CClinicalTrials.gg
Status unknownNCT03123536Updated Apr 21, 2017

Use of Point-of-care Ultrasound in High Risk Surgical Patients

An observational study in Ultrasonography, Outcomes and Cardiopulmonary, sponsored by Zhongda Hospital. Status unknown at 1 site in China. Per ClinicalTrials.gov, last updated 2017-04-21.

Sponsored by Zhongda Hospital · Observational

The sponsor has not verified this record recently (last verified Apr 2017), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
200
Sex
All
01

Study summary

There is currently a lack of evidence to support the use of perioperative point-of-care ultrasound to assess the outcomes in high risk surgical patients. Thus, the purposes of this study were to evaluate whether perioperative use of point-of-care ultrasound can reduce the worse postoperative outcomes in high surgical patients.

Read the detailed description

Point-of-care ultrasound is increasingly established as a useful bedside tool when performed by the anesthesiologist for evaluation of cardiopulmonary dysfunction and other emergent situations. However, it remains unclear whether use of perioperative point-of-care ultrasound can reduce the worse postoperative outcomes in high surgical risk patients.

Patients were randomly allocated to two groups. In the point-of-care ultrasound group, treatment was oriented by the findings of point-of-care ultrasound, while in the control group the decisions about the management of patients were made by the experience of the clinical team. The primary outcome measures were hospital mortality and 28-day mortality, and the secondary outcome measures were the complications and length of hospital stay.

02

Conditions studied

  • Ultrasonography
  • Outcomes
  • Cardiopulmonary

Keywords

  • high risk
  • complication
  • Ultrasonography
03

In context

Lead sponsor

Zhongda Hospital is the lead sponsor of 101 studies on the registry; 40 are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

More and more high risk patients undergo surgery,which is associated with increased morbidity and mortality. The aim of the present study was to investigate the value of point-of-care ultrasound for assessment of postoperative outcomes in high risk surgical patients.

Inclusion criteria

  • Patients who have comprised cardiovascular,respiratory diseases,or other critical illness.

Exclusion criteria

Exclusion Criteria:

  • Patients who decline to participate.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
200 participants (estimated)
Patient registry
No

Groups and cohorts

  • Point-of-care ultrasound group

    High risk patients received point-of-care ultrasound assessment perioperatively, treatment was oriented by the findings of point-of-care ultrasound.

    Device: Point-of-care Ultrasound

  • Control group

    High risk patients received management by the experience of the clinical team.

Interventions

  • DevicePoint-of-care Ultrasound

    Patients' management in the point-of-care ultrasound group will be adjusted according to the results of ultrasound, whereas patients in the control group the decisions about the management were made by the experience of clinical team.

06

What researchers measure

Primary outcomes

  1. Hypotension

    Patients who have hypotension which is defined by mean arterial pressure less than 60 mmHg

    Time frame: Within 7 days after surgery

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 21, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03123536
Lead sponsor
Zhongda Hospital
Responsible party
Jian-jun Yang (Director, Department of Anesthesiology, Zhongda Hospital) — Principal investigator
First posted
Apr 21, 2017
Start date
Feb 1, 2017
Primary completion
May 2018 (estimated)
Completion
Sep 2018 (estimated)
Last update
Apr 21, 2017

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2017. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion