Tranexamic Acid in Rhinoplasty: Perioperative Bleeding, Edema and Ecchymosis

Sponsor
Vanderbilt University Medical Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05774717
Collaborator
(none)
60
1
2
10.1
6

Study Details

Study Description

Brief Summary

This study will be a prospective randomized study to evaluate the effect of tranexamic acid (TXA) use on intraoperative and postoperative outcomes among patients undergoing rhinoplasty by two Facial Plastic surgeons at Vanderbilt. Outcomes will include intra- and post-operative bleeding and postoperative bruising and swelling.

Condition or Disease Intervention/Treatment Phase
  • Drug: Tranexamic acid
Phase 1

Detailed Description

TXA is an antifibrinolytic agent that acts to decrease bleeding by stabilizing the fibrin matrix involved in the clotting cascade. The use of TXA, oral or intravenous, has been extensively used and described in the literature to prevent exsanguination in trauma and in various surgical procedures, as well as for heavy menstrual bleeding. It has been used in the perioperative period during various nasal and sinus surgery, and current research in rhinoplasty suggests that its use may decrease intraoperative bleeding and postoperative eye swelling and bruising.

Currently, IV TXA is used at this institution in some cases by some surgeons in the perioperative period in rhinoplasty surgery, though its used is not standardized and has not been studied. This study will randomize patients undergoing rhinoplasty, with consent, to receive TXA or placebo in the perioperative period. The investigators anticipate collecting 60-100 patients. Outcomes will include intraoperative bleeding, postoperative swelling and bruising (both subjective and based on blinded reviewer analysis of postoperative photographs).

TXA has been used in the perioperative period during various nasal and sinus surgery, and current research in rhinoplasty suggests that its use may decrease intraoperative bleeding and postoperative eye swelling and bruising. In these studies, TXA has been given in intravenous and/or oral form in 1-3 doses in the perioperative period, and there have been no serious adverse effects reported. IV TXA is also FDA approved for use at time of tooth extraction to decrease bleeding, and PO TXA is approved use during the menstrual cycle to decrease heavy menstrual bleeding. There are countless studies in the literature supporting use of both IV and PO TXA in trauma, orthopedic and spine surgery and neurosurgery, and it is widely used in clinical practice in these disciplines. It's use in rhinoplasty is growing, yet has not been studied in larger groups.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
One group receives tranexamic acid prior to surgery, one group receives nothing (routine care).One group receives tranexamic acid prior to surgery, one group receives nothing (routine care).
Masking:
None (Open Label)
Masking Description:
Provider will order tranexamic acid based based on even versus odd last digit of medical record number (MRN). Patient will be blinded, as will all personnel analyzing postoperative photographs and other data.
Primary Purpose:
Prevention
Official Title:
Tranexamic Acid in Rhinoplasty: Perioperative Bleeding, Edema and Ecchymosis
Anticipated Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Feb 1, 2024
Anticipated Study Completion Date :
Feb 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Tranexamic Acid

Patients receive 1 gram IV tranexamic acid in the operating room prior to surgical incision.

Drug: Tranexamic acid
1 gram IV (intravenous) tranexamic acid administered in the operating room just prior to starting the case (10 minutes), at time that routine preoperative antibiotic is given.
Other Names:
  • TXA
  • No Intervention: Control

    Routine care, no tranexamic acid given.

    Outcome Measures

    Primary Outcome Measures

    1. Intraoperative bleeding as measured by the weight of surgical sponges used [During surgery]

      Weight of surgical sponges used (grams)

    2. Intraoperative bleeding as measured by the volume of blood in suction canister [Intraoperative]

      Volume of blood in suction canister (Milliliters)

    3. Postoperative bleeding as measured by patient-rated bleeding on Visual Analog Scale (VAS) [Up to one week following surgery.]

      A single patient-answered question visual analog scale (VAS) used to measure the amount of post-operative bleeding from the nose the participant experienced (1 to 5 scale with 5 being the most)

    4. Postoperative edema [Up to one week following surgery]

      Swelling around the eyes (Visual Analog Scale, 1 to 5 scale with 5 being the most)

    5. Postoperative ecchymosis [Up to one week following surgery]

      Bruising around the eyes (Visual Analog Scale, 1 to 5 scale with 5 being the most)

    6. Postoperative bleeding as measured by the number of medical interventions needed to control bleeding [Up to one week following surgery]

      Number of interventions required to control bleeding (surgical or procedural interventions)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Adults at least 18 years of age who elect to undergo cosmetic or functional open primary rhinoplasty with osteotomies (repositioning the nasal bones) by Drs. Yang or Patel at VUMC.

    • No other facial plastics procedure nor sinus surgery performed simultaneously

    • Lack all the below Exclusion Criteria

    Exclusion Criteria:
    • Known allergy to TXA (tranexamic acid)

    • Intracranial bleeding

    • Known defective color vision

    • History of venous or arterial thromboembolism

    • Active thromboembolic disease

    • Severe renal impairment (diagnosis of chronic kidney disease)

    • History of coagulation disorder

    • Known thrombocytopenia (platelets <150,000)

    • Current use of anticoagulant (blood thinner)

    • Uncontrolled DM (diabetes mellitus) preventing use of dexamethasone in the perioperative period

    • Cardiac arrhythmia

    • History of AMI (acute myocardial infarction), stroke, seizure, liver failure

    • Laboratory results showing platelets <150,000, PT (prothrombin time) >45, INR (international normalized ratio) >1.2, seizure disorder

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Vanderbilt University Medical Center Nashville Tennessee United States 37232

    Sponsors and Collaborators

    • Vanderbilt University Medical Center

    Investigators

    • Principal Investigator: Shiayin F Yang, MD, Vanderbilt University Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Shiayin Yang, Assistant Professor of Otolaryngology, Vanderbilt University Medical Center
    ClinicalTrials.gov Identifier:
    NCT05774717
    Other Study ID Numbers:
    • 221035
    First Posted:
    Mar 20, 2023
    Last Update Posted:
    Mar 20, 2023
    Last Verified:
    Mar 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 20, 2023