ClinicalTrials.Veeva

Menu

BNP and Vascular Surgery (BNPinVasc)

U

University of Parma

Status

Unknown

Conditions

Natriuretic Peptide, Brain
Preoperative Period
General Anesthesia
Postoperative Period
Abdominal Aortic Aneurysm
Mets
Vascular Surgery

Study type

Observational

Funder types

Other

Identifiers

NCT03926104
39751 del 19/10/2018

Details and patient eligibility

About

Background and rationale of the study:

Patients undergoing non-cardiac major surgery show a perioperative cardiac risk and postoperative complications, that can be stratified based on parameters linked to patient's conditions and to surgery types.

An accurate identification of this risk could offer numerous advantages for these patients, who's 30-day mortality is around 2%. The identification of the correct risk could lead to a better pre- and postoperative management, that could guarantee a better surgery outcome and a faster postoperative recovery.

To this day there is no perfect method to correctly estimate this risk. Various studies show that high BNP levels are linked to cardiac events at 30 and 180 days. Further investigations identify different groups, at low, intermediate and high risk, based on BNP levels.

BNP is released by ventricular myocytes in response to a wall distress, due to an increased volume, pressure or myocardial ischemia.

So BNP plasma levels could be used as a prognostic and diagnostic marker, improving the cardiac risk stratification in patients undergoing surgery and a much more precise management.

This study is determined to do an evaluation of the correlations between pre- and postoperative BNP levels and the incidence of cardiac events in patients undergoing major vascular surgery.

Full description

Patient's informed consent signature for adhesion at the study will be initially requested. With their acceptance, parameters will be recorded anonymously in the Case Report Form, identified by their initials and a numeric code, until hospital discharge.

The parameters analyzed will be related to:

  • preoperative evaluation: anamnesis, health general conditions, METs, preoperative monitoring, in particularly BNP basal levels;
  • intraoperative evaluation: intraoperative monitoring;
  • postoperative evaluation: BNP and cTnI levels at 24 and 48 hours, and about pulmonary, cardiovascular, neurological and surgical postoperative complications, based on the medical record.

The data will be transferred on Excel worksheet, utilized for descriptive analysis related at every variable.

Enrollment

165 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Ability to provide an informed consent
  • Age >18 years old
  • Elective abdominal aortic aneurysm surgery

Exclusion criteria

  • Emergency surgery
  • Age ˂ 18 years old
  • Creatinine >2mg/dl
  • Diseases of ascending aorta, aortic arch or thoracic aorta
  • Chronic atrial fibrillation
  • Patient refusal to provide informed consent

Trial contacts and locations

1

Loading...

Central trial contact

Elena Giovanna Bignami, MD Professor

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems