Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02644681
Other study ID # NIMAS/32/OSR
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 2016
Est. completion date March 2018

Study information

Verified date May 2019
Source Scientific Institute San Raffaele
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The primary objective of this study is to evaluate if the motor-evoked potentials/motor action potential amplitude ratio and motor action potential amplitude measurement are useful in detecting spinal cord ischemia during thoracoabdominal aortic aneurysms surgery.

The secondary objective is to evaluate the presence of a correlation between neurophysiological changes and other factors (such as surgical maneuvers, anesthetic and physiologic changes) in order to find which factor is the most important in determining spinal cord ischemia.

This study is an observational, single-center, prospective study on patients with thoracoabdominal aortic aneurysms undergoing surgical repair with intraoperative motor-evoked potentials and somatosensory evoked potentials monitoring.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date March 2018
Est. primary completion date March 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- satisfied criteria for Intraoperative neurophysiological monitoring;

- sign a written informed consent to participate in the study.

Exclusion Criteria:

- No exclusion criteria

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Aortic Aneurysm, Thoracic surgery


Locations

Country Name City State
Italy San Raffaele Hospital Milano

Sponsors (1)

Lead Sponsor Collaborator
Scientific Institute San Raffaele

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of the motor-evoked potentials/motor action potential amplitude ratio The goal of this study is to evaluate the efficacy of different neurophysiological parameters in predicting patient outcome. In particular, our objective is to verify if a better identification of peripheral nerve ischemia during TAAA procedure can improve the sensibility of Intraoperative neurophysiological monitoring in detecting spinal cord ischemia and predicting clinical outcome.
Exploratory univariate analyses will be performed using logistic regression to calculate odds ratios to evaluate neurophysiological parameters associated with poor outcome. Factors that will be found to be significant at p < 0.05 will be then examined in subsequent multivariate analyses to determine significant independent predictors of poor outcome.
During thoracoabdominal aortic aneurysms surgery
See also
  Status Clinical Trial Phase
Active, not recruiting NCT02777593 - Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 2 N/A
Completed NCT02876263 - Noninvasive Neuromonitoring of Surgery of the Thoracic Aorta N/A
Terminated NCT02538822 - Risk of Rupture of Aneurysms of the Thoracic Ascending Aorta (ATA) From the Dynamic Imaging N/A
Completed NCT04930172 - TOtal tRansfemoral branCHed endovasCular tHoracoabdominal Aortic Repair Registry
Completed NCT03207568 - RE-GENERATION: The Safety and Performance of the Relay Pro and Relay NBS Pro Stent-graft Devices in the European Union (EU) N/A
Recruiting NCT03010514 - A Registry Study on Genetics and Biomarkers of Thoracic Aortic Aneurysm/Dissection N/A
Completed NCT02266342 - GORE® TAG® Thoracic Endoprosthesis French Mandatory Registry
Completed NCT00757003 - To Evaluate the Safety and Efficacy for GORE TAG Thoracic Endoprosthesis in the Treatment of Thoracic Aortic Disease Phase 3
Recruiting NCT03574311 - Preoperative Intravenous Ferric Carboxymaltose and Placebo in the Treatment of Patients Undergoing Cardiac Surgery Phase 4
Suspended NCT03410420 - Detection of Hypoxia in Human Thoracic Aorta Using Pimonidazole Hydrochloride Phase 1
Recruiting NCT05703893 - Investigation of the Neurovegetative Pattern in Patients With Thoracic Aortic Aneurysms (TAA)
Enrolling by invitation NCT05800743 - Evaluation of the GORE® Ascending Stent Graft N/A
Completed NCT02253082 - Vasculopathic Injury and Plasma as Endothelial Rescue - OCTAplas Trial (EudraCT no. 2014-000452-28) Phase 4
Recruiting NCT02323581 - Endovascular Treatment of TAAA and Aortic Arch Aneurysms Using Fenestrated and Branched Stent Grafts N/A
Active, not recruiting NCT03414866 - Thoraflex Hybrid Post-Market Study
Recruiting NCT01985906 - Safety and Efficacy of Multiple Overlapping Uncovered Stents for Pararenal Aortic Aneurysm Repair N/A
Active, not recruiting NCT02818972 - RelayPro Thoracic Stent-Graft in Subjects With Thoracic Aortic Aneurysms and Penetrating Atherosclerotic Ulcers N/A
Completed NCT03479164 - Development of Ultra-Low Dose CT Based Screening for Aortic Aneurysms N/A
Completed NCT01775046 - Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment of Descending Thoracic Aortic Diseases (VALIANT CAPTIVIA France)
Recruiting NCT04814238 - Minimally Invasive Aortic Root and Aorta surGery rEgistry