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Not yet recruitingNCT05439811Updated Jul 6, 2022

Retrospective Data Analysis on the Application of Swan-Ganz Catheter in Cardiac Surgery

An observational study in Postoperative Complications, sponsored by Huazhong University of Science and Technology. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-07-06.

Sponsored by Huazhong University of Science and Technology · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2025, 1 year 3 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
3,000
Ages
18 Years and older
Sex
All
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Study summary

The investigators aimed to investigate postoperative complications associated with Swan-Ganz Catheter based on the clinical data of Wuhan Union Hospital and Wuhan Asian heart hospital for 10 years, including major cardiovascular, respiratory adverse events, ICU time, mechanical ventilation time, length of hospital stay, in-hospital mortality, and 30-day postoperative mortality events.

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Conditions studied

  • Postoperative Complications

Keywords

  • Swan-Ganz Catheter
  • Cardiac Surgery
  • Postoperative complications
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In context

Postoperative Complications

1,235 studies on the registry are indexed under Postoperative Complications; 294 are open to participants now.

This study's planned enrollment of 3,000 is above the median of 253 across 521 observational studies indexed under Postoperative Complications.

Browse Postoperative Complications studies →

Lead sponsor

Huazhong University of Science and Technology is the lead sponsor of 242 studies on the registry; 61 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Probability sample

Study population

Adults undergoing cardiac surgery

Inclusion criteria

  • Over 18 years old;
  • Patients undergoing major cardiac surgery under general anesthesia;
  • Patients with complete sex, age, use of floating catheter and prognosis data

Exclusion criteria

Exclusion Criteria:

  • ASA grade V and above;
  • End stage renal disease requiring (or undergoing) renal replacement therapy;
  • Pregnant or lactating women
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Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
3,000 participants (estimated)
Patient registry
No

Interventions

  • ProcedureSwan-Ganz Catheter

    Swan-Ganz Catheter

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What researchers measure

Primary outcomes

  1. Number of participants with cardiovascular events

    1) Cardiac death; 2) Non fatal myocardial infarction; 3) Intra aortic balloon counterpulsation (IABP); 4) Thoracotomy exploration; 5) Heart failure.

    Time frame: one week after operation

  2. Number of participants respiratory adverse events

    1) Acute lung injury: Diagnosis according to Berlin diagnostic standard; 2) Atelectasis: X-ray confirmed with body temperature \>37.5c or abnormal pulmonary manifestations; 3) Pneumothorax: chest X-ray diagnosis; 4) Pneumonia: confirmed by radiology or bacteriology

    Time frame: one week after operation

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Undecided — If the patient's privacy information is not involved, you can contact the research team by email to obtain data (yaoshanglong@hust.edu.cn)

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 6, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05439811
Lead sponsor
Huazhong University of Science and Technology
Collaborators
Wuhan Asia Heart Hospital
Responsible party
Shanglong Yao (Clinical Professor, Wuhan Union Hospital, China) — Principal investigator
First posted
Jun 30, 2022
Start date
Jun 30, 2022 (estimated)
Primary completion
Jun 30, 2025 (estimated)
Completion
Dec 30, 2025 (estimated)
Last update
Jul 6, 2022
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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