Vascular Surgical Procedure

4

Review clinical trials related to Vascular Surgical Procedure. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Opioid Free Anesthesia-Analgesia Strategy and Surgical Stress in Elective Open Abdominal Aortic Aneurysm Repair

Open Abdominal Aortic Aneurysm (AAA) repair is a high-risk surgical procedure accompanied by intense endocrine and metabolic responses to surgical stress, with subsequent activation of the inflammatory cascade, cytokine and acute-phase protein release, and bone marrow activation. There is a proven correlation of surgical stress, which patients undergoing open AAA repair are subjected to, with patient outcome, morbidity/mortality, intensive care unit stay and overall length of stay. Modern general anesthetic techniques have been revised and rely on perioperative multimodal anesthetic and analgesic strategies for improved overall patient outcome. Based on this context of a multimodal anesthetic technique and having taken into consideration the international "opioid-crisis" epidemic, an Opioid Free Anesthesia-Analgesia (OFA-A) strategy started to emerge. It is based on the administration of a variety of anesthetic/analgesic agents with different mechanisms of action, including immunomodulating and anti-inflammatory effects. Our basic hypothesis is that the implementation of a perioperative multimodal OFA-A strategy, involving the administration of pregabalin, ketamine, dexmedetomidine, lidocaine, dexamethasone, dexketoprofen, paracetamol and magnesium sulphate, will lead to attenuation of surgical stress response compared to a conventional Opioid-Based Anesthesia-Analgesia (OBA-A) strategy. Furthermore, the anticipated attenuation of the inflammatory response, is pressumed to be associated with equal or improved analgesia, compared to a perioperative OBA-A technique.

Participants needed: 40
Trial details
Phase: Phase 4Age: 40-85Biological sex: AllType: InterventionalSponsor: University of CreteUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Patient Consent [+2]

Immunocompromised patients [+7]

Status: Recruiting

Measurement Of NT-proBNP to Predict Outcomes in Surgery

The team is investigating whether N-terminal pro B-type natriuretic peptide (NT-proBNP) and other cardiac markers are useful for predicting outcomes for patients undergoing vascular surgery. By measuring NT-proBNP before and after surgery, the investigators may be able to determine which patients are at risk of an adverse outcome, such as a heart attack or death.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Norfolk and Norwich University Hospitals NHS Foundation TrustUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

Patients who are equal to or over 18 years old [+10]

Patients undergoing emergency surgery [+4]

Status: Not yet recruiting

Lymphatic Injury Visualization in Vascular Surgery

This study aims to assess a simple intervention: Visualization of lymphatic injury + treatment (in case of detection). This will generate data on the incidence of intraoperative lymphatic injury and the effect of treatment. This data will then hopefully enable a multi-center RCT to generate high level evidence on this matter.

Participants needed: 60
Trial details
Age: 18-100Biological sex: AllType: InterventionalSponsor: University Hospital, Basel, SwitzerlandUpdated: Mar 30, 2026Locations: 1
Eligibility criteria

adult patients undergoing vascular surgery procedures in the groin [+1]

pregnant or lactating women [+4]

Status: Recruiting

Leica Microsystems Sponsored Study to Collect and Confirm Clinical Data on the Performance of the GLOW800 Device When Used in Accordance With Its Intended Use.

This post-market clinical follow-up (PMCF) study aims to confirm the safety and performance of the GLOW800 surgical microscope accessory when used in conjunction with the ARveo8x surgical microscope. The study evaluates fluorescence visualization and image quality during standard surgical procedures in the cerebral vascular area and plastic and reconstructive surgery. It is a non-interventional, observational study conducted in routine care settings across multiple European sites.

Participants needed: 29
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Leica Microsystems (Schweiz) AGUpdated: Jan 20, 2026Locations: 3
Eligibility criteria

Participants must be 18 years of age or older at the time of signing the informe... [+3]

Known allergy to Indocyanine Green (ICG) cyanine dye. [+3]