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RECRUITING Phase 3

A Study to Compare the Efficacy and Safety of TachoSil and Surgicel Original as an Adjunct to Control Mild to Moderate Soft Tissue Bleeding During Surgery

NCT06664775 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this clinical study is to assess the efficacy and safety of TachoSil compared to the widely known and used for \> 60 years local hemostatic product Surgicel Original as an adjunct to control mild to moderate soft tissue bleeding during surgery.

Conditions Studied

Interventions

  • BIOLOGICAL TachoSil
  • BIOLOGICAL Surgicel Original

Study Locations (9)

California

  • Torrance Memorial — Torrance

Colorado

  • St. Anthony Hospital — Lakewood

District of Columbia

  • Georgetown University — Washington D.C.

Illinois

  • University Of Chicago — Chicago

Indiana

  • Indiana University — Indianapolis

Kentucky

  • University of Louisville — Louisville

Missouri

  • Washington University — St Louis

North Carolina

  • Atrium Health Carolinas Medical Center — Charlotte

Trial Details

FieldValue
Enrollment Target 116 participants
Start Date 2025-04-02
Est. Completion 2026-06-30
Phase Phase 3

Sponsor

Corza Medical

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06664775

The ClinicalTrials.gov registry entry for NCT06664775 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 116 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Corza Medical, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Hemorrhage appearing as the primary indexed condition, and to 2 interventions — of which TachoSil is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06664775 reports 9 study locations spanning 9 distinct geographic areas — top geographies include California, Colorado, District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06664775 about?

NCT06664775 is a clinical study titled "A Study to Compare the Efficacy and Safety of TachoSil and Surgicel Original as an Adjunct to Control Mild to Moderate Soft Tissue Bleeding During Surgery". The purpose of this clinical study is to assess the efficacy and safety of TachoSil compared to the widely known and used for \> 60 years local hemostatic product Surgicel Original as an adjunct to control mild to moderate soft tissue bleeding during surgery.

What is the current status of trial NCT06664775?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 116 participants. The study started on 2025-04-02. Estimated completion is 2026-06-30.

What conditions does trial NCT06664775 study?

This clinical trial studies the following conditions: Hemorrhage. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06664775?

The interventions under investigation include: TachoSil (BIOLOGICAL), Surgicel Original (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06664775?

This trial is sponsored by Corza Medical, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06664775 being conducted?

This trial has 9 study locations across California, Colorado, District of Columbia, Illinois, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial