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Registration Study for Cranioplasty in Enhanced Recovery After Surgery Mode and Traditional Mode

Registration Study for Cranioplasty in Enhanced Recovery After Surgery Mode and Traditional Mode

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900025105
Enrollment
Unknown
Registered
2019-08-11
Start date
2019-08-01
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

Cranial defect

Interventions

1:Cranioplasty in Enhanced Recovery After Surgery (ERAS)
2:Cranioplasty in Traditional Pattern

Sponsors

Department of neurosurgery, Tangdu Hospital, Airforce Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients with unilateral skull defects; 2. The defect area is >3cm; 3. Aged 18 to 65 years; 4. First surgery for cranioplasty; 5. Agree to use metal triple shape repair materials. 6. Sign the ERAS informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with mental illness or severe mental illness; 2. Women during pregnancy and lactation; 3. Participating in another clinical study; 4. Patients with advanced cancer or who are expected to die within 1 year; 5. The combined prognosis of hydrocephalus or wounds is poor, and the intraoperative flap should be transferred during the same period; 6. Serious neurological dysfunction; 7. Those who are allergic to metal repair materials;

Design outcomes

Primary

MeasureTime frame
Score of American Society of Anesthesiologists;Karnofsky Performance Scale;SF-36 score;Numeric Pain intensity Scale;Postoperative in-patient time;—

Countries

China

Contacts

Public ContactQu Yan

Tangdu Hospital, Airforce Military Medical University

bladerunnerwang@gmail.com+86 18629074363

Outcome results

None listed

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