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The correlation of cranioplasty and the improvement of cerebral blood flow and the recovery of neual function: single center clinical trial

The correlation of cranioplasty and the improvement of cerebral blood flow and the recovery of neual function: single center clinical trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-17012875
Enrollment
Unknown
Registered
2017-10-03
Start date
2017-10-01
Completion date
Unknown
Last updated
2017-10-09

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

Conditions

cranioplasty

Interventions

early group and late group:Computed tomography perfusion (CTP) and transcranial Doppler (TCD)

Sponsors

First Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. from eighteen to sixty-five years old; 2. performed DC for the reasons of traumatic cerebral hemorrhage, rupture of aneurysm or hypertensive cerebral hemorrhage and need to perform craniolasty; 3.the skull defect is located at the area of superior tentorium of cerebellum and defective diameter is larger than 3 cm

Exclusion criteria

Exclusion criteria: 1. posterior fossa skull defect; 2. patients with severe lung, liver and kidney diseases; 3. with severe blood and central nervous system infection before cranioplasty; 4. patients with severe hydrocephalus; 5. others need to terminate the study due to unexpected causes.

Design outcomes

Primary

MeasureTime frame
CBF, CBV, TTP, MTT, Vp, Vm, PI, RI;

Countries

China

Contacts

Public ContactMei-hua Li
limeihua2000@sina.com+86 13970052318

Outcome results

None listed

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