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A cohort study of related techniques improvement in robotic minimally invasive procedure for intracranial hemorrhage

A cohort study of related techniques improvement in robotic minimally invasive procedure for intracranial hemorrhage

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300074881
Enrollment
Unknown
Registered
2023-08-18
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

intracranial hemorrhage

Interventions

modified techniques group:NA
traditional techniques group:NA

Sponsors

General Hospital of Northern Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Intracranial hemorrhage clearly diagnosed through clinical imaging; 2.Subjects aged = 18 years and = 75 years; 3.The patient is in a state of drowsiness, haziness, or light coma; 4.The patients or their families agree to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Have received Craniotomy treatment; 2. Patients in deep coma with dilated pupils on one or both sides; 3. Cerebral hemorrhage caused by cerebral arteriovenous malformations, aneurysms, and other reasons; 4. Brain tumor stroke; 5. Cerebral hemorrhage caused by hematological diseases and other factors; 6. Major surgeries planned within 30 days before or 90 days after enrollment; 7. Participated in clinical trials of other drugs or medical devices before being selected but did not meet the main research endpoint deadline; 8. Disabled before onset, which may interfere with functional outcome evaluation one year after surgery

Design outcomes

Primary

MeasureTime frame
Surgical results;NIHSS scores;

Secondary

MeasureTime frame
complications;GOS scores;ADL scores;

Countries

China

Contacts

Public ContactLiang Guobiao

General Hospital of Northern Theater Command

guobiaoliang@163.com+86 138 9886 6708

Outcome results

None listed

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