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The Plasma Large-Volume Exchange RCT (PLEX-RCT)

Primary Purpose

Purpura, Thrombotic Thrombocytopenic, Hemolytic Uremic Syndrome

Status
Withdrawn
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Plasma Exchange
Sponsored by
London Health Sciences Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Purpura, Thrombotic Thrombocytopenic focused on measuring Thrombotic thrombocytopenia purpura, hemolytic uremic syndrome, plasma exchange, Improve treatment response, TTP/HUS

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age > 18 year-old
  2. First presentation of TTP/HUS
  3. Meet all of the following diagnostic criteria:

    • Platelet count < 150 x 109 /L
    • Microangiopathic haemolytic anaemia (blood film with presence of red blood cell fragmentation)
    • LDH > 1.25 X the upper limits of normal
    • No alternative diagnosis

Exclusion Criteria:

  1. Secondary TTP/HUS
  2. Relapsing TTP/HUS
  3. Hypersensitivity to blood product
  4. Patient has received 2 or more plasma exchange treatment since symptom started over the last 1 week
  5. Received medication, including cyclosporine, cyclophosphamide, rituximab for treatment of TTP/HUS
  6. Other causes of thrombocytopenia than TTP/HUS

Sites / Locations

  • Central Facility

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard-dose plasma exchange

High-dose Plasma Exchange

Arm Description

50-75 ml/kg/day

125 ml/kg/day up to 10 L/day

Outcomes

Primary Outcome Measures

treatment failure at day 5 and/or 2) non-response or death at 2 weeks
LDH >1.25 x the upper limit of normal at Day 5 and <50% decrease from initial value, or Initial platelet count <50 x 109/L with <100% rise at Day 5, or Initial platelet count 50-99 x 109/L with <50% rise at Day 5, or Initial platelet count 100-150 x 109/L with Day 5 <150x 109/L, or LDH >1.25 x the upper limit of normal at 2 weeks, or Platelet count <150 x 109/L at 2 weeks, or Persistent or new neurological symptoms at 2 weeks

Secondary Outcome Measures

All-cause mortality
all-cause mortality at 1-month and 6-months after treatment initiation

Full Information

First Posted
September 9, 2011
Last Updated
April 16, 2013
Sponsor
London Health Sciences Centre
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1. Study Identification

Unique Protocol Identification Number
NCT01433003
Brief Title
The Plasma Large-Volume Exchange RCT
Acronym
PLEX-RCT
Official Title
The Plasma Large-Volume Exchange Randomized Controlled Trial (PLEX-RCT)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Withdrawn
Why Stopped
Funding not obtained
Study Start Date
April 2012 (undefined)
Primary Completion Date
December 2014 (Anticipated)
Study Completion Date
March 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
London Health Sciences Centre

