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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02816892
Other study ID # 2XY-ED-002
Secondary ID
Status Recruiting
Phase N/A
First received April 25, 2016
Last updated June 25, 2016
Start date June 2016
Est. completion date December 2016

Study information

Verified date June 2016
Source Central South University
Contact Xiangping Chai, M.D.
Phone +86-13787204259
Email laochaicn@aliyun.com
Is FDA regulated No
Health authority China: National Natural Science Foundation
Study type Observational

Clinical Trial Summary

This study aims to investigate Serum Tenascin C levels in patients with acute symptoms relating to a known or newly diagnosed aortic aneurysm in emergency department and reveals the possible role of Tenascin C in the development of the disease.


Description:

Patients with acute and chronic aortic disease /survivors and non-survivors were compared. Further subgroup analysis on the characteristics of the aneurysm and patients were performed. The aneurysms (ruptured and dissected) were divided according to the style of the Stanford classification,according to the location of the pathology in aneurysms of the ascending thoracic aorta .the descending thoracic aorta, or the abdominal aorta.The subgroup were divided according to the extent of propagation of the disease (rupture,covered rupture, acute dissection, chronic dissection and ectasia). Rupture was defined by direct visualisation of the discontinuity of the aortic wall by computed tomography, sonography, intraoperative findings or at autopsy with detection of blood in the pleural, pericardial or abdominal cavity. Covert rupture was defined as an intramural haematoma without detection of free blood in the body cavities. Acute dissection was defined when blood separating the layers of the aortic media was newly diagnosed. Chronic dissection was defined as the absence of any visible propagation of a known dissection compared to preexisting examinations. Ectatic aneurysm was defined as a permanent localised dilatation of the aorta with a diameter of at least 50% greater than normal. Documentation of the surgical interventions and autopsy reports was used to confirm the diagnosis. In all patients the investigators collected the history, age of the patients, duration of pain, blood pressure at admission and laboratory parameters (haematocrit, creatinine) and Tenascin C Serum levels after admission to our emergency department immediately. The patients were followed up until hospital discharge and the outcome (survived/died) was recorded.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- adults

- sudden severe thoracic or abdominal pain

Exclusion Criteria:

- lesser than 18 years

- pregnant women

- trauma

- tumour

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China The Second Xiangya Hospital of Central South University Changsha Hunan

Sponsors (1)

Lead Sponsor Collaborator
Central South University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The level of serum tenascin-C serum tenascin-C in ng/ml was measured by elasia lesser than 48hours Yes
Secondary Characteristics of enrolled subjects age in years,sex,IBM in kg/m^2 and associated history was collected lesser than 48hours Yes
Secondary The level of D-D,C-reactive protein,elastic protein fragment The level of D-D in ng/ml,C-reactive proteinin ng/ml,elastic protein fragmentin ng/ml was measured by elasia lesser than 48hours Yes
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