Our Anesthesia Experience During MRI Scan

Intracranial Aneurysm Clinical Trial

Official title:

Our Anesthesia Experience During MRI Scan

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03123302
• Other study ID #: MEDAH
• Status: Completed
• Start date: February 1, 2017
• Est. completion date: February 8, 2018

Study information

• Verified date: June 2020
• Source: Akdeniz University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

In this study we aim to investigate the relationship between our anesthesia practice and post procedure complications after MRI scanning with sedation. This is a retrospective, single center observational study. All patients undergoing MRI scan during the study period will be included.

Description:

In this study we aim to investigate the influence of patient characteristics and anesthesia choice on possible complications in patients undergoing MRI under sedation retrospectively.

After one of the routine sedation protocol used in our department was chosen and applied according to the physical status of the patient and the physicians decision, the datas of the patients will be recruited to the study from the medical records . Patient characteristics (age, gender, weight, height), ASA (American Society of Anethesiology) classification, associated diseases will be recorded . After the procedure was completed all the complications during the 2 hours waiting period in the recovery room will be recorded from the medical records. All the complşcation and recovery times will be recorded from the medical records. Whether the patient received radiocontrast material or not will also be recorded. The patients will be called by phone, and will be questioned for the complications, any epileptic seizure attack, or increase in the number of seizures, any admission to emergency room or any in patient admission to the hospital will be recorded which developed in the first week after the procedure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 977
• Est. completion date: February 8, 2018
• Est. primary completion date: February 1, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:All patients undergoing MRI scan wth sedation anesthesia and giving written informed consent.

Exclusion Criteria: patients refusal to be studied.

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Related Conditions & MeSH terms

• Aneurysm
• Epilepsy
• Epileptic Seizure
• Intracranial Aneurysm
• Intracranial Hypertension
• Intracranial Tumor
• Seizures
• Vertebra; Anomaly

Locations

Country	Name	City	State
Turkey	AkdenizU	Antalya

Sponsors (1)

Lead Sponsor	Collaborator
Akdeniz University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Patient characteristics anesthesia choice and possible complications during MRI anesthesia.	To investigate the influence of patient characteristics and anesthesia choice on possible complications of sedation anesthesia during MRI scanning	1 week