Hypercapnia to Prevent Secondary Ischemia in SAH
- Conditions
- Aneurysmal Subarachnoid Hemorrhage
- Interventions
- Procedure: Hypercapnia by reduction of respiratory volume
- Registration Number
- NCT01799525
- Lead Sponsor
- Wuerzburg University Hospital
- Brief Summary
Delayed cerebral vasospasm and secondary ischemic infarction are feared complications after aneurysmal subarachnoid hemorrhage (aSAH). To date, there is no effective therapy to prevent these ischemic complications. The arterial partial pressure of carbon dioxide (PaCO2) is one of the main determinants of cerebral blood flow (CBF) in healthy subjects. It is yet largely unknown, if and to what extent modulations of PaCO2 can influence CBF in patients after aSAH. The trial is a phase 1 study in which the feasibility of hypercapnia in SAH patients is tested. PaCO2 is gradually raised to 60 mmHg in 10 mechanically ventilated aSAH patients. Cerebral oxygen saturation measured by NIRS and CBF determined by an intracerebral thermodilution probe are the primary end points. If the feasibility is confirmed, this trial will be followed by a phase 2 dose finding study.
- Detailed Description
The course of aneurysmal subarachnoid hemorrhage (aSAH) is determined by the sequence of several ischemic episodes. Immediately after aSAH, an increase of ICP causes an increase of CBF. It is followed by an acute vasoconstriction over the next hours and days. Typically between day 4 and 10 after aSAH, delayed arterial narrowing and a decrease of CBF occurs in approximately 50 % of aSAH patients and may result in cerebral ischemia and infarction. After the failure of the CONSCIOUS-trial to improve outcome after aSAH, there is no specific treatment in sight to effectively prevent cerebral ischemic events after aSAH. Under physiological conditions, the arterial partial pressure of carbon dioxide (PaCO2) is one of the main determinants of cerebral blood flow (CBF). An elevation of PaCO2 may also be a useful treatment on aSAH patients. This trial is designed as a phase 1 study to test the feasibility of controlled hypercapnia in mechanically ventilated aSAH patients with poor-grade SAH. Monitoring is performed by an external ventricular drainage (ICP), near infrared spectroscopy (tissue oxygenation) and a thermodilution probe (CBF). The latter monitoring tools represent the primary end points of this study. In case of affirmed feasibility, a dose finding study will be launched as a next step.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 10
- aneurysmal SAH
- SAH Hunt/Hess Grade 3-5
- SAH Fisher Grade 2-4
- Mechanically ventilated
- external ventricular drainage/ICP measurement
- Age under 18
- ICP > 25 mmHg for > 2 minutes
- pH < 7.250
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Hypercapnia Hypercapnia by reduction of respiratory volume Intervention: SAH patients are subjected to gradual hypercapnia by reduction of respiratory volume in one trial session every day. PaCO2 is raised from normocapnia to 50 mmHg for 10 - 15 minutes and 60 mmHg for 10 - 15 minutes.
- Primary Outcome Measures
Name Time Method Cerebral Blood Flow For an average of two weeks after aSAH Between day 4 and 14, PaCO2 is gradually raised from normocapnic values (40 mmHg) to hypercapnic values (50 and 60 mmHg). CBF is continuously measured during this intervention. Patients are clinically and radiologically followed for 6 months.
- Secondary Outcome Measures
Name Time Method intracranial pressure (ICP) For an average of two weeks ICP is continuously measured by an external ventricular drainage throughout the intervention period.
Cerebral oxygen saturation For an average of two weeks after aSAH Oxygen saturation by NIRS is measured continuously for 2 weeks after aSAH.
Trial Locations
- Locations (1)
Department of Neurosurgery, University of Wuerzburg
🇩🇪Wuerzburg, Bavaria, Germany