A Registry Study to Assess SYNTHECELTM Dura Repair

Part of paid clinical trials in Weston, Florida.

Sponsor
DePuy Synthes Products, Inc.
Study ID
NCT07758790
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

  • Craniotomy

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Study Details

The purpose of this study is to assess how safe synthecel dura repair is and how well it performs in participants undergoing cranial surgery requiring dura repair (a procedure to close and protect the outer covering of the brain) in a regular, everyday healthcare environment.

Key Dates

First listed
Aug 11, 2026
Start date
Jul 31, 2026
Status verified
Aug 2026
Primary completion
Oct 31, 2029
Completion
Mar 31, 2030

Study Design

Enrollment
112 participants (estimated)

Arms

  • Arm: SYNTHECEL Dura Repair
    Participants undergoing cranial dura repair will be enrolled to monitor the safety and performance of SYNTHECEL dura repair.

Primary Outcome Measure

Demographics Characteristic Of Participants: Age [ Time Frame: At baseline ]

Central Contacts

Locations (4)

FacilityCityStateZIPSite coordinators
Cleveland ClinicWestonFlorida33331 3609-
University of KentuckyLexingtonKentucky40536-
Kettering Medical CenterKetteringOhio45429-
Baylor College of MedicineHoustonTexas77030-

Find similar trials in Weston, FL

By research site
Cleveland Clinic· Weston, FLUniversity of Kentucky· Lexington, KYKettering Medical Center· Kettering, OHBaylor College of Medicine· Houston, TX