Health Trials

Clinical trials

4

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

Condition / disease
Location
Status: Recruiting

Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry

The objective of this post market, clinical registry is to evaluate the performance of the products of the TVT family of products or vaginal vault or uterine prolapse repair (with laparotomic or laparoscopic approach including robotic assisted) using either Gynemesh PS Mesh or Artisyn Mesh in women undergoing surgery for SUI and POP.

Participants needed: 1,000
Trial details
Age: 21+Biological sex: FemaleType: ObservationalSponsor: Ethicon, Inc.Updated: Jun 26, 2026Locations: 10
Eligibility criteria

Stress urinary incontinence symptoms [+6]

Physical or psychological condition which would impair registry participation or... [+9]

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Status: Recruiting

A Study of ETHIZIA Versus SURGICEL Original in Controlling Soft Tissue Bleeding During Open Surgery

The objective of this clinical investigation is to evaluate the safety and efficacy of ETHIZIA to control minimal, mild, or moderate soft tissue bleeding during open surgery when compared to SURGICEL Original in the percentage of cases achieving hemostasis at 3 minutes after product application, and without re-bleeding up to 10 minutes after application.

Participants needed: 108
Trial details
Age: 22+Biological sex: AllType: InterventionalSponsor: Ethicon, Inc.Updated: Jun 5, 2026Locations: 7
Eligibility criteria

Participant is scheduled to undergo an elective open, abdominal, retroperitoneal... [+5]

Participant is scheduled for another planned surgery within the follow-up period... [+5]

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Status: Recruiting

GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study

The objective of this retrospective and prospective, single-arm, observational, multicenter, post-market study is to evaluate outcomes in women who underwent surgery for vaginal or uterine prolapse with a GYNEMESH PS Mesh.

Participants needed: 100
Trial details
Age: 21+Biological sex: FemaleType: ObservationalSponsor: Ethicon, Inc.Updated: Jun 5, 2026Locations: 3
Eligibility criteria

Female subjects who had laparotomic or laparoscopic abdominal sacrocolpopexy, in... [+3]

Subjects < 21 years of age at the time of informed consent [+2]

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Status: Recruiting

Post Market Clinical Follow-up Study on TVT ABBREVO® Continence System

The objective of this single arm, post market, clinical study is to evaluate the performance of Gynecare TVT ABBREVO® Continence System in women undergoing Mid-urethral sling surgery for Stress Urinary Incontinence (SUI).

Participants needed: 195
Trial details
Age: 21+Biological sex: FemaleType: ObservationalSponsor: Ethicon, Inc.Updated: Jun 5, 2026Locations: 4
Eligibility criteria

Stress urinary incontinence symptoms [+6]

Physical or psychological condition which would impair study participation or ar... [+7]

Read more