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Thrombotic thrombocytopenia purpura / hemolytic uremic syndrome (TTP/HUS) is a rare, life-threatening disorder. TTP/HUS causes multiple blood clots to form, which prevents blood from reaching the brain and kidneys. TTP/HUS affects 3-5 people per million per year. Anyone can develop TTP/HUS, but it is most common among 30-40 year olds, and women are twice as likely as men to acquire the condition. TTP/HUS sometimes develops as a result of medication use, pregnancy or cancer; however, for the majority of patients (80%) the cause of TTP/HUS is unknown. In 1991, researchers discovered that plasma exchange was superior to plasma infusion in treating idiopathic TTP/HUS. During plasma exchange the patient's blood plasma is removed and replaced with healthy blood plasma. Without plasma exchange, the survival rate for TTP/HUS is extremely low, with fewer than 5% of patients surviving. Treating TTP/HUS with plasma exchange improved the survival rate to 80%. Although this represents a dramatic improvement, researchers are still searching for methods to improve survival. No major advances in treating TTP/HUS have occurred in the past 20 years. Recent research suggests that high-dose plasma exchange may improve the survival of TTP/HUS patients. The investigators will conduct a randomized controlled trial to test whether treating TTP/HUS patients with high-dose versus standard-dose plasma exchange improves the treatment response. The investigators will recruit 150 patients with TTP/HUS from 9 centres across Canada over three years. The investigators will evaluate whether high-dose plasma exchange improves the treatment response, survival, and whether it reduces the number and volume of plasma exchange procedures and duration of hospital stay.
Detailed Description
Background: Thrombotic thrombocytopenia purpura / haemolytic uremic syndrome (TTP/HUS) is a rare blood disorder with a high mortality rate of >95% when left untreated. In 1991, researchers discovered that treating TTP/HUS with plasma exchange vs. plasma infusion dramatically improved the survival rate, from 60% to 80%.The optimal plasma dose for treating TTP/HUS is unknown; however, recent research suggests that high-dose plasma exchange may improve survival in patients with TTP/HUS. Hypothesis: Treatment of TTP/HUS with high-dose vs. standard-dose plasma exchange will significantly decrease the composite outcome of 1) treatment failure at day 5 and/or 2) non-response or death at 2 weeks. Methods: The investigators will conduct a multi-centre, parallel group randomized controlled trial. The investigators anticipate recruiting 150 eligible patients with idiopathic TTP/HUS from 9 centres across Canada over 2.25 years. Patients will be randomized to receive high-dose plasma exchange (125 ml/kg/day up to 10 L/day plasma volume) or standard-dose plasma exchange (50-75 ml/kg/day; approximately 1-1.5 plasma volume). The primary composite outcome includes treatment failure at day 5 or non-response or death from any cause at 2 weeks. Secondary outcomes include the individual components of the primary outcome, non-response or death from any cause at month 1 and month 6, days to remission, duration of hospital stay, number and volume of plasma exchange treatments, and cost minimization. Research Team: Our multi-centre team is part of the Canadian Apheresis Group, which was established in 1980 and currently operates in 30 centres across Canada. Collectively, the Canadian Apheresis Group treats 150 TTP/HUS patients each year. Our team includes experienced haematologists, nephrologists, epidemiologists and a biostatistician. The investigators have successfully collaborated on several projects and have an excellent publication record (>50 publications across more than 15 journals including the New England Journal of Medicine). Timeline and Budget: Because TTP/HUS is a relatively rare disorder (an orphan disease), the investigators will recruit patients over 2.25 years from across Canada to achieve a sufficiently large sample size. A cost minimization study will be carried out in conjunction with the RCT to provide insight into potential costing. Future Directions: If the investigators can demonstrate that high-dose plasma exchange significantly improves the primary outcome, the investigators will pursue a multi-national collaboration with American, Chinese and European Centres to investigate other important outcomes including optimal dosing, cost-effectiveness and survival. Implications: This study has the potential to be the first major advancement in treating TTP/HUS in twenty years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Purpura, Thrombotic Thrombocytopenic, Hemolytic Uremic Syndrome
Keywords
Thrombotic thrombocytopenia purpura, hemolytic uremic syndrome, plasma exchange, Improve treatment response, TTP/HUS

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard-dose plasma exchange
Arm Type
Active Comparator
Arm Description
50-75 ml/kg/day
Arm Title
High-dose Plasma Exchange
Arm Type
Experimental
Arm Description
125 ml/kg/day up to 10 L/day
Intervention Type
Procedure
Intervention Name(s)
Plasma Exchange
Intervention Description
Plasma exchange is a blood purification technique that removes plasma from the blood and replaces it with donor plasma.
Primary Outcome Measure Information:
Title
treatment failure at day 5 and/or 2) non-response or death at 2 weeks
Description
LDH >1.25 x the upper limit of normal at Day 5 and <50% decrease from initial value, or Initial platelet count <50 x 109/L with <100% rise at Day 5, or Initial platelet count 50-99 x 109/L with <50% rise at Day 5, or Initial platelet count 100-150 x 109/L with Day 5 <150x 109/L, or LDH >1.25 x the upper limit of normal at 2 weeks, or Platelet count <150 x 109/L at 2 weeks, or Persistent or new neurological symptoms at 2 weeks
Time Frame
baseline to two weeks
Secondary Outcome Measure Information:
Title
All-cause mortality
Description
all-cause mortality at 1-month and 6-months after treatment initiation
Time Frame
1 month; 6 months,

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 year-old First presentation of TTP/HUS Meet all of the following diagnostic criteria: Platelet count < 150 x 109 /L Microangiopathic haemolytic anaemia (blood film with presence of red blood cell fragmentation) LDH > 1.25 X the upper limits of normal No alternative diagnosis Exclusion Criteria: Secondary TTP/HUS Relapsing TTP/HUS Hypersensitivity to blood product Patient has received 2 or more plasma exchange treatment since symptom started over the last 1 week Received medication, including cyclosporine, cyclophosphamide, rituximab for treatment of TTP/HUS Other causes of thrombocytopenia than TTP/HUS
Facility Information:
Facility Name
Central Facility
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 4G5
Country
Canada

12. IPD Sharing Statement

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