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Effect of Remote Ischemic Conditioning on Cerebral Hemodynamics in Patients After Intravenous Thrombolysis (RICCH-IVT)

Effect of Remote Ischemic Conditioning on Cerebral Hemodynamics in Patients After Intravenous Thrombolysis (RICCH-IVT)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05598658
Enrollment
100
Registered
2022-10-28
Start date
2023-04-01
Completion date
2024-04-12
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Remote Ischemic Conditioning

Keywords

Remote Ischemic Conditioning, Intravenous Thrombolysis, Cerebral Hemodynamics, Cerebral Autoregulation, Cerebral Blood Flow Velocity

Brief summary

The purpose of this study is to determine the effect of remote ischemic conditioning on cerebral hemodynamics in patients after intravenous thrombolysis

Detailed description

In this study, cases of ischemic stroke who undergo intravenous thrombolysis within 4.5 hours from onset are included. The RIC group receive basic treatment and remote ischemic conditioning for 200mmHg at 6 and 18-24 hours after intravenous thrombolysis. The sham-RIC group receive basic treatment and remote ischemic conditioning for 60mmHg at 6 and 18-24 hours after intravenous thrombolysis. Both groups underwent cerebral hemodynamics after RIC and recorded the relevant indexes. The investigators aimed to determine the effect of remote ischemic conditioning on cerebral hemodynamics in patients after intravenous thrombolysis.

Interventions

PROCEDURERemote ischemic conditioning

Remote ischemic conditioning (RIC) is induced by 4 cycles of 5 min of healthy upper limb ischemia followed by 5 min reperfusion. Limb ischemia was induced by inflations of a blood pressure cuff to 200 mm Hg.

PROCEDURESham remote ischemic conditioning

Sham remote ischemic conditioning (RIC) is induced by 4 cycles of 5 min of healthy upper limb ischemia followed by 5 min reperfusion. Limb ischemia was induced by inflations of a blood pressure cuff to 60 mm Hg.

Sponsors

Yi Yang
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. age ≥ 18 and \< 80 years, both sexes; 2. a clear clinical diagnosis of acute ischemic stroke and treatment with standard rt-PA (0.9 mg/kg) IVT within 4.5 h of stroke onset; 3. pre-onset modified Rankin Scale (mRS) score ≤1; 4. baseline National Institute of Health Stroke Scale (NIHSS) score ≥5 and ≤25; 5. Glasgow Coma Scale score ≥8.

Exclusion criteria

1. having received bridging therapy (IVT plus mechanical thrombectomy); 2. previous history of atrial fibrillation or electrocardiographic evidence of atrial fibrillation; 3. contraindications to RIC treatment or previous RIC treatment or similar treatment; 4. pregnancy or breastfeeding; 5. life expectancy of ≤3 months or inability to complete the study for other reasons; 6. unwillingness to be followed up or poor treatment compliance or participation in other clinical studies; 7. had insufficient bilateral temporal bone windows for insonation of the middle cerebral artery.

Design outcomes

Primary

MeasureTime frameDescription
Cerebral autoregulation parameter1-10 daysCerebral autoregulation parameters derived from transfer function analysis. Continuous cerebral blood flow velocities of bilateral middle cerebral artery will be assessed noninvasively using transcranial Doppler. Spontaneous arterial blood pressure will be simultaneously recorded using a servo-controlled plethysmograph on the left or right middle finger with an appropriate finger cuff size. Transfer function analysis will be used to derive the autoregulatory parameter.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026