Skip to content

Registration Study for Geriatric Brain Tumor in Enhanced Recovery After Surgery Protocol and Traditional Protocol

Registration Study for Geriatric Brain Tumor in Enhanced Recovery After Surgery Protocol and Traditional Protocol

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900025106
Enrollment
Unknown
Registered
2019-08-11
Start date
2019-08-12
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

Geriatric brain tumor

Interventions

1:ERAS mode
2:traditional treatment mode

Sponsors

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

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. According to the preoperative imaging examination, the initial diagnosis of intracranial tumor patients requiring craniotomy intervention; 2. Subject aged >= 60 years; 3. Subjects have a Karnofsky score of >= 70 before surgery; 4. Sign the ERAS project informed consent form.

Exclusion criteria

Exclusion criteria: 1. Postoperative pathology confirmed non-tumor patients 2. The subject is an intracranial recurrent tumor; 3. Subjects were multiple lesions or multiple brain lobe lesions. 4. Subjects have neurological dysfunction, such as hemiplegia and aphasia, before surgery, which cannot be combined with clinical research; 5. The subject has other malignancies at the same time; 6. Any unstable severe systemic disease (including active infections, uncontrolled high blood pressure, unstable angina pectoris, angina pectoris that has started within the last 3 months, congestive heart failure, 12 months prior to enrollment Intramyocardial infarction, severe arrhythmia requiring medication, liver, kidney or metabolic disease); 7. Within 30 days of the start of the study or participating in other clinical studies; 8. Other investigators believe that it is not suitable for enrollment.

Design outcomes

Primary

MeasureTime frame
Score of American Society of Anesthesiologists;Karnofsky Performance Scale;Numeric Pain intensity Scale;Postoperative in-patient time;MoCA Scale;Charlesson comorbidity index;FRAIL SCALE Weakness Scale;NSA2000;

Countries

China

Contacts

Public ContactWang Liang

Tangdu Hospital, Airforce Military Medical University

bladerunnerwang@gmail.com+86 13319231049

Outcome results

None listed

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