# The Use of CoSeal (Sealant Agent) in Patients During Left Ventricular Assist Device Surgery

> **NCT01605019** · NA · TERMINATED · sponsor: **The Methodist Hospital Research Institute** · enrollment: 4 (actual)

## Conditions studied

- Heart Failure
- Ventricular Dysfunction

## Interventions

- **DEVICE:** CoSeal
- **DEVICE:** BioGlue® Surgical Adhesive

## Key facts

- **NCT ID:** NCT01605019
- **Lead sponsor:** The Methodist Hospital Research Institute
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2012-06
- **Primary completion:** 2014-03
- **Final completion:** 2014-03
- **Target enrollment:** 4 (ACTUAL)
- **Why stopped:** funding for study stopped
- **Last updated:** 2018-08-31


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01605019

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01605019, "The Use of CoSeal (Sealant Agent) in Patients During Left Ventricular Assist Device Surgery". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT01605019. Licensed CC0.

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