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NCT01993888 · ClinicalTrials.gov registry record · Phase 3

The EVARREST® Fibrin Sealant Patch Liver Study

A Phase 3 study, sponsored by Ethicon.

Completed
Registry status
Phase 3
Development phase
102
Enrollment target

NCT01993888: Completed Phase 3 study, sponsored by Ethicon.

NCT01993888 is a Phase 3 study that has completed, run by Ethicon. The registered enrollment target is 102 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01993888, a Phase 3 study, has completed, sponsored by Ethicon.

COMPLETED
Registry status
Phase 3
Development phase
102 participants
Enrollment target

Study Summary

To evaluate the safety and hemostatic effectiveness of EVARREST® Fibrin Sealant Patch (EVARREST) versus standard of care treatment (SoC) in controlling parenchymal bleeding during hepatic surgery.

Primary Outcome

Proportion of subjects achieving hemostasis at the TBS at 4-minutes following randomization and with no re-bleeding requiring treatment at the TBS any time prior to initiation of wound closure. Hemostasis is defined as no detectable bleeding at the TBS.

Interventions

  • BIOLOGICAL EVARREST® Fibrin Sealant Patch
  • OTHER Standard of Care (SoC)

Trial Details

FieldValue
Enrollment Target 102 participants
Start Date 2013-10
Est. Completion 2014-09
Phase Phase 3
Ethicon

38 total trials

What the finished NCT01993888 record still lists

NCT01993888 is an interventional study that assigns participants to a tested intervention. The registered 102 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (87% lower).

The record links to 0 conditions, and to 2 interventions - of which EVARREST® Fibrin Sealant Patch is the first listed.

NCT01993888 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01993888 about?

NCT01993888 is a clinical study titled "The EVARREST® Fibrin Sealant Patch Liver Study". To evaluate the safety and hemostatic effectiveness of EVARREST® Fibrin Sealant Patch (EVARREST) versus standard of care treatment (SoC) in controlling parenchymal bleeding during hepatic surgery.

What is the current status of trial NCT01993888?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 102 participants. The study started on 2013-10. Estimated completion is 2014-09.

What interventions are being tested in trial NCT01993888?

The interventions under investigation include: EVARREST® Fibrin Sealant Patch (BIOLOGICAL), Standard of Care (SoC) (OTHER).

Who is sponsoring clinical trial NCT01993888?

This trial is sponsored by Ethicon, which has 38 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01993888's enrollment target sits among peer trials

102 1676th of 2000 higher than 321 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT01993888, the US trial registry maintained by the National Library of Medicine. NCT01993888 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.