Skip to main content
OpenTrials
Completed

NCT Number: NCT06086444

Tranexamic Acid in Abdominoplasty.

The investigators prepared a novel tranexamic acid (TXA) study designed to estimate the quantity of blood loss in patients undergoing abdominoplasty surgery. This study aims to quantify blood loss during abdominoplasty with and without TXA. The central hypothesis is that TXA administration reduces blood loss and fibrinolysis in patients undergoing abdominoplasty surgery.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Poznan University of Medical Sciences

Poznan, Poznań, 61-701, Poland

About this study

Tranexamic acid (TXA) treatment is increasingly emphasized in plastic surgery because TXA inhibits fibrinolysis. Increased clot stability offers the possibility of preventing blood loss (prevention) and mitigating ongoing hemorrhage. TXA therapy has been principally studied in populations; the results of studies in plastic surgery still need to be improved.

Tranexamic acid is an antifibrinolytic agent that acts as a competitive inhibitor at the lysine binding sites of plasminogen and inhibits the ability of protease plasmin to cleave the fibrin clot. In large randomized controlled trials, it has been reported to be effective in decreasing perioperative blood loss in various circumstances, primarily involving trauma patients.

The investigators designed a randomized placebo-controlled trial comparing TXA dosing before incision for abdominoplasty. The purpose is to quantify blood loss during plastic surgery with and without TXA.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Scheduled abdominoplasty
  • ASA 1 or 2
  • age >18 and <75 years

Exclusion criteria

  • BMI <20 or >35 kg/m2
  • ASA 3 or > 3
  • medical history of thromboembolism
  • history of hematological disease
  • treatment with aspirin 14 days before the procedure
  • treatment with anticoagulants 5 days before the procedure
  • epilepsy
  • allergy to tranexamic acid
  • coagulation disorders

Treatment and study plan

Placebo

Drug

100 mL of normal saline. Administered intravenously at least 10 minutes prior to skin incision.

Other names: 0.9% sodium chloride

Tranexamic Acid

Drug

Tranexamic Acid (10mg/kg), diluted in 100 ccs of normal saline. Administered intravenously at least 10 minutes before skin incision.

Other names: TXA

Primary outcomes

  1. Blood loss volume

    Time frame: 24 hours after surgery

    Total blood volume loss will be calculated in milliliters.

Secondary outcomes

  1. HBG

    Time frame: 24 hours after surgery

    Hemoglobin level measured before and 24 hours after surgery

  2. D-dimer

    Time frame: 24 hours after surgery

    D-dimer level measured before and 24 hours after surgery

  3. Fibrinogen

    Time frame: 24 hours after surgery

    Fibrinogen level measured before and 24 hours after surgery

Sponsors and collaborators

Lead sponsor

Poznan University of Medical Sciences

Other

Registry information

Official study title

The Effectiveness of Tranexamic Acid in Abdominoplasty Plastic Surgery.

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Oct 17, 2023
Registry last updated
Nov 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.