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How much IV fluid is too much? lung scans put surgical fluid levels to the test

NCT ID NCT06104020

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 16, 2026 · Last updated Sep 17, 2026 · Updated 1 time

Summary

Researchers at Assiut University are comparing two intravenous fluid strategies during shoulder arthroscopy: a restrictive approach that aims for net zero fluid balance and a liberal approach that gives more fluid. They will use lung ultrasound to look for postoperative pulmonary complications and track blood pressure, heart rate, oxygen levels, and vasopressor use. The trial enrolls 60 adults scheduled for elective shoulder arthroscopy to see which fluid strategy better protects the lungs and keeps circulation stable.

What this could mean

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

Active substance
intraoperative fluid management strategies (restrictive versus liberal intravenous fluids)
What this could lead to
If one fluid approach proves safer, it could shape how anesthesiologists manage IV fluids during shoulder arthroscopy to lower the risk of breathing problems after surgery.
What could go wrong
This is a small single-center study of 60 people, so its results may not apply to other hospitals or patients with different health profiles. Lung ultrasound scores are an indirect measure, and fluid shifts during surgery can be hard to control.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

60 people

The number who actually took part.

Started

Nov 2024

Finished

Dec 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

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: * Patients scheduled for elective shoulder arthroscopic surgery. * Adults aged 18 years and above. * Capable of providing informed consent voluntarily. * No known allergies or sensitivities to substances commonly used in the surgical procedure or study. * Stable baseline hemodynamics during preoperative evaluation Exclusion Criteria: * Patients scheduled for open shoulder surgery. * Medical Comorbidities: * Pulmonary diseases, including chronic pulmonary diseases or pulmonary edema. * Previous cardiac diseases such as heart failure, myocardial infarction (MI), hypertension, and known types of arrhythmia. * Severe Organ Disease: Severe liver or kidney disease. * Body mass index (BMI) ≥ 35 kg/m². * Abnormal coagulation function. * Pregnancy * Refusal to Participate or Patients who cannot provide informed consent due to cognitive impairment or other reasons. * Previous shoulder arthroscopy.

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Assuit university

    Asyut, Egypt