Combination of Targeted Temperature Management and Thrombectomy After Acute Ischemic Stroke (COTTIS-2) - a Randomised Controlled Study

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

The goal of this clinical trial is to test the combination of hypothermia and endovascular treatment in acute stroke patients with large vessel occlusion. The main question it aims to answer is: does an additional cooling to 35°C result in a benefit on clinical outcome ? Participants receive immediate cooling using a noninvasive transnasal cooling technique (RhonoChill) and are maintained at 35°C for 6 hours after reopening of the vessel using surface cooling, and then slowly rewarmed. Researchers will compare the intervention group (hypothermia and endovascular treatment and best medical treatment including iv thrombolysis) and control group (only endovascular treatment and best medical treatment including iv thrombolysis) to see if additional hypothermia leads to a better outcome after 3 months without relevant complications.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Pre-stroke modified Rankin Scale (mRS) 0-2 \[7-point scale rating from 0 (no symptoms) to 6 (dead)\]

• Acute ischemic stroke with NIHSS \>5

• Intracranial occlusion of the M1 or M2 segment of the middle cerebral artery (MCA) or internal carotid artery (ICA) or tandem occlusion on CT-angiography or MR-angiography with indication for endovascular treatment:

• Time window 0-24h:

‣ Last seen normal to groin puncture \< 6h: native CT or MRI-DWI with ASPECTS \>5

⁃ Last seen normal to groin puncture 6-24h or unknown time window: significant mismatch imaging according to the eligibility criteria of the DEFUSE-3 trial

• Infarct core \<70ml (DWI oder CBF\<30%)

∙ Penumbra \> 15ml (Tmax \>6sec)

∙ Ratio penumbra/core \>1.8

• with or without iv thrombolysis with rtPA

Locations
Other Locations
Germany
University of Freiburg, Department of Neurology
RECRUITING
Freiburg Im Breisgau
Contact Information
Primary
Juergen Bardutzky, Prof.
juergen.bardutzky@uniklinik-freiburg.de
+49-15237729739
Backup
Wolf-Dirk Niesen, PD Dr.
wolf-dirk.niesen@uniklinik-freiburg.de
0049-761-270-53050
Time Frame
Start Date: 2024-07-07
Estimated Completion Date: 2026-06-18
Participants
Target number of participants: 400
Treatments
No_intervention: EVT group
standard endovascular treatment (EVT) for large vessel occlusion (LVO) without hypothermia
Active_comparator: EVT group plus hypothermia group
standard endovascular treatment (EVT) for large vessel occlusion (LVO) combined with hypothermia
Related Therapeutic Areas
Sponsors
Leads: University of Freiburg
Collaborators: European Union, Center for Medical data science, University of Vienna, Austria, E+E CRO consulting, Vienna, Austria

This content was sourced from clinicaltrials.gov

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