An Open-Label, Dose-Escalation Study on the Safety, Tolerability and Preliminary Efficacy for Preventing SAP by Intravenous Pump-Delivered Propranolol in Patients With ICH

Starting soon · Phase 1

Conditions studied: Intracerebral Hemorrhage, Stroke-Associated Pneumonia (SAP)

In brief

This is an open-label, dose-escalation study on the safety, tolerability and preliminary efficacy for preventing stroke-associated pneumonia of propranolol in patients with intracerebral hemorrhage. Propranolol is administered via intravenous pump continuously for 7 days.

Key facts

Study ID
NCT07528235
Run by
Tang-Du Hospital
People needed
30
Starts
2026-05-01
Expected to finish
2026-11-01
Last updated by the study team
2026-04-14

Who can join

Age: 10 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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