Clinical study of intracranial pressure balancing device in the treatment of postoperative complications after Decompressive Craniectomy

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000032506

Enrollment

Unknown

Registered

2020-04-30

Start date

2020-06-01

Completion date

Unknown

Last updated

2020-06-15

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

Conditions

complications after Decompressive Craniectomy

Interventions

experimental group:To use intracranial pressure balancing device

control group:Nil

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Those patients with cerebral contusion and laceration, cerebral hemorrhage, cerebral infarction, compression of ventricles and displacement of midline were confirmed by CT; 2. Patients with preoperative GCS <= 8; 3. The patient / family member is informed and signs the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with serious primary diseases; 2. Patients with coagulation dysfunction; 3. Patients with unstable vital signs; 4. Patients who can not tolerate surgery; 5. Patients with postoperative intracranial rebleeding or cerebral infarction; 6. Patients with intracranial pressure greater than 250mmh2o after decompressive craniectomy; 7. Patients with high skin flap tension; 8. Patients with incomplete postoperative clinical data; 9. Patients participating in other clinical studies.

Design outcomes

Primary

Measure	Time frame
Brain CT scan;Cerebral perfusion;Prognostic evaluation;	—

Countries

China

Contacts

Public ContactJinping LI

Beijing Chaoyang Hospital Affiliated to Capital Medical University

ljp6855@aliyun.com+86 13910657387

Outcome results

None listed

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