CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 1,089 enrolled
Drug / intervention
Tranexamic Acid 100 MG/ML +1 moredrug
Likely dose
Tranexamic Acid 100 MG/MLfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03690037
NCT03690037Phase 4Completed

Single Centre Randomised Controlled Trial to Assess the Effect of the Addition of Twenty-four Hours of Oral Tranexamic Acid Post-operatively to a Single Intra-operative Intravenous Dose of Tranexamic Acid on Calculated Blood Loss Following Primary Hip and Knee Arthroplasty.

Belfast Health and Social Care Trust·interventional·Posted Oct 1, 2018·Updated Apr 15, 2022

In Brief

A Phase 4 clinical trial evaluating Tranexamic Acid 100 MG/ML and Tranexamic Acid 500 MG for Primary Total Knee Arthroplasty and Primary Total Hip Arthroplasty. Completed, enrolled 1,089 participants across 1 site.

Detailed Summary

Patients having a hip or knee replacement can lose almost a third of their blood during and after the operation. Many patients, especially those who are older will need a blood transfusion, suffer from anaemia, or have a slow recovery after the operation. Tranexamic acid is a medication used to treat or prevent excessive blood loss, but in joint replacements, is only used in patients who are likely to bleed a lot. This trial aims to find out how well tranexamic acid works to reduce blood loss after the operation in a large group of patients having a hip or knee replacement, including those at risk of blood clots. This study also aims to find out how safe tranexamic acid treatment is to use in different patients and the best way to give tranexamic acid (in tablet form or through a drip), as well as how much to give and how long it should be given after an operation. All adults awaiting non-emergency hip or knee replacement surgery will be considered. Patients who are suitable and agree to take part are randomly placed in one of two treatment groups: receiving tranexamic acid during the hip or knee operation through a drip, or receiving treatment during the hip or knee operation through a drip plus taking a tablet every 8 hours up to 24 hours after the operation. Initially, a no treatment group was included, however, one year after the trial started, the Data Monitoring and Ethics Committee who check safety, advised to stop allocation of patients to the no treatment group. For all patients, blood loss is recorded up to 48 hours after surgery. Blood samples are also taken in order to measure how well the heart and blood clotting systems are working. If the routine kidney function tests taken before the operation show less than normal function, a lower dose of tranexamic acid is used. It is expected that patients who receive the tranexamic acid will lose much less blood during and after their operation, and so be less likely to need a blood transfusion, have reduced stress on the heart and have an easier recovery. It is thought that patients with a history of clots are more likely to have another clot when taking tranexamic acid. Therefore, this trial will include these patients to try and find out if this is true as these patients will benefit the most from reduced blood loss.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited Kingdom
Collaborators--

Timeline

Phase 4CompletedFinished
2017201820192020202120222023202420252026
First PostedOct 1, 2018
Enrollment StartJul 7, 2016
Primary CompletionJul 8, 2018
Study CompletionJul 8, 2019
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 7.8 years ago

Interventions

Tranexamic Acid 100 MG/MLdrug

Tranexamic Acid: 100 MG/ML Solution for injection

Tranexamic Acid 500 MGdrug

Tranexamic Acid: Tranexamic Acid 500mg Tablets