Completed

NACinTTPA Pilot Study of N-acetylcysteine in Suspected Thrombotic Thrombocytopenia Purpura

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What is being tested

N-Acetylcysteine

Drug
Who is being recruted

Cytopenia+13

+ Blood Coagulation Disorders

+ Blood Platelet Disorders

Over 18 Years
+12 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Early Phase 1
Interventional
Study Start: May 2013
See protocol details

Summary

Principal SponsorBloodworks
Last updated: September 20, 2017
Sourced from a government-validated database.Claim as a partner

Study start date: May 1, 2013

Actual date on which the first participant was enrolled.

Thrombotic thrombocytopenic purpura (TTP) is a rare hemostatic disorder with life threatening consequences secondary to microvascular thrombosis. While the use of therapeutic plasma exchange (TPE) has greatly improved survival, end organ damage, resistance to therapy, and relapses occur in many patients. Ultra-large von Willebrand factor multimers (ULVWF) are pathogenic in TTP. The investigators have found that N-acetylcysteine (NAC) cleaves ULVWF in vitro and in vivo in the ADAMTS13 deficient mice that are at increased risk of TTP. NAC is well tolerated in humans at intravenous doses used for treatment of acetaminophen overdose. This dosage correlates with that producing an effect in the murine studies noted above, and thus is an attractive treatment for patients with TTP. By cleaving VWF and preventing propagation of platelet/VWF strings, the investigators hypothesize that NAC treatment will decrease complications in patients with TTP receiving treatment with TPE. This will be manifest by a more rapid improvement in platelet count, decrease in number of days requiring plasma exchange, and decrease in microvascular thrombotic complications. To prepare for a larger trial the investigators propose a pilot study in 3 patients with suspected TTP at the University of Washington (UW) Medical Center. The study will be approved by the UW IRB prior to study initiation. Patients who consent to the study will receive daily NAC infusions beginning after the first TPE, in doses used for acetaminophen overdose. Blood samples will be collected for laboratory assays to determine optimal timing for sample collection in the larger multicenter trial, and to pilot the data collection forms. The investigators will also evaluate safety and patient tolerability.

Principal SponsorBloodworks
Last updated: September 20, 2017
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

3 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

CytopeniaBlood Coagulation DisordersBlood Platelet DisordersHematologic DiseasesHemic and Lymphatic DiseasesHemorrhagePathologic ProcessesPurpuraPurpura, ThrombocytopenicSigns and SymptomsSkin ManifestationsPathological Conditions, Signs and SymptomsThrombocytopeniaThrombophiliaThrombotic MicroangiopathiesPurpura, Thrombotic Thrombocytopenic

Criteria

5 inclusion criteria required to participate
Age >= 18 years of age

Anticipated TPE for > 5 days

Diagnosis of suspected TTP (lab evidence of hemolysis, platelet count < 120,000, schistocytes on peripheral smear)

Normal baseline prothrombin time (PT) and activated partial thromboplastin time (aPTT)

Show More Criteria

7 exclusion criteria prevent from participating
Asthma

Known allergy to NAC

Known underlying bleeding disorder

Life expectancy < 1 week

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
IV administration of N-acetylcysteine (Acetadote) at 150mg/Kg loading bolus over 60 minutes followed by 150mg/Kg over 17 hours if loading dose was well tolerated.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Puget Sound Blood Center

Seattle, United StatesOpen Puget Sound Blood Center in Google Maps
CompletedOne Study Center