Recruiting NA Postoperative Pulmonary Complications (PPCs)

New treatment option for Postoperative Pulmonary Complications (PPCs)

Official title PROtective Ventilation With FLOW-Controlled Ventilation

ClinicalTrials.gov ID: NCT06703814

What this study is testing

What it's testing
The investigators want to investigate in patients undergoing robot-assisted laparoscopic surgery (a minimally invasive procedure) how applicable flow-controlled ventilation is, and whether it might also be safer than the current ventilation techniques, as well as its impact on potentially reducing the risk of lung-specific complications. Flow-controlled ventilation has already been tested in several studies on animals and humans and has proven to be a safe form of ventilation for patients undergoing surgery under general anesthesia.
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older. Healthy volunteers may be eligible.

You may be able to join if

  • undergoing elective robot-assisted laparoscopic surgery in supine or Trendelenburg position (either abdominal, urologic or gynecologic surgery);
  • AND increased risk of PPCs according to the ARISCAT risk score (≥ 26 points);
  • OR the combination of age \> 40 years, scheduled surgery lasting \> 2 hours and planned to receive an intra-arterial catheter for blood pressure...
  • aged ≥ 18 years; and
  • able to give written informed consent to participate in the study and agree to comply with the study protocol prior to initiation of any...

You likely can't join if

  • ideal body weight \< 40 kg;
  • ASA Physical Status Classification System score IV - VI;
  • previous enrolment into the current study;
  • being the study investigator, his/her family members, employees and other dependent persons;
  • if female and of childbearing potential, known pregnancy or a positive urine pregnancy test (confirmed by a positive serum pregnancy test), or...
  • No informed consent

The study team makes the final eligibility decision.

Where it's taking place

  • Innsbruck, Tyrol, Austria
  • Bochum, Germany, Germany
  • Sankt Gallen, Canton of St. Gallen, Switzerland

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Innsbruck, Tyrol, Austria; Bochum, Germany, Germany; Sankt Gallen, Canton of St. Gallen, Switzerland. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.