Appropriateness of Hemostatic Agent Use in Cardiovascular Surgery
Official title: Evaluation of Appropriateness in the Use of Hemostatic Agents in Cardiovascular Surgery: A Mixed-Methods Single-Center Observational Study
Run by University of Milan · NCT07699016 · Data updated 2026-11-12
This study tests how well surgeons’ choices about topical hemostatic agents match current guidelines in cardiac and vascular surgery at one Milan hospital.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 15 (estimated) |
| Sponsor | University of Milan Academic / other |
| Locations | 1 site (Milan, MI) |
| Status | Recruiting |
| Started | July 1, 2026 |
| Main results expected | July 16, 2026 |
| Study ends | August 15, 2026 |
| Registry record updated | July 13, 2026 |
| Trial ID | NCT07699016 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal participants are attending surgeons, consulting surgeons, and surgical residents actively involved in cardiovascular operations at IRCCS Galeazzi-Sant'Ambrogio Hospital.
✕Probably not a fit
Non-surgical staff or surgeons not currently engaged in cardiovascular operative care may not benefit from the study findings.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
HAEMOVAX is a single-center mixed-methods observational study that combines an anonymous survey of cardiovascular surgeons with a retrospective audit of how hemostatic agents are used. It uses standardized clinical vignettes based on EACTS and ESA recommendations to measure Knowledge-Practice Alignment (KPA-Score). The study aims to understand real-world usage patterns, barriers to appropriate use, and how declared knowledge aligns with actual decision-making. Results could reveal variability in practice, inform resource allocation, and identify gaps between guidelines and routine care.
Why it matters
Potential benefit: If successful, the study could improve adherence to guidelines and reduce unnecessary use and costs of topical hemostatic agents.
How similar studies have gone: Previous research on hemostatic agent use has shown variability and gaps between guidelines and practice; this study applies a structured, real-world assessment in a single center.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Physicians with a surgical role in the Departments of Cardiac Surgery or Vascular Surgery at IRCCS Galeazzi-Sant'Ambrogio, Milan Including attending surgeons, consultant surgeons, and surgical residents * Active participation in cardiovascular operative procedures during the study period (or within the preceding 12 months) * Employment at the study institution at the time of survey administration Willingness to participate and complete the anonymous structured questionnaire Exclusion Criteria: * Non-surgical healthcare personnel (e.g., nurses, anesthesiologists, administrative staff, or allied health professionals) * Surgeons not involved in operative cardiovascular practice during the study period * External collaborators or visiting surgeons without regular clinical activity at the institution * Individuals who do not provide informed consent for participation in the anonymous survey * Questionnaires with missing or incomplete vignette responses preventing calculation of the KPA-Score
Where it's running
-
IRCCS Galeazzi Sant'Ambrogio Hospital
Milan, Mi, Italy Recruiting
Study contacts
- Study coordinator: Luca Galassi, MD
- Email: luca.galassi@unimi.it
- Phone: +393458013083
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Impact of Fast-Track Anesthesia on Postoperative Delirium After Cardiac Surgery
This observational study tests whether fast-track anesthesia, compared with conventional care, is linked to lower rates of delirium after elective cardiac surgery in adults.
-
Sarcopenia in Patients After Cardiac Surgery
This observational study tests how common sarcopenia is after cardiac surgery and whether current care helps improve muscle mass and function.
-
NasoAid vs NasoPore after Nasal Surgery
This study tests whether collagen-based NasoAid® nasal packing works as well as the synthetic NasoPore for stopping bleeding after nasal surgery in adults.
-
Preoperative functional optimization for adults undergoing major cardiac or abdominal surgery
This study tests a four‑week prehabilitation program to improve fitness before elective major cardiac or abdominal surgery.
-
Biomarkers to predict CSA-AKI risk before heart surgery
This study tests new biomarkers to see if they can predict CSA-AKI risk in adults undergoing cardiovascular surgery.
-
Bleeding control after single-ray amputation: Hemocoll vs Avitene vs bone wax
This trial tests whether Hemocoll, Avitene, or bone wax better stop bleeding from exposed bone after a planned single-ray amputation in adults.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.