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New treatment option for Intraoperative Hypotension
Official title Non-invasive Measurement of the Hypotension Prediction Index for the Reduction of Intraoperative Hypotension
ClinicalTrials.gov ID: NCT06291714
What this study is testing
- What it's testing
- In order to reduce the incidence of IOH, various goal-directed therapy (GDT) protocols have already been introduced with success regarding the reduction of postoperative AKI and MINS. However, these studies used an invasive hemodynamic monitoring which offered a continuous surveillance of the blood pressure.
- 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 45 and older
You may be able to join if
- Patients undergoing major trauma or orthopedic surgery in supine position, which is defined as:
- Reconstructive Surgery of the pelvis (e.g., stabilization of fractures)
- Total hip arthroplasty
- Surgery of the proximal femur (e.g., stabilization of fractures)
- Total knee arthroplasty
You likely can't join if
- \- Predefined exclusion criteria are:
- Planned invasive blood pressure monitoring
- Participation in another treatment study
- Pregnancy and nursing mothers
- Surgery without controlled mechanical ventilation
- ASA I or IV
See the full eligibility criteria
- Patients undergoing major trauma or orthopedic surgery in supine position, which is defined as:
- Reconstructive Surgery of the pelvis (e.g., stabilization of fractures)
- Total hip arthroplasty
- Surgery of the proximal femur (e.g., stabilization of fractures)
- Total knee arthroplasty
- Surgery of the spine
- Performance of general anesthesia with planned duration of \>90min
- Age ≥ 45 years
- \- Predefined exclusion criteria are:
- Planned invasive blood pressure monitoring
- Participation in another treatment study
- Pregnancy and nursing mothers
- Surgery without controlled mechanical ventilation
- ASA I or IV
- Arterial Fibrillation
- Allergy against gelantine
The study team makes the final eligibility decision.
Where it's taking place
- Giessen, Germany
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, 45 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Giessen, Germany. 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.