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NCT03373929: STITCH

Stitch Closure of PFO and Septal Repair

Status unknown NA Last updated 14 December 2017
What this trial tests

NA trial testing PFO Closure Rate in Foramen Ovale, Patent in 250 participants. Status unknown.

Timeline
20 November 2017
Primary endpoint
20 November 2019
20 November 2022

Quick facts

Lead sponsorHeartStitch.Com
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment250
Start date20 November 2017
Primary completion20 November 2019
Estimated completion20 November 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

HeartStitch.Com

Who can join

Adults 18 to 65, any sex, with Foramen Ovale, Patent or Septal Defect, Atrial. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the STITCH study is to evaluate closure rates of clinically relevant septal defects, including patent foramen ovale (PFO), Atrial Septal Defects (ASD - less than 1 cm with redundant septal tissue), trans septal puncture sites, repair of Atrial Septal Aneurysm (ASA) and rate of recurrent neurologic embolic events in patients with cryptogenic stroke and PFO.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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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/NCT03373929.

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