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NCT03481140

Case Series Comparing Drains to TissuGlu® in a Donor Site DIEP Flap Breast Reconstruction Procedure

Completed Last updated 29 March 2018
What this trial tests

trial testing TissuGlu Surgical Adhesive in Deep Inferior Epigastric Perforator Flap Reconstruction in 58 participants. Completed in 30 November 2017.

Timeline
21 April 2015
Primary endpoint
30 November 2017
30 November 2017

Quick facts

Lead sponsorCohera Medical, Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment58
Start date21 April 2015
Primary completion30 November 2017
Estimated completion30 November 2017

Drugs / interventions tested

Conditions studied

Sponsor

Cohera Medical, Inc.

Who can join

18 and older, any sex, with Deep Inferior Epigastric Perforator Flap Reconstruction. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To evaluate the safety and effectiveness of a lysine-derived urethane adhesive (TissuGlu® Surgical Adhesive) as a less invasive alternative to surgical drains in the abdominal donor site for deep inferior epigastric perforator (DIEP) flap reconstruction.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Three-Dimensional Disassemblable Scaffolds for Breast Reconstruction.
    Kiseleva V, Bagdasarian A, Vishnyakova P, Elchaninov A, et al · · 2025 · PMID 40808084 · DOI 10.3390/polym17152036

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Other trials of TissuGlu Surgical Adhesive

Trials testing the same drug.

Other Cohera Medical, Inc. trials

Trials by the same sponsor.

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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/NCT03481140.

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