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RecruitingNCT05047133

Effect of Early Administration of TXA in Adult Hip Fractures

Does Early Administration of Tranexamic Acid Decrease Perioperative Blood Loss in Addition to Intraoperative Tranexamic Acid for Hip Fracture Patients?

Status
Recruiting
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
170 (estimated)
Sponsor
Ascension Health · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This is a prospective clinical study designed to assess blood loss in intracapsular and extracapsular hip fractures undergoing operative fixation at a Level II trauma center. It is well established in the orthopedic literature that tranexamic acid (TXA) decreases blood loss and need for postoperative blood transfusion in hip fracture patients as well as total joint arthroplasty patients. A typical dosing pattern, and the dosing pattern employed at our institution, is 1 gram IV infused prior to incision followed by 1 gram IV infused at the time of wound closure.

Conditions

Interventions

TypeNameDescription
DRUGTranexamic acidTXA to be given at time of diagnosis in the emergency department (ED) in treatment group and at time of operation for both groups

Timeline

Start date
2021-09-01
Primary completion
2022-07-01
Completion
2022-07-01
First posted
2021-09-16
Last updated
2021-09-16

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05047133. Inclusion in this directory is not an endorsement.

Effect of Early Administration of TXA in Adult Hip Fractures (NCT05047133) · Clinical Trials Directory