Pharmacokinetic Study of Tranexamic Acid

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-64
SponsorZhejiang Cancer Hospital

About this trial

Tranexamic acid is an effective anti fibrinolytic drug. Clinical studies have found that intravenous injection of tranexamic acid is more effective in reducing blood loss and transfusion in patients with advanced ovarian cancer, without increasing the risk of postoperative complications. Different surgeries and administration routes have an impact on the pharmacokinetics and pharmacodynamics of TXA. At present, there is little data on the pharmacokinetics of intramuscular injection of TXA, and almost all of the data comes from males. For ovarian cancer patients, there are currently no reports on the pharmacokinetics of TXA through different routes of administration, such as intramuscular and intravenous administration. Therefore, the investigators chose ovarian cancer patients and administered it through different routes of intravenous and intramuscular injection.

Eligibility criteria

Qualifiers

Adult women aged 20-64 diagnosed with advanced ovarian cancer undergoing cytoreductive surgery

The cancer stage is III-IV

ASA classification II-III

Surgical duration>2 hours

Disqualifiers

Renal dysfunction (serum creatinine>200 mmol/L) or liver dysfunction (Child Turcote classification>6)

Has a history of serious mental illness or disorders, epilepsy, visual impairment

Previous or current bleeding disorders, coagulation dysfunction, or thromboembolic events

Lower limb venous thrombosis

Trial design

Treatments tested in this trial

  • Tranexamic acid Intravenous Infusion
  • TXA intramuscular injection

Treatment groups

30 Participants
are divided into 2 treatment groups

Sponsors and collaborators