Can the Prophylactic Administration of Tranexamic Acid Reduce Blood Loss After Robotic-assisted Radical Prostatectomy? (RARPEX)
Primary Purpose
Robotic-assisted Radical Prostatectomy
Status
Completed
Phase
Phase 4
Locations
Czechia
Study Type
Interventional
Intervention
Tranexamic Acid Injectable Product
Placebos
Sponsored by

About this trial
This is an interventional prevention trial for Robotic-assisted Radical Prostatectomy focused on measuring Tranexamic acid, robotic assisted radical prostatectomy, bleeding prophylaxis
Eligibility Criteria
Inclusion Criteria:
- Patients scheduled for robotic-assisted radical prostatectomy without pelvic lymph node dissection
- Signed informed consent provided
- Body mass index ≤ 35
- Age of the patient ≤ 75 years
- Operating surgeon with experience > 100 cases
Exclusion Criteria:
- Body mass index > 35
- Age of the patient > 75 years
- Coagulation disorder (congenital or iatrogenic due to the chronic use of anticoagulants)
- Thromboembolic, cerebral, or an acute coronary event within the 6 months prior to prostatectomy
- Chronic renal insufficiency (arbitrary cut-off level of creatinine 200 μmol/l)
- Allergic reaction to tranexamic acid
- Operating surgeon with experience < 100 cases
- Participation in other study
Sites / Locations
- University Hospital Hradec Králové
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Tranexamic acid
Saline
Arm Description
Outcomes
Primary Outcome Measures
Reduction of blood loss
The drop of hemoglobin level, weighted on gram of prostate or creatinin level.
Secondary Outcome Measures
The risk of postoperative complications
The incidence and severity of postoperative complications according to Dindo/Clavien Classification.
Full Information
NCT ID
NCT04319614
First Posted
March 20, 2020
Last Updated
November 6, 2022
Sponsor
University Hospital Hradec Kralove
1. Study Identification
Unique Protocol Identification Number
NCT04319614
Brief Title
Can the Prophylactic Administration of Tranexamic Acid Reduce Blood Loss After Robotic-assisted Radical Prostatectomy?
Acronym
RARPEX
Official Title
Can the Prophylactic Administration of Tranexamic Acid Reduce Blood Loss After Robotic-assisted Radical Prostatectomy? The RARPEX (Robotic Assisted Radical Prostatectomy With TranEXamic Acid) Study.
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
February 24, 2020 (Actual)
Primary Completion Date
February 12, 2022 (Actual)
Study Completion Date
June 30, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Hradec Kralove
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The prophylactic administration of tranexamic acid reduces blood loss during procedures at high risk of perioperative bleeding. Several studies in neurosurgery, cardiac surgery, and orthopedics confirm this finding. The aim of this study is to evaluate the effect of tranexamic acid on peri-and postoperative blood loss and incidence and severity of postoperative complications. A prospective, double-blind, randomized study is conducted to evaluate the effect on several parameters.
Based on pilot study data the investigators decided to include 200 patients in the period from February 2020 to March 2022. The patients will be randomly assigned to study and control groups of 100 patients each. The minimum follow-up will be 3 months.
Detailed Description
Prostate adenocarcinoma is the second most common malignancy and the second most common cause of death due to malignancy in men. Standard treatment includes radical prostatectomy or radiotherapy in patients with life expectancy for more than 10 years. In recent years, a general tendency toward minimally invasive surgical procedures has been seen. Despite tremendous development in the technology and technique of robotic-assisted radical prostatectomy for more than 25 years, there is still need to look for ways to improve oncological and functional outcomes. Decreasing peri- and postoperative blood loss may lead to faster recovery after the procedure.
Tranexamic acid is an antifibrinolytic used to relieve bleeding. The mechanism of action lies in binding to plasma free plasminogen with higher affinity than tissue plasminogen activator. It prevents its conversion to plasmin, which is responsible for the degradation of fibrin polymers. It results in greater stability of the fibrin clot at the site of bleeding and, therefore, lower blood loss. The use of tranexamic acid during or after the operation does not improve results, unlike administration prior to surgery and the dorsal complex vein is sutured in the beginning of the procedure.
This study is designed to answer the question of whether it might lower the drop in hemoglobin level after the procedure or increase the rate and severity of complications.
This trial was approved by the independent ethics committee at the University Hospital Hradec Kralove (registration number 201903 I90P).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Robotic-assisted Radical Prostatectomy
Keywords
Tranexamic acid, robotic assisted radical prostatectomy, bleeding prophylaxis
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Tranexamic acid
Arm Type
Experimental
Arm Title
Saline
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Tranexamic Acid Injectable Product
Intervention Description
A single dose of tranexamic acid, corresponding to 20 mg/kg in 100 ml saline, will be administered in the beginning of procedure.
Intervention Type
Drug
Intervention Name(s)
Placebos
Intervention Description
100 ml of saline will be administered in the beginning of the procedure.
Primary Outcome Measure Information:
Title
Reduction of blood loss
Description
The drop of hemoglobin level, weighted on gram of prostate or creatinin level.
Time Frame
7 days after the procedure
Secondary Outcome Measure Information:
Title
The risk of postoperative complications
Description
The incidence and severity of postoperative complications according to Dindo/Clavien Classification.
Time Frame
90 days after the procedure
10. Eligibility
Sex
Male
Gender Based
Yes
Gender Eligibility Description
Patients with prostate cancer
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients scheduled for robotic-assisted radical prostatectomy without pelvic lymph node dissection
Signed informed consent provided
Body mass index ≤ 35
Age of the patient ≤ 75 years
Operating surgeon with experience > 100 cases
Exclusion Criteria:
Body mass index > 35
Age of the patient > 75 years
Coagulation disorder (congenital or iatrogenic due to the chronic use of anticoagulants)
Thromboembolic, cerebral, or an acute coronary event within the 6 months prior to prostatectomy
Chronic renal insufficiency (arbitrary cut-off level of creatinine 200 μmol/l)
Allergic reaction to tranexamic acid
Operating surgeon with experience < 100 cases
Participation in other study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Milos Brodak, Prof.MD, PhD.
Organizational Affiliation
University Hospital Hradec Kralove
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Michal Balik, MD
Organizational Affiliation
University Hospital Hradec Kralove
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Hradec Králové
City
Hradec Králové
ZIP/Postal Code
50005
Country
Czechia
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
33355078
Citation
Balik M, Kosina J, Husek P, Brodak M, Cecka F. Safety and Efficacy of Using Tranexamic Acid at the Beginning of Robotic-Assisted Radical Prostatectomy in a Double-Blind Prospective Randomized Pilot Study. Acta Medica (Hradec Kralove). 2020;63(4):176-182. doi: 10.14712/18059694.2020.60.
Results Reference
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PubMed Identifier
35717263
Citation
Balik M, Kosina J, Husek P, Pacovsky J, Brodak M, Cecka F. Can the prophylactic administration of tranexamic acid reduce the blood loss after robotic-assisted radical prostatectomy? Robotic Assisted Radical Prostatectomy with tranEXamic acid (RARPEX): study protocol for a randomized controlled trial. Trials. 2022 Jun 18;23(1):508. doi: 10.1186/s13063-022-06447-x.
Results Reference
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