The Effect of Cerebral Oxygenation on Postoperative Recovery in Intracranial Surgery

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03714347

Acronym

Oxygenation

Enrollment

100

Registered

2018-10-22

Start date

2016-12-28

Completion date

2019-01-31

Last updated

2018-10-22

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

Conditions

Intracranial Neoplasm

Keywords

cerebral oxygen monitoring, intracranial surgery, general anesthesia

Brief summary

The aim of this study was to investigate the effect of cerebral oxygenation on postoperative compilation in intracranial surgery.

Detailed description

Patients undergoing intracranial surgery will be divided into two groups; group (Group Control n = 100) and cerebral oxygenation monitoring group (Group Oxygen). all hemodynamic parameters such as systolic blood pressure and diastolic blood pressure, oxygen saturation, Et CO2, SpO2;% and BIS during anesthesia during anesthesia will be recorded intraoperatively and 10 postoperatively in 5 min intervals. After extubation, Modified Aldrete Score, GKS (Glasgow Coma Scale), Ramsey Sedation Scale (RSS), nausea-vomiting and pain will be recorded in the recovery room. Pain assessment will be done with Visual Analog Scale (VAS). Patient satisfaction will be recorded. MMST (mini mental state test) and ASEM (antisaccadic eye movement test) tests will be performed preoperatively and postoperatively at 1st, 2nd and 3rd days.

Interventions

DEVICEcerebral oxygen monitoring

probes will be placed on eyebrows on forehead

DEVICEroutine monitoring

We will use routine monitoring intervention such as hate rate, arterial pressure, BIS. cerebral oxygen monitoring will not be applied to this group

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender

ALL

Age

25 Years to 75 Years

Healthy volunteers

Inclusion criteria

* Intracranial surgery will be performed * Age 25-75 * ASA in the I-II-III risk group

Exclusion criteria

* Under GKS 15 * heart failure, * renal insufficiency, * liver failure, * congenital neurological deficits

Design outcomes

Primary

Measure	Time frame	Description
cerebral oxygen monitoring data	cerebral oxygen values reported will be measured at 10 min intervals (intraoperative) and It would be reported by the first postoperative 10 minute intervals up to 30 minutes	cerebral oxygen monitoring will measure peroperative

Countries

Turkey (Türkiye)

Contacts

Primary ContactSevtap Hekimoglu Sahin, Professor

sevtaphekimoglu@mynet.com

Backup ContactBeyhan Karamanlıoglu, professor

beykar@mynet.com

Outcome results

None listed

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