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Could belly pressure predict heart surgery outcomes?

NCT ID NCT07752082

Knowledge-focused Sponsor: Bursa Yuksek Ihtisas Training and Research Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 07, 2026 · Last updated Aug 07, 2026

Summary

This study looks at whether increased pressure inside the abdomen, measured after open-heart surgery, is linked to a higher risk of complications or death. Researchers will measure this pressure in 100 adults at three key times during and after surgery. They will then compare recovery outcomes, such as time on a breathing tube, hospital stay, and complications, between patients with high and normal pressure. No treatment is given; the goal is simply to see if this measurement could help predict who needs extra care.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If a link is found, it could lead to better monitoring and early intervention to reduce complications after open-heart surgery.
What could go wrong
This is an observational study, so it can only show associations, not cause and effect. Results may be influenced by other factors and may not apply to all patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

100 people

The number who actually took part.

Started

Mar 2023

Finished

Mar 2024

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population consisted of consecutive adult patients scheduled for elective open-heart surgery with cardiopulmonary bypass at the Department of Anesthesiology and Reanimation of Bursa Yüksek İhtisas Training and Research Hospital between March 2023 and March 2024. Eligible patients who provided written informed consent were enrolled prospectively. Participants were classified according to whether intra-abdominal hypertension developed during the perioperative period. A total of 100 patients were enrolled, and 98 patients were included in the final comparative analysis.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age 18 years or older * Scheduled for elective open-heart surgery using cardiopulmonary bypass * Left ventricular ejection fraction of 40% or higher * Provision of written informed consent Exclusion Criteria: * Age under 18 years * Requirement for emergency cardiac surgery * Open-heart surgery performed without cardiopulmonary bypass * Body mass index of 35 kg/m² or higher * Uncontrolled diabetes mellitus * History of urinary bladder or urinary tract surgery * Active urinary tract infection * Acute or chronic renal failure * Neurogenic bladder * History or presence of cerebrovascular disease

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Conditions

The condition(s) this trial relates to.

Intra-Abdominal Hypertension Postoperative Complications

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Intra-abdominal hypertension Postoperative complications

Contacts and locations

Locations

  • Bursa Yuksek Ihtisas Research and Education Hospital

    Bursa, Yıldırım, 16310, Turkey (Türkiye)

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