Skip to content

Effect Alveolar Recruitment Manoeuver on Stroke Volume a Randomized Study

Hemodynamic Effect of Alveolar Recruitment Manoeuver Through Stepwise Increase and Decrease in Irway Pressure or Sustained 30 Secondes 30 cmH2O Continuous Positive Airway Pressure. A Randomized Study.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04802421
Acronym
hemorecrut-2
Enrollment
70
Registered
2021-03-17
Start date
2021-03-12
Completion date
2022-04-01
Last updated
2021-03-17

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

Conditions

Alveolar Recruitment Manoeuver, Anesthesia

Brief summary

Objective: to compare the effect of alveolar recruitment manouver through stepwise increase and decrease in airway pressure or sustained 30 secondes 30 cmH2O continuous positive airway pressure on cardiac stroke volume estimated by oesophageal doppler in preload independent anesthetized patients scheduled for surgery.

Detailed description

Following anesthesia and preload optimisation guided by cardiac stroke volume, patients will be randomised to one alveolr recruitment manoeuver : * stepwise increase and decrease in positive airway pressure * sustained 30 secondes 30 cmH2O continuous positive airway pressure The primary objective is the change in cardiac stroke volume.

Interventions

PROCEDUREalveolar recruitment manoeuver

alveolar recruitment manoeuver are recommended during general anesthesia to prevent pulmonary atelectasis

Sponsors

University Hospital, Caen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Caregiver)

Masking description

The patient will not know the allocation group because he will be anesthetised before randomisation. The care provider (anesthetist) will not know the allocation group because the intervention will be applied by an independent investigator not involved in care of the patient.

Intervention model description

randomised parallel groups. randomisation between 2 groups equilibated by randomised blocks of 4, 6 or 8

Eligibility

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

Inclusion criteria

* adult patients scheduled for major surgery requiring hemodynamic monitoring * written signed informed consent

Exclusion criteria

* pregnancy * non sinusal heart rate * known cardiac right ventricular failure or arterial pulmonary hypertension * pneumothorax * known pulmonary emphysema

Design outcomes

Primary

MeasureTime frameDescription
cardiac stroke volume1 minchange in cardiac stroke volume during the alveolar recruitment manoeuver

Secondary

MeasureTime frameDescription
arterial pressure1 minchange in arterial pressure during the alveolar recruitment manoeuver
recovery at 3 min3 minrecovery of cardiacstroke volume and arterial pressure 3 min after the end of alveolar recruitment manoeuver

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026