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A Greek-designed ERAS Protocol in Elective Craniotomy

A Greek-designed Enhanced Recovery After Surgery (ERAS) Protocol in Elective Cranial Neurosurgical Procedures: An Observational Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05962684
Acronym
ERAS
Enrollment
30
Registered
2023-07-27
Start date
2023-05-31
Completion date
2024-07-30
Last updated
2023-07-27

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

Conditions

Craniotomy, ERAS

Keywords

ERAS, Craniotomy, Perioperative management

Brief summary

The implementation of ERAS protocol in elective cranial neurosurgical cases in a tertiary hospital.

Detailed description

In this study, the investigators have integrated the most current data from literature aiming to investigate the effectiveness of a contemporary ERAS protocol for elective cranial neurosurgical cases in a tertiary hospital. The hypothesis is that the implementation of such protocol will shorten the postoperative length of stay, minimize the complication rates, and improve the overall clinical status of patients undergoing elective craniotomy compared to the standard perioperative care

Interventions

OTHERERAS

Implementation of ERAS protocol in elective craniotomy patients

Sponsors

University of Thessaly
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Medically suitable for elective craniotomy * ASA-PS I-III

Exclusion criteria

* traumatic lesions * pathology requiring emergent surgery * preoperative loss of consciousness * severe co-morbidities that may affect postoperative recovery (e.g. paralysis, autoimmune diseases, myocardial or severe infarction, heart, liver or lung malfunction, severe mental illness etc.) * recurrent tumor

Design outcomes

Primary

MeasureTime frameDescription
Hospital Length of Stayup to 7 daysThe days the patient stays in hospital

Secondary

MeasureTime frameDescription
Pain scorePostoperative Day 1 to discharge, an average of 7 daysPain intensity as measured by Visual Analogue Scale (VAS)
Mental status1 day at dischargeMental status as measured by Glasgow Coma Scale (GCS) Minimum value : 3 Maximum value : 15 Higher scores mean a better outcome
Patient's satisfaction1 day at discharge and 1 month postoperativelyPatient's satisfaction as measured by a Likert Scale
Anxiety and DepressionPreoperatively, second postoperative day and one month postoperativelyAnxiety and Depression level as measured by Hospital Anxiety and Depression Scale (HADS)
Personality IndexPreoperatively, second postoperative day and one month postoperativelyPersonality Index as measured by TIPI

Countries

Greece

Contacts

Primary ContactEleni Arnaoutoglou, MD, PhD
earnaout@gmail.com+306974301352
Backup ContactMetaxia Bareka, MD, PhD
barekametaxia@hotmail.com+306947845083

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026