Laparoscopic ventral hernia repair
ProcedurePatients operated with laparoscopic repair of ventral or incisional hernia
NCT Number: NCT01323361
The study aims to show variation in CA-125 and other inflammatory markers assumed to be a response to trauma and peritoneal inflammation in the perioperative period of laparoscopic ventral hernia repair
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Oslo University Hospital, Rikshospitalet, Oslo, Akershus, Norway
CA-125 and other inflammatory markers as body temperature, CRP, PCT, leucocytes and neutrophils measured pre- and post-operatively - correlated to trauma size i.e. area of dissection, mesh size, number of fixation points etc.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients operated with laparoscopic repair of ventral or incisional hernia
Time frame: 6 weeks post surgery
Oslo University Hospital
Other
Multi-centre Observational Pilot-study for Evaluation of Variation in CA-125 and Other Inflammatory Markers in the Perioperative Period of Laparoscopic Ventral Hernia Repair
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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.
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