CA125 Levels and Other Inflammatory Markers in Laparoscopic Ventral Hernia Repair
NCT ID: NCT01323361
Last Updated: 2013-01-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
10 participants
INTERVENTIONAL
2011-04-30
2012-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Natural Orifice Translumenal Endoscopic Surgery (NOTES): Laparoscopic Assisted Transvaginal Ventral Hernia Repair
NCT01398215
Risk Factors and Complications of Ventral Hernia Repair
NCT02292264
Prolonged Hospital Stay and Readmission After Elective Ventral Hernia Repair
NCT01388634
Reoperation Rate Versus Clinical Recurrence After Ventral Hernia Repair
NCT01325246
Risk