🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in Turkey / NCT07766967
Starting soon Not applicable

Alveolar Recruitment Maneuver-Induced Hypotension: A Dynamic Consequence and Intraoperative Indicator of Fluid Responsiveness

NCT07766967 · tracked via the Priya Life Science Turkey tracker
Sponsor
University of Health Sciences Balikesir Hospital Eduation and Research
Phase
Not applicable
Started
2026-07-15
Last updated
2026-08-17

Condition(s) studied

Hypotension Drug-InducedGeneral Anesthesia Using Endotracheal IntubationAtelectasisFluid ResponsivenessMechanical Ventilation

Investigational drug(s) / intervention(s)

Alveolar Recruitment Maneuver (ARM)Passive Leg Raising (PLR) Test

Alveolar Recruitment Maneuver (ARM): ARM is performed using a stepwise increase in positive end-expiratory pressure (PEEP) in pressure-controlled ventilation mode until peak inspiratory pressure reaches 40 cmH₂O, then stepwise decrease back to baseline. Hemodynamic parameters are continuously monitored throughout the maneuver.

Passive Leg Raising (PLR) Test: With the patient in supine position under general anesthesia, both legs are raised to 45 degrees for 60 seconds. The change in mean arterial pressure (ΔMAP) is recorded as an indicator of preload responsiveness. The test is performed immediately before each ARM.

Study summary

This study investigates whether two simple bedside tests - the Passive Leg Raising (PLR) test and the Pleth Variability Index (PVI) - can predict a drop in blood pressure that sometimes occurs during a lung-opening procedure called an Alveolar Recruitment Maneuver (ARM).

ARM is routinely performed during general anesthesia to prevent lung collapse and improve oxygen levels. However, in some patients - particularly those with low fluid levels - ARM can cause a temporary but significant drop in blood pressure (hypotension), which may require immediate treatment.

In this prospective observational study, adult patients scheduled for elective non-cardiac, non-thoracic surgery under general anesthesia will be enrolled. Before each ARM is performed, PLR test and PVI values will be measured. We will then evaluate how well these measurements predict whether the patient will develop ARM-induced hypotension.

If PLR and PVI can reliably identify patients at risk, clinicians may be able to take preventive steps before performing ARM, making the procedure safer for vulnerable patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:Age 18 years or older ASA physical status I or II Scheduled for elective non-cardiac, non-thoracic surgery under general anesthesia Able to provide written informed consent - Exclusion Criteria:Cardiac or thoracic surgery Hemodynamic instability at baseline (MAP \<65 mmHg or requirement for vasopressors) Severe valvular heart disease or known cardiac dysfunction (EF \<40%) Chronic obstructive pulmonary disease (COPD) or severe respiratory disease Atrial fibrillation or other significant arrhythmias Peripheral vascular disease affecting PVI signal quality Body mass index (BMI) \>40 kg/m² Emergency surgery Refusal to participate or inability to provide informed consent Pregnancy \-

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Balıkesir Atatürk City Hospital Balıkesir Altıeylül

More University of Health Sciences Balikesir Hospital Eduation and Research trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07766967 on ClinicalTrials.gov ↗ ← All trials in Turkey