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Post Approval Study to Evaluate the Safety and Performance of GENTA-FOIL Resorb® in Hand Surgery

NCT04482140 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2025-11-19

No results posted yet for this study

Summary

Single arm study to evaluate the safety and performance of Genta-Foil resorb® for the prevention of tissue adhesions

Conditions

  • Tissue Adhesions, Surgery-Induced

Interventions

DEVICE

Genta-Foil resorb®

Use of Genta-Foil resorb® to prevent adhesions in patients undergoing hand surgery

Sponsors & Collaborators

  • Newcastle-upon-Tyne Hospitals NHS Trust

    collaborator OTHER

  • KAT General Hospital

    collaborator OTHER

  • Advanced Medical Solutions Ltd.

    lead INDUSTRY

Principal Investigators

  • Stephen Lipscombe · Whiston Hospital Mersey and West Lancashire Teaching Hospitals NHS Trust, Warrington Rd, Rainhill, Prescot

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-14
Primary Completion
2025-11-07
Completion
2025-11-07

Countries

  • Greece
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04482140 on ClinicalTrials.gov