Optimising Circulatory Blood Volume after Aneurysmal Subarachnoid Hemorrhage.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON25625

Enrollment

100

Registered

2008-03-22

Start date

2006-01-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

subarachnoid hemorrhage

Interventions

Measurement of circulating blood volume (CBV) is performed daily in all included patients, by means of Pulse Dye Densitometry. Patients in the intervention group (n=50) have fluid management based on

Eligibility

Inclusion criteria

Inclusion criteria: 1. Aneurysmal subarachnoid hemorrhage; 2. Admitted to UMC Utrecht within 72 hours after the SAH.

Exclusion criteria

Exclusion criteria: 1. Imminent death; 2. Liver failure; 3. Kidney failure; 4. Pregnancy; 5. Possible allergy to indocyanine green; 6. Accompanying head injury.

Design outcomes

Primary

Measure	Time frame
The occurrence of severe hypovolemia, defined as CBV < 50 ml/kg.	—

Secondary

Measure	Time frame
The relation between CBV values and the presence of delayed cerebral ischemia, pulmonary edema, and the use of inotropic support.	—

Contacts

Public ContactReinier G. Hoff

Department of Perioperative & Emergency Care, University Medical Center Utrecht.

r.hoff@umcutrecht.nl+31 (0)88 7559475

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)