Prospective Study of Minimally Invasive (Laparoscopic and Robotic) Hernia Repair (Incisional and Primary, Midline and Lateral, Not Inguinal)
Recruiting
Observational Study
Ventral Hernia Midline
Hernia Lumbar
Incisional Hernia Repair
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 400 (estimated)
- Sponsor
- Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz · Other
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About This Trial
The participating researchers register all adult patients (who have given informed written consent) scheduled for elective repair of an abdominal wall hernia (NOT inguinal hernias) via minimally invasive operation technique (i.e.: laparoscopy or robotic repair) and perform a follow up of 5 years to analyze clinical outcome parameters. These parameters include recurrence of the hernia, intra- and p…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Indication for elective minimally invasive ventral hernia repair due to criteria of the participating surgeons
Exclusion Criteria:
* Patient rejects participation or giving written informed consent
* Positive pregnancy test (Beta HCG in serum)
* Patients who do not meet crit…
Contacts