Clinical Trials Directory

Trials / Completed

CompletedNCT04522102

Antiplatelet Secondary Prevention International Randomised Trial After INtracerebral HaemorrhaGe (ASPIRING)-Pilot Phase

An Investigator Initiated and Conducted, Prospective, Multicentre, Randomised Outcome-blinded Pilot Study of Antiplatelet Therapy in Patients with a History of Stroke Due to Intracerebral Haemorrhage

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
80 (actual)
Sponsor
The George Institute for Global Health, China · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

ASPIRING is an investigator-led, multicentre, prospective, randomised, open-label, blind outcome (PROBE), parallel group, clinical trial. The pilot phase will explore the feasibility of conducting a trial of starting antiplatelet monotherapy versus avoiding antiplatelet therapy for reducing all serious vascular events for adults surviving symptomatic stroke due to spontaneous intracerebral haemorrhage (ICH). The pilot phase will involve \~120 patients at \~30 hospitals in China, Australia and New Zealand.

Detailed description

The participant eligibility criteria specifically identify adults with history of symptomatic spontaneous ICH. Randomisation occurs if a participant and their doctor are uncertain about whether to start or avoid antiplatelet monotherapy at least 24 hours after ICH symptom onset. The intervention is a pragmatic policy of starting antiplatelet monotherapy (one antiplatelet drug available in local standard clinical practice, chosen by patient's physician pre-randomisation). The control group adopts a policy of avoiding antiplatelet therapy.

Conditions

Interventions

TypeNameDescription
DRUGStart antiplatelet monotherapyStart one antiplatelet drug, be available in local standard clinical practice, chosen by patient's physician pre-randomisation

Timeline

Start date
2021-09-03
Primary completion
2023-10-13
Completion
2023-10-13
First posted
2020-08-21
Last updated
2025-03-26

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT04522102. Inclusion in this directory is not an endorsement.