Køge Hospital
Køge, Region Sjælland, 4600, Denmark
NCT Number: NCT01484743
The Danish Ventral Hernia Database (DVHD) registers 37 different perioperative parameters. The aim of present study is to use large-scale data from DVHD to uncover risk factors for readmission, reoperation (any indication), death and reoperation for recurrence after parastomal hernia repair.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Køge, Region Sjælland, 4600, Denmark
All principal parastomal hernias registered in the Danish Ventral Hernia Database are included in the study. The included patients will be followed in up to 4 years in order to identify correlation between technical aspects of the hernia repair and postoperative morbidity.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
follow the risk for morbidity after incisional hernia repair
Time frame: up to 4 years after operation
Surgical risk factors for recurrence repair after parastomal hernia repair.
Zealand University Hospital
Other
Nationwide Prospective Study of Surgical Risk Factors for Poor Outcome After Parastomal Hernia Repair
Acronym: PAHEREP
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02121743
Parastomal Hernia, Terminal Colostomy
Amiens, France
View Trial DetailsNCT01380860
Hernia, Parastomal Hernia
Besançon, France
View Trial DetailsNCT07064694
Hernia, Parastomal Hernia
Warsaw, Poland
View Trial DetailsNCT06791642
Hernia, Parastomal Hernia
Naples, Italy
View Trial Details