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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03136536
Other study ID # 206471
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 3, 2017
Est. completion date December 31, 2022

Study information

Verified date March 2021
Source Region Örebro County
Contact Kristofer F Nilsson, MD, PhD
Phone 196020352
Email kristofer-bo-ingemar.nilsson@regionorebrolan.se
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to investigate the mortality and frequency of organ dysfunction in patients after endovascular thoracoabdominal aortic surgery, and to search for biomarkers of organ dysfunction, in particular the spinal cord, the kidneys and the gastrointestinal tract. All adult patients undergoing endovascular thoracoabdominal aortic surgery at Örebro University Hospital, Örebro, Sweden, are asked for participation in this study. All participating patients sign informed consent at the inclusion. During the operation and during the postoperative intensive care, the function of the spinal cord, the gastrointestinal tract and the kidneys are collected along with other clinical parameters. Plasma blood samples, urin samples and cerebrospinal fluid samples are collected from each patient during the operation and during the postoperative care at the intensive care unit. During the operation two microdialysis catheters are placed in the abdomen, and the samples are continuously collected and analyzed. The biomaterial samples are stored in a biobank for later determination of proteins and other molecules. Postoperative survival and the frequency of complications are analysed.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 31, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Accepted for endovascular advanced thoracoabdominal aortic surgical procedure - Adult Exclusion Criteria: - Pregnant

Study Design


Locations

Country Name City State
Sweden Department of Cardio-thoracic and Vascular Surgery, Örebro University Hospital Örebro

Sponsors (1)

Lead Sponsor Collaborator
Region Örebro County

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Other Proteomics Plasma, urine, cerebrospinal fluid, intraperitoneal microdialysate Postoperative: 7 days
Primary Mortality Overall and aortic-related mortality 1 year postoperative
Secondary Organ dysfunction and failure Spinal cord, gastrointestinal tract, kidneys Postoperative: 7 days, 30 days, 1 year follow-up
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