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RISK FACTORS FOR FAILED EXTUBATION IN THE OPERATING ROOM, IN POSTOPERATIVE NEUROSURGERY PATIENTS

Factors Influencing Failed Extubation in the Operating Room: A Study of Postoperative Neurosurgery Patients - FIEEOR: Factors Influencing Failed Extubation in the Operating Room.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000056751
Enrollment
82
Registered
2025-02-17
Start date
2024-05-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Postoperative neurosurgery recovery. This study focuses on patients who have undergone neurosurgical procedures and are in the recovery phase. We aim to evaluate the risk factors associated with failed extubation in the operating room during this critical post-anesthesia period.

Interventions

Control Group (Group B): Patients who successfully extubated during general anesthesia in the operating room and were able to maintain spontaneous ventilation without ventilatory support for 48 hours

Sponsors

U.M.A.E. Specialized Hospital Dr. Antonio Fraga Mouret of the National Medical Center La Raza of the I.M.S.S. U.N.A.M.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients of both genders aged 18 years and older. Patients who have undergone neurosurgery and were extubated during the anesthesia procedure in the operating room. Patients who are able to maintain spontaneous ventilation without ventilatory support for 48 hours post-neurosurgery (for the control group). Patients who experienced failed extubation and required re-intubation within the first 48 hours post-neurosurgery (for the case group).

Exclusion criteria

Exclusion criteria: Patients who were intubated upon leaving the operating room. Patients with incomplete medical records or those who had missing documentation. Patients who experienced loss of record of their surgical procedure. Patients who had significant pre-existing medical conditions that may affect the extubation process (e.g., severe respiratory disorders).

Design outcomes

Primary

MeasureTime frame
Incidence of Failed Extubation: The primary outcome measure will be the incidence of failed extubation within the first 48 hours post-neurosurgery. This will be assessed by identifying patients from Group A who required re-intubation and recording the number of such cases. Timing of Measurement: The incidence will be measured at the 48-hour postoperative mark.

Countries

North America

Contacts

Public ContactMOISES ALMARAZ

IMSS ANESTESIOLOGY

yuseimoy@gmail.com5584244399

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026