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A Greek-designed ERAS Protocol in Elective Craniotomy

U

University of Thessaly

Status

Enrolling

Conditions

ERAS
Craniotomy

Treatments

Other: ERAS

Study type

Observational

Funder types

Other

Identifiers

NCT05962684
ERAS Craniotomy

Details and patient eligibility

About

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

Full 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

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

30 participants in 1 patient group

ERAS
Treatment:
Other: ERAS

Trial contacts and locations

1

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Central trial contact

Metaxia Bareka, MD, PhD; Eleni Arnaoutoglou, MD, PhD

Data sourced from clinicaltrials.gov

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