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NCT00674128 · ClinicalTrials.gov registry record · NA

Comparison of Cyanoacrylate Tissue Adhesive and Suture for Closure of Cardiac Device Pockets

A NA study, sponsored by Mayo Clinic.

Terminated
Registry status
NA
Development phase
103
Enrollment target

NCT00674128: Clinical Trial NA study, sponsored by Mayo Clinic.

NCT00674128 is a NA study that was terminated before completion, run by Mayo Clinic. The registered enrollment target is 103 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00674128, a NA study, was terminated before completion, sponsored by Mayo Clinic.

TERMINATED
Registry status
NA
Development phase
103 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether cyanoacrylate tissue adhesive is as effective as polyglactin 910 suture for surgical closure of cardiac device pockets.

Interventions

  • DEVICE Cyanoacrylate tissue adhesive (Dermabond)
  • DEVICE Polyglactin 910 suture (Vicryl)

Trial Details

FieldValue
Enrollment Target 103 participants
Start Date 2008-05
Est. Completion 2009-05
Phase NA
Mayo Clinic

2,844 total trials

Why NCT00674128 stopped before completion

NCT00674128 is an interventional study that assigns participants to a tested intervention. The registered 103 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 2 interventions - of which Cyanoacrylate tissue adhesive (Dermabond) is the first listed.

NCT00674128 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00674128 about?

NCT00674128 is a clinical study titled "Comparison of Cyanoacrylate Tissue Adhesive and Suture for Closure of Cardiac Device Pockets". The purpose of this study is to determine whether cyanoacrylate tissue adhesive is as effective as polyglactin 910 suture for surgical closure of cardiac device pockets.

What is the current status of trial NCT00674128?

This trial is currently terminated. It is a NA study. The enrollment target is 103 participants. The study started on 2008-05. Estimated completion is 2009-05.

What interventions are being tested in trial NCT00674128?

The interventions under investigation include: Cyanoacrylate tissue adhesive (Dermabond) (DEVICE), Polyglactin 910 suture (Vicryl) (DEVICE).

Who is sponsoring clinical trial NCT00674128?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00674128's enrollment target sits among peer trials

103 837th of 2000 higher than 1,164 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00674128, the US trial registry maintained by the National Library of Medicine. NCT00674128 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.