UnknownNot Applicable

Preperitoneal Umbilical Mesh Area

Belgium20 participantsStarted 2023-02-01

Plain-language summary

The aim of this study is to measure the mesh shrinkage and the visualization of the mesh with MRI scan at 1 month and 13 months after robot assisted preperitoneal hernia repair using the visible CICAT mesh (Dynamesh®).

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Primary umbilical hernias up to 2 cm * Incisional hernias limited to zone M3 (EHS classification) and smaller than 2 cm Exclusion Criteria: * \<18 years * Emergency surgery (incarcerated hernia) * Clean-contaminated, contaminated or dirty procedures (according to the CDC classification) * Lateral hernias * Hernias close to the sternum or the pubic bone * Hernias bigger than 2 cm in diameter. * Hernias that need a component separation technique. * Previous mesh repair on the midline * ASA score\> 4 * Pregnancy * No patient Informed Consent * Life expectancy of less than 2years * Contraindications for MRI

What they're measuring

Change of mesh surface (percentage)

Timeframe: 1 month and 13 month post-operatively

Trial details

NCT IDNCT05576753

SponsorAlgemeen Ziekenhuis Maria Middelares

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-12-31

Contact for this trial

Maaike Vierstraete, MD

003292467400 maaikevierstraete@icloud.com

View on ClinicalTrials.gov More Ventral Hernia trials