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Efficacy Study II on Remote Ischemic Conditioning for the Prevention of Stroke-Associated Pneumonia

NCT05982015 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1651

Last updated 2024-12-27

No results posted yet for this study

Summary

Verifying whether remote ischemic adaptation can reduce the occurrence of stroke related pneumonia in acute stroke patients within 24 hours of onset

Conditions

Interventions

DEVICE

Remote ischemic conditioning

The RIC procedure consists of five cycles of unilateral arm ischemia for 5 minutes, which was followed by reperfusion for another 5 minutes. The procedure is performed with an electric, autocontrol device with a cuff that inflated to a pressure of 200 mmHg during the ischemia period. RIC is performed within 24hours after stroke onset, and twice daily for the subsequent 7 days.

DEVICE

Sham remote ischemic conditioning

The RIC procedure consists of five cycles of unilateral arm ischemia for 5 minutes, which was followed by reperfusion for another 5 minutes. The procedure is performed with an electric, autocontrol device with a cuff that inflated to a pressure of 60 mmHg during the ischemia period. RIC is performed within 24hours after stroke onset, and twice daily for the subsequent 7 days.

Sponsors & Collaborators

  • Capital Medical University

    lead OTHER

Principal Investigators

  • Chuanjie Wu, M.D. · Xuanwu Hospital of Capital Medical University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-22
Primary Completion
2024-09-19
Completion
2024-12-19

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05982015 on ClinicalTrials.gov