Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Registry Study to Assess SYNTHECELTM Dura Repair

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.

Participants needed: 112
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: DePuy Synthes Products, Inc.Updated: Aug 11, 2026Locations: 4Duration: 24 Months
Eligibility criteria

Participant or legally authorized representative who is willing to participate i... [+1]

Status: Recruiting

A Study of VIRTUGUIDE System and DePuy Synthes Lapidus Implant in Participants Undergoing Lapidus Procedure

The purpose of this study is to assess the surgeon experience and surgery outcomes in participants undergoing index Lapidus procedure for the correction of hallux valgus (a foot deformity where the big toe angles outward towards the other toes, causing a painful bony bump at the base of the big toe joint) using the VIRTUGUIDE System and compatible DePuy Synthes Lapidus implants.

Participants needed: 100
Trial details
Age: 22+Biological sex: AllType: ObservationalSponsor: DePuy Synthes Products, Inc.Updated: Jul 31, 2026Locations: 8Duration: 12 Months
Eligibility criteria

Participants, both male and female, >= 22 years old at the time of consent [+4]

Participation in any other medical device or medicinal product study within the... [+4]

Status: Recruiting

FIBERGRAFT Aeridyan Posterolateral Fusion Study

This is a post-market, prospective, controlled, multicenter clinical study to evaluate radiographic fusion and clinical outcomes of FIBERGRAFT™ Aeridyan Matrix bone graft substitute in subjects who undergo a 1-3 level instrumented lumbar posterolateral fusion surgery. This clinical study will be conducted at up to 10 clinical sites within the United States.

Participants needed: 316
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: DePuy Synthes Products, Inc.Updated: Jul 6, 2026Locations: 8
Eligibility criteria

Subjects who require a 1-3 level instrumented PLF fusion in the lumbar spine in... [+2]

Subjects who had previous fusion surgery at the index level(s). [+17]