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The Clinical Study for Cerebral Corridor Creator

The Clinical Study of Cerebral Corridor Creator

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024727
Enrollment
Unknown
Registered
2019-07-25
Start date
2016-05-01
Completion date
Unknown
Last updated
2019-07-29

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

Conditions

Hydrocephalus, Cerebral Infarction, intracranial tumour

Interventions

Control Group:Metal Brain Pressure Plate
Experimental group:Cerebral Corridor Creator to be used in the craniocerebral operation

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. The patients age is controlled within 18 and 70 years old male and female; 2. The patients with cerebral cortex and cerebral ventricles who need the craniotomy operation diagnosed by imaging examination or intracranial operation; 3. The patients and their families are subject to the programme of the competent physician, who accept voluntarily the clinical study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Terminal cerebral hernia; 2. Severe visceral disease; 3. Pregnant women and patients with possible pregnancy; 4. Patients with intracranial aneurysm vascular malformation; 5. severe coagulation disorders, intracranial tumour; 6. The patients and their families refuse the operation.

Design outcomes

Primary

MeasureTime frame
Amount of bleeding in operation;

Secondary

MeasureTime frame
Skin Incision Length;lesion residual;Bone Window Area;Cortical Incision Area;Hospital Stay;

Countries

China

Contacts

Public ContactLi Weiping

Shenzhen Second People's Hospital

Liweiping60@139.com+86 13808834238

Outcome results

None listed

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