Endovascular Procedures

6

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

Condition / disease
Location
Status: Not yet recruiting

Sensorised Surgical Gloves for Neuroendovascular Procedures

A deeper understanding of the forces required for optimal flow diverter stent deployment could improve procedural safety and shorten the learning curve for new devices. In the past, force sensors have been physically attached to devices in some way. The investigators approach is to incorporate force sensors into the hands of the operator handling the device using sensorised surgical gloves. Participants will be asked to deploy a Flow Diverter (FD) in a biorealistic silicone model while wearing force sensing surgical gloves. The primary objective of the study is to show whether sensorised gloves are capable of meaningful force detection in neurointerventional procedures. The investigators will also explore the potential of developing computer vision technology in neurointervention. The investigators are inviting groups of experts and novices to participate. This will allow the investigators to understand if analysis of glove force outputs can distinguish operator experience.

Participants needed: 12
Trial details
Biological sex: AllType: InterventionalSponsor: NHS LothianUpdated: May 6, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Head Cooling in Ischaemic Stroke Patients Undergoing Endovascular Thrombectomy (COOLHEAD-2b)

COOLHEAD-2b is a multicentre, phase 2, prospective, randomised, controlled, open-label, blinded-endpoint trial evaluating the safety and efficacy of non-invasive convective head cooling as an adjunct to endovascular thrombectomy (EVT) in patients with acute anterior circulation ischaemic stroke. Head cooling is initiated as early as possible, including during inter-hospital transfer, and continued until one hour after reperfusion. The primary efficacy endpoint is final infarct volume at 24 hours.

Participants needed: 182
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Auckland City HospitalUpdated: Apr 13, 2026Locations: 1
Eligibility criteria

Acute anterior circulation ischaemic stroke planned for endovascular thrombectom... [+1]

Pre-stroke modified Rankin Scale score >2 [+6]

Status: Recruiting

Introduction of an Operating Room Black Box to Identify, Analyse and Prevent Errors in the Vascular Hybrid Room

The "OR Black box", an inclusive multiport data capturing system has been developed and successfully used for detailed analysis of laparoscopic surgical procedures. A pilot study has shown that this system can be successfully installed in the hybrid room at Ghent University Hospital and used for detailed analysis of intra-operative errors and radiation safety issues in endovascular procedures. Secondary analysis of pilot study data via direct video coding assessed the relationship between leadership style of the surgeon and team behavior and possible fluctuations during surgery. This novel approach allows a prospective objective assessment of human and environmental factors as well as measurement of errors, events and outcomes. In this study, the aim is to use the acquired knowledge to characterize a chain of events, identify high-risk interventions and identify areas for improvement, both on an organizational, team or individual level. Hypothesis: non-technical skills, environmental factors and teamwork in the hybrid room correlate with surgical technical performance and error rates. Furthermore, we hypothesize that incidents and adverse events can be tracked to a chain of errors that is influenced by technical and non-technical skills as well as environmental factors.

Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University GhentUpdated: Dec 22, 2025Locations: 1
Eligibility criteria

Patients undergoing elective (planned more than 48 hours) endovascular procedure... [+2]

No consent of patient [+3]

Status: Recruiting

Study on Prognosis of Acutely Ruptured Intracranial Aneurysms

The SPARTA study is a prospective multicenter observational trial in the Netherlands with the aim of identifying the best clinical care in patients with aneurysmal subarachnoidal haemorrhage. Differences in outcome between surgical treatment and endovascular treatment will be explored. Furthermore, cost effectiveness and radiological prognostic factors will be examined.

Participants needed: 880
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Haaglanden Medical CentreUpdated: Mar 25, 2025Locations: 6
Eligibility criteria

Confirmed diagnosis of subarachnoid haemorrhage on CT-scan or lumbar puncture (i... [+3]

Subarachnoid haemorrhage deemed most likely of 'perimesencephalic' origin after... [+4]

Status: Recruiting

Triage of Patients With Acute Ischemic Stroke Due to Large Vessel Occlusions-2

The objective of this study is to create a comprehensive, real-world, multi-center observational registry of consecutive patients admitted to hospitals with acute ischemic stroke (AIS) caused by large vessel occlusions (LVO), who are treated with either endovascular therapy (EVT) or the best available medical management (BMM).

Participants needed: 5,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Tianjin Huanhu HospitalUpdated: Dec 1, 2023Locations: 4Duration: 1 Year
Eligibility criteria

Patient admitted from Jan. 1st 2018 to Jan. 1st 2028; [+4]

Status: Not yet recruiting

Remote Ischemic Conditioning Combined With Endovascular Stenting for Symptomatic Intracranial Atherosclerotic Stenosis

The purpose of this registry is to evaluate the safety and efficacy of RIC for patients with symptomatic intracranial atherosclerotic stenosis (sICAS) undergoing endovascular therapy.

Participants needed: 160
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Tianjin Huanhu HospitalUpdated: Dec 16, 2022Locations: 1Duration: 12 Months
Eligibility criteria

Patient admitted from Jan. 1st 2023 to Jan. 1st 2025; [+4]

Stenosis of other causes; [+3]