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Investigation of the Effectiveness of Lung Ultrasonography in Intraoperative Fluid Management

Investigation of the Effectiveness of Lung Ultrasonography in the Management of Intraoperative Fluid Therapy, Prospective Observational Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06965634
Enrollment
50
Registered
2025-05-11
Start date
2025-05-20
Completion date
2026-05-30
Last updated
2025-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intraoperative Fluid Management

Brief summary

Adequate and balanced fluid resuscitation is one of the cornerstones of intraoperative patient management. Over-resuscitation leading to positive fluid balance is associated with increased postoperative mortality and morbidity. Invasive and non-invasive technologies can be used for the adequacy of intraoperative fluid therapy. Lung ultrasonography (LUS) is a safe and accurate bedside imaging method. LUS, which is frequently used in the diagnosis of postoperative hypoxemia, has also begun to be preferred for fluid management in intensive care units.

Detailed description

In this study, we aimed to investigate the effectiveness of intraoperative LUS data in the control of fluid therapy.

Interventions

DEVICELung ultrasound

Lung ultrasonography ; lung ultrasonography will be applied in 4 quadrants according to the LUS protocol and LUS score will be created.

Sponsors

Korgün Ökmen
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with surgery with laparotomy

Exclusion criteria

* Chronic obstructive pulmonary disease * Passed lung operation * Uncontrolled hypertension * Acute or chronic kidney failure

Design outcomes

Primary

MeasureTime frameDescription
LUSperoperativeLung ultrasound score (LUS) Lung ultrasonography; Lung ultrasound score will be created by performing ultrasonography in 4 quadrants according to the previously defined protocol. 0 points indicated the presence of only A lines, less than 2 B lines 1. point indicated 1-2 B lines 2. points indicated the presence of more than 3 well-spaced B lines; 3. points indicated the presence of combined B lines

Secondary

MeasureTime frameDescription
CVPperoperativeCentral venous pressure(CVP) Pressure values measured by a central venous catheter applied by jugular or subclavian route
postoperative pulmonary complicationpostoperative 6th hourhypoxia (partial oxygen pressure below 95 on pulse oximetry and 10% decrease from the initial value) atelectasis
biochemical data 1postoperative 6th hourglomerular filtration rate (GFR) values normal results range from 90 to 120 mL/min/1.73 m2.
biochemical data 2postoperative 6th hourBlood urea nitrogen value mg/dl
PVIperoperativePulse variable index (PVI) will be measured by finger pulse oximetry with the MASİMO device.
Mechanical ventilation data 1peroperativeEnd-Tidal Carbon Dioxide Pressure mm/hg The partial pressure of CO2 detected at the end of exhalation is between 35 and 45 mm Hg or 4.0 to 5.7 kPa.
Mechanical ventilation data 2peroperativePeak inspiratory pressure Values Peak inspiratory pressure is the highest pressure applied to the lungs during inhalation and should be kept below 35 cmH2O.It is automatically measured by respirators.
Mechanical ventilation data 3peroperativeTidal Volume value Tidal volume is the volume of gas moving into and out of the lungs with each breath. Normal tidal volume is 6 to 8 mL/kg, regardless of age. It is automatically measured by respirators.
biochemical data 3postoperative 6th hourBlood creatinine value mmol/dl

Contacts

Primary ContactKorgün Ökmen, PhD.
korgunokmen@gmail.com05057081021

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026