary Outcomes

  • Measuring patient's Blood Pressure-> mmhg (unit of measure)(Baseline)
  • Measuring patient's Respiratory Rate-> breath per minute(unit of measure)(Baseline)
  • Measuring patient's Temperature-> Celsius(unit of measure)(Baseline)
  • Measuring patient's Pulse->Beat per minute(unit of measure)(Baseline)
  • Measuring End-tidal Co2 by Capnogram(Baseline)
  • Measuring O2 saturation by the pulse-oximeter(Baseline)
  • Measuring amount of intraoperative bleeding through blood volume in suction jar(Baseline)
  • Measuring the amount of intraoperative bleeding by counting gauze used in the operation.(Baseline)
  • 2. Anesthetic consumption, Extra doses of fentanyl and propofol and sevoflurane>2(Baseline)
  • Presence or absence of nausea as a Postoperative complication(Baseline)
  • Presence or absence of vomiting as a Postoperative complication(Baseline)
  • Presence or absence of any form of visual disturbance as a Postoperative complication(Baseline)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Asmaa Zanaty

Assistant Lecturer

Assiut University

Study Sites (1)

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