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Short-course intensive sedative therapy of postoperative spontaneous intracerebral hemorrhage

Short-course intensive sedative therapy of postoperative spontaneous intracerebral hemorrhage

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OON-15006205
Enrollment
Unknown
Registered
2015-04-06
Start date
2011-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

intracerebral hemorrhage

Interventions

study group:short-course deep sedation therapy
control group:traditional sedation therapy

Sponsors

Affiliated Hospital of Taishan Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 79 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were met by patients with postoperative spontaneous intracerebral hemorrhage, surgical treatment refers to the traditional craniotomy hematoma removal and decompressive craniectomy. Drainage of ventricle can be done at the same time. But the surgery did not include hematoma puncture drainage or separate ventricular drainage.

Exclusion criteria

Exclusion criteria: Exclusion criteria included: preoperative GCS score was 3; the patient had respiratory failure and required the application of ventilator or already developed hypotension required vasopressor agents before operation; patients had cerebral hemorrhage or cerebral infarction medical history, and accompanied by obvious dysfunction with mRS score more than 3 points; operation doctor or close relatives of patients did not agree with the deep sedation therapy.

Design outcomes

Primary

MeasureTime frame
3 months mortality;3 months Modified Rankin Scale;ICU days;

Secondary

MeasureTime frame
postoperative SAS score;postoperative blood pressure in 12 hours;postoperative residual hematoma volume;the incidence of VAP;the incidence of re-operation;

Countries

China

Contacts

Public ContactDapeng Hou
hdptyfy@163.com+86 18505386932

Outcome results

None listed

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