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Clinical study protocol for the study of goal-directed volume management combined with TCCD in the perioperative period in patients with aSAH

Clinical study protocol for the study of goal-directed volume management combined with TCCD in the perioperative period in patients with aSAH

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062551
Enrollment
Unknown
Registered
2022-08-11
Start date
2022-10-10
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

aSAH

Interventions

conventional fluid therapy group:conventional fluid therapy
GDT group:GDT

Sponsors

Mianyang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients with aneurysmal SAH diagnosed by CT and confirmed by angiography were eligible for enrollment; 2. Age 18 to 80 years; 3. Those who were fully informed and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Traumatic SAH; 2. Secondary craniosynostosis; 3. Congestive heart failure; 4. Severe aortic or aortic valve disease; 5. Pregnancy and poor calcium antagonist tolerance; 6. Patients deemed unsuitable for enrollment by the investigator.

Design outcomes

Primary

MeasureTime frame
pulsatility index(PI);Lindegaard;intracranial pressure(ICP);cerebral perfussion pressure(CPP);—

Countries

China

Contacts

Public ContactXu Zhihua

Mianyang Central Hospital

yokiku163@163.com+86 13890199910

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026