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NCT05812768: Suture-Tight™

Suture-Tight™ First-in-Human Safety and Performance Study

Status unknown NA Last updated 16 February 2024
What this trial tests

NA trial testing Suture-Tight Suture Delivery System in Aortic Aneurysm, Abdominal in 6 participants. Status unknown.

Timeline
12 December 2023
Primary endpoint
19 July 2024
31 July 2024

Quick facts

Lead sponsorVesteck, Inc.
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment6
Start date12 December 2023
Primary completion19 July 2024
Estimated completion31 July 2024
Sites1 location across Australia

Drugs / interventions tested

Conditions studied

Sponsor

Vesteck, Inc.

Who can join

21 and older, any sex, with Aortic Aneurysm, Abdominal. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Single center, open label, prospective, single-arm, first-in-human (FIH), pre-market clinical study with the objective of validating the safety and performance of the Suture-Tight™ Suture Delivery System in an EVAR procedure.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Aortic Aneurysm, Abdominal

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05812768.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing