Post Market Study of Tutopatch In Craniotomy

NCT07118020 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 75

Last updated 2025-11-25

No results posted yet for this study

Summary

This is a post market prospective, multi-center study of up to 75 participants at approximately 8 clinical study sites. The objective of the study is to evaluate safety by assessing incidence of device and/or procedure related adverse events.

Conditions

  • Craniotomy

Sponsors & Collaborators

  • RTI Surgical

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-09-21
Primary Completion
2027-12-31
Completion
2027-12-31

Countries

  • Austria
  • Spain

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 NCT07118020 on ClinicalTrials.gov