Actively Recruiting

Phase 4
Age: 19Years +
FEMALE
Healthy Volunteers
NCT06356948

Rate of Tranexamic Acid Administration on Blood Pressure (RateTXA) Study.

Led by University of British Columbia · Updated on 2024-04-10

110

Participants Needed

1

Research Sites

195 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Tranexamic acid is a well-established treatment for post-partum hemorrhage. This study aims to examine the effect of tranexamic acid administration rates on blood pressure changes over 1 minute compared to 10 minutes in healthy pregnant patients scheduled for cesarean delivery.

CONDITIONS

Official Title

Rate of Tranexamic Acid Administration on Blood Pressure (RateTXA) Study.

Who Can Participate

Age: 19Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant patients at 34 weeks gestation or more scheduled for elective cesarean delivery under single-shot spinal anesthesia
  • American Society of Anesthesiologists (ASA) Physical Status Class 2
  • Patients 19 years of age or older
Not Eligible

You will not qualify if you...

  • Known history of pre-existing hypertension or pregnancy-related hypertension disorders
  • Recent use of medications to treat high blood pressure (e.g., labetolol, hydralazine, nifedipine)
  • Recent use of medications that can affect blood pressure, including beta blockers for anxiety or sedative pre-medications (e.g., propranolol, midazolam, lorazepam)
  • Known allergy or sensitivity to tranexamic acid or related drugs
  • Elective cesarean requiring general anesthesia or neuraxial methods other than single-shot spinal anesthesia
  • Inability to give informed consent due to language barriers
  • Arriving late to surgical day care with less than 90 minutes before scheduled cesarean delivery time

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

BC Women's Hospital

Vancouver, British Columbia, Canada, V6H3N1

Actively Recruiting

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Research Team

A

Aislynn Sharrock, BSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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