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Aneurysmal Subarachnoid Hemorrhage and Superior Mesenteric Artery Flow Study

Evaluation of Superior Mesenteric Artery Diameter and Flow in Aneurysmal Subarachnoid Hemorrhage Patients Undergoing Hypertensive Therapy for Cerebral Artery Vasospasm

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02684500
Enrollment
14
Registered
2016-02-18
Start date
2016-04-11
Completion date
2016-06-30
Last updated
2020-03-19

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

Conditions

Intracranial Aneurysm

Keywords

aSAH

Brief summary

The purpose of this research study is to determine if the diameter and flow of the superior mesenteric artery in patients with aneurysmal subarachnoid hemorrhage undergoing hypertensive therapy for cerebral artery vasospasm are effected enough to justify withholding enteral nutrition.

Detailed description

Study measurements of the diameter and Doppler flow velocity of the superior mesenteric artery (SMA) using abdominal ultrasound in order to evaluate the potential additional risk of non-occlusive mesenteric ischemia (NOMI) and non occlusive bowel necrosis (NOBN) in patients undergoing hypertensive therapy for cerebral vasospasm in Aneurysmal Subarachnoid Hemorrhage (aSAH), to justify the withholding of enteral nutrition.

Interventions

DEVICEUltrasound

Study measurements of the diameter and doppler flow velocity of the superior mesenteric artery (SMA) for a aneurysmal subarachnoid hemorrhage using abdominal ultrasound.

Sponsors

University of Florida
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Patient diagnosed with aSAH

Exclusion criteria

* Hemodynamic instability * Already receiving vasopressor therapy * Non-aneurysmal SAH * Intracranial hemorrhage of other cause * Not anticipated to receive hypertensive therapy with vasoactive medications for cerebral vasospasm from SAH or suspected aSAH * Unable to visualize SMA using ultrasound * Pregnancy

Design outcomes

Primary

MeasureTime frame
Change between baseline and 21 days of abdominal ultrasound measurement of the diameter in the superior mesenteric arteryChange from baseline up to 21 days
Change between baseline and 21 days of abdominal ultrasound measurement of the doppler flow velocity in the superior mesenteric arteryChange from baseline up to 21 days

Secondary

MeasureTime frameDescription
Number of participants with non-occlusive mesenteric ischemia (NOMI)Change from baseline up to 21 daysNumber of participants with non-occlusive mesenteric ischemia (NOMI) undergoing hypertension therapy with vasoactive medications for cerebral arterial vasospasm in aneurysmal subarachnoid hemorrhage (aSAH).
Number of participants with non occlusive bowel necrosis (NOBN)Change from baseline up to 21 daysNumber of participants with non occlusive bowel necrosis (NOBN) undergoing hypertension therapy with vasoactive medications for cerebral arterial vasospasm in aneurysmal subarachnoid hemorrhage (aSAH).

Countries

United States

Outcome results

None listed

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