SGLT2 Inhibitor Utilization Re-perfusion Therapy

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorTaichung Veterans General Hospital

About this trial

Background:

Reperfusion therapies, including intravenous rt-PA and mechanical thrombectomy, significantly improve outcomes in acute ischemic stroke. However, these interventions also increase the risk of hemorrhagic transformation and malignant edema. Preclinical studies have demonstrated that Canagliflozin, an SGLT2 inhibitor, reduces astrocyte swelling and brain edema in a transient middle cerebral artery occlusion (tMCAo) model. While SGLT2 inhibitors have shown neuroprotective effects in the acute phase of ischemic stroke, their potential to mitigate hemorrhagic transformation and malignant edema following reperfusion therapy in humans remains unexamined.

Aims:

This study aims to evaluate the effect of SGLT2 inhibitors on hemorrhagic transformation and malignant edema in patients undergoing reperfusion therapy for acute ischemic stroke.

Methods:

This is a multi-center, randomized, open-label, controlled study enrolling ischemic stroke patients aged 18 years or older who meet predefined inclusion and exclusion criteria. Participants will be randomized to receive Canagliflozin 100 mg once daily for 14 days or no additional treatment before undergoing mechanical thrombectomy. Clinical data collection will include baseline demographics, medical and medication history, NIHSS scores at admission and 24 hours post-reperfusion, stroke subtype, modified Thrombolysis in Cerebral Infarction (TICI) scores, laboratory results, and modified Rankin Scale (mRS) scores at discharge and 3 months post-stroke.

The primary outcome is to assess the association between Canagliflozin use and the severity of hemorrhagic transformation and malignant edema. Hemorrhagic transformation will be classified using the Heidelberg criteria, and malignant edema will be defined as a midline shift of ≥5 mm. Brain imaging, including CT scans at 24 hours post-intervention and additional scans as clinically indicated, will be reviewed by blinded radiologists. Brain MRA will also be performed to assess infarct size and edema progression.

Importance:

This study aims to explore the potential for repurposing SGLT2 inhibitors as a therapeutic strategy in acute ischemic stroke. If Canagliflozin is shown to reduce hemorrhagic transformation and malignant edema, it could offer a novel adjunctive treatment to improve patient outcomes following reperfusion therapy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients must have been diagnosed with acute ischemic stroke and large vessel occlusion by a neurologist, with confirmation supported by CT perfusion scans.

Patients must be scheduled to undergo mechanical thrombectomy.

Disqualifiers

Patients with have stage 4 or 5 chronic kidney disease (estimated glomerular filtration rate (eGFR) below 30 mL/min/1.73 m² on dialysis)

Patients with currently taking an SGLT2i or within 3 months prior to enrollment

Patients with a known hypersensitivity or allergic reaction to Canagliflozin

Patients with type 1 diabetes mellitus

Trial design

Design model

Single group

Treatments tested in this trial

  • Canagliflozin 100mg

    Drug

    receiving Canagliflozin 100mg QD

Treatment groups

150 Participants
are divided into 2 treatment groups
Group A: study groupExperimental treatment 1 intervention
Group B: control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Occurrence of malignant edema

Diagnosed if midline shift ≥5 mm on brain imaging or symptomatic brain swelling requiring decompressive craniectomy, leading to in-hospital death, or coma at discharge.

Time frame
On the 3rd to 5th day for MRI after EVT
2

mRS at 3rd month after stroke onset

Assesses health-related quality of life using modified Rankin Scale (mRS) to assess disability level post-stroke for understanding the recovery situation of the patient.

Time frame
3 months after stroke onset
3

Mortality rate at 3rd month after stroke onset

To understand if the patient is surviving or not after stroke onset.

Time frame
After stroke onset in 3 months.

Secondary outcomes

1

Occurrence of hemorrhagic transformation

Classified using the Heidelberg criteria to categorize hemorrhagic changes post-EVT.

Time frame
During hospitalization for 14 days
2

Occurrence f parenchymal hematoma type2

Identified based on brain imaging and classified using the Heidelberg criteria, indicating severe hemorrhagic transformation.

Time frame
During hospitalization for 14 days
3

NIHSS 24 hours later

Neurological status assessed using National Institutes of Health Stroke Scale (NIHSS) to measure stroke severity and potential deterioration by neurologist.

Time frame
24 hours after EVT
4

mRS at discharge

Functional outcome evaluated using modified Rankin Scale (mRS) to assess disability level post-stroke.

Time frame
Day 14 at hospital discharge

Other outcomes

1

Occurrence of adverse events as assessed by CTCAE v5.0

To understand if the patient have any occurrence of AE or SAE during the session. The result of finding any of the diseases listed on the CTCAE v5.0 will be reported to IRB of Taichung Veterans General Hospital.

Time frame
During hospitalization for 14 days

Locations

This trial has no locations.

Sponsors and contacts

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