A Comparative Study of Different Hypothermic Circulatory Arrest Strategies on Aortic Surgery.

NCT03454633 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2018-08-06

No results posted yet for this study

Summary

By comparing the clinical outcome of patients underwent different hypothermic circulatory arrest (mild hypothermic versus moderate hypothermic) during aortic arch surgery, this study aims to determine the optimal hypothermic circulatory arrest strategy for aortic surgery.

Conditions

  • Morality
  • Hypothermic Circulatory Arrest Time
  • Aortic-cross Clamping Time
  • Cardiopulmonary Bypass Time
  • Operation Time
  • Re-Thoracotomy
  • ICU Stay
  • Mechanical Ventilation Time
  • Blood Transfusion
  • Neurological Disorder
  • Dialysis
  • Aneurysm
  • Endoleak
  • Hospital Stay

Interventions

PROCEDURE

the temperature of hypothermic circulatory arrest

Different temperature (mild 30 degree or moderate 25 degree) employed during the hypothermic circulatory arrest on aortic surgery.

Sponsors & Collaborators

  • Jie He.MD

    collaborator UNKNOWN
  • Shihao Cai.MD

    collaborator UNKNOWN
  • Wenda Gu.PhD

    collaborator UNKNOWN
  • Haijiang Guo.PhD

    collaborator UNKNOWN
  • Liang Hong. MD

    collaborator UNKNOWN
  • Ruixing Fan.PhD

    collaborator UNKNOWN
  • Jingsong Huang.PhD

    collaborator UNKNOWN
  • Tucheng Sun.MD

    collaborator UNKNOWN
  • Jihai Peng.MD

    collaborator UNKNOWN
  • Xiaoping Fan. MD

    lead OTHER

Principal Investigators

  • Xiaoping Fan, PhD · Guangdong General Hosiptal

  • Jie He, MD · Guangdong General Hosiptal

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-03
Primary Completion
2020-02-15
Completion
2020-12-15

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03454633 on ClinicalTrials.gov