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Pulmonary Edema - AcuteNCT06820112

Comparison of Respiratory Support for Acute Pulmonary Edema

An observational study of Pulmonary Edema - Acute, run by The First Affiliated Hospital of Guangzhou Medical University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This study is a retrospective study. The demographic and vital signs of patients with acute pulmonary edema are retrospectively collected to compare the prognosis of patients after receiving different respiratory support. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Pulmonary Edema - Acute
What is being tested?
mechanical ventilation
How many people
200 participants
Where
No sites listed yet
Study dates
6 Feb 2025to 1 Apr 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients diagnosed with acute pulmonary edema

Who may be able to join

  • diagnosis of acute pulmonary edema

Who cannot join

  • Under 18 years old

Trial locations and contacts

No sites are listed yet.

About this study

Official title: This Study Retrospectively Collected Relevant Patient Data to Compare the Effects of Different Respiratory Support Modalities in Patients With Acute Pulmonary Edema.

This study is a retrospective study. The demographic and vital signs of patients with acute pulmonary edema are retrospectively collected to compare the prognosis of patients after receiving different respiratory support.

Being tested
mechanical ventilation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • mechanical ventilationOther

    patients who received mechanical ventilation

Study groups in NCT06820112
Study groupRoleWhat they receive
oxygen therapyNot described
Receives: Other: mechanical ventilation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. death rate

    Measured: 28 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Feb 2025
  2. Study start6 Feb 2025 (estimated)
  3. Primary completion20 Mar 2025 (estimated)
  4. Study completion1 Apr 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Retrospective
Enrolment
200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06820112
Sponsor's protocol ID
20252502
Status last verified
Oct 2024
First submitted
6 Feb 2025
Last updated
11 Feb 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Pulmonary Edema - Acute, run by The First Affiliated Hospital of Guangzhou Medical University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 11 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Huang (81566675, huangqiaoyun23@foxmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

death rate (time frame: 28 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Feb 2025.

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