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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05409469
Other study ID # NanjingFirst AAD
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2012
Est. completion date December 2021

Study information

Verified date May 2022
Source Nanjing First Hospital, Nanjing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This study constructed a retrospective cohort study by retrospectively analyzing the data of all patients with aortic dissection from January 1, 2012 to December 31, 2021 from the Cardiovascular Disease Registration System of Jiangsu Province in China and the data of similar diseases in recent years from National Inpatient Sample database in the United States


Recruitment information / eligibility

Status Completed
Enrollment 11550
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1.Clinical diagnosis of type A Aortic Dissection Exclusion Criteria: 1. age<18, age unknown, 2. diagnosis of aortic aneurysm, transfer out within 1 day, 3. unknown vital status at discharge; 4. unknown treatment type: cardioplegia, valve or cardiac repair only without aortic repair or two types of treatments on different days

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
surgery
surgery on patients with aortic dissection

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Xin Chen China Medical University, China

Outcome

Type Measure Description Time frame Safety issue
Primary Baseline data of patients with type A aortic dissection was assessed by SPSS 17.0 Baseline data of patients with type A aortic dissection included gender, age,height, weight, past medical history, family history, hospital costs, etc. from 2015 to 2019
Primary The main efficacy indicators was assessed by SPSS 17.0. The main efficacy indicators included surgical procedures, surgical outcome (postoperative bleeding, ICU stay, extubation time), perioperative complications (including infection, bleeding, neurological complications, cardic complications, renal insufficiency, etc.), and postoperative mortality. from 2015 to 2019
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