Autopsy report · NCT03912662

ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention

“Surgical complications arose early in the study, mainly due to patient complexity, not to study device or implantation. Despite refining protocol to exclude highly complex patients, these issues persisted, leading to the study's early termination.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 6 months before it started.
• Ran for about 3 years before it stopped.
• 32 participants enrolled.
• Results were posted on the registry 3 years 3 months after it ended.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

Medtronic - MITG

Sponsor type

Industry

Conditions

Incisional Hernia

Interventions

Mesh augmented reinforcement

Participants

32

Sites

11

Countries

France

Look deeper

• The official registry record (the source of truth)
• Record history: every change the sponsor made
• Open it in the database

Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.