Clinical Trials Directory

Trials / Terminated

TerminatedNCT04920448

N-ACETYLCYSTEINE FOR THROMBOLYSIS IN ACUTE STROKE

TOLERANCE STUDY OF N-ACETYLCYSTEINE FOR THROMBOLYSIS IN THE ACUTE PHASE OF ISCHEMIC STROKE / ETUDE DE TOLERANCE DE LA N-ACETYLCYSTEINE POUR LA THROMBOLYSE A LA PHASE AIGUË DE L'INFARCTUS CEREBRAL

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
12 (actual)
Sponsor
University Hospital, Caen · Academic / Other
Sex
All
Age
18 Years – 86 Years
Healthy volunteers
Not accepted

Summary

The primary objective of the study is to assess the safety of N-Acetylcysteine as a thrombolytic agent in acute ischemic stroke, especially regarding the risk of hemorrhagic transformation.

Detailed description

Preclinical studies demonstrated that N-Acetylcysteine (NAC) is able to break von Willebrand Factor (VWF) multimers by bisulfide bond reduction. Since thrombi in stroke patients are rich in VWF, NAC could be used as a thrombolytic agent during the acute phase. This study aims at assessing the safety of NAC in combination with alteplase (rt-PA) at the acute phase of ischemic stroke.

Conditions

Interventions

TypeNameDescription
DRUGN-Acetyl cysteineAdministered as specified in the treatment arm

Timeline

Start date
2021-06-16
Primary completion
2023-04-25
Completion
2024-04-25
First posted
2021-06-09
Last updated
2025-07-25

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04920448. Inclusion in this directory is not an endorsement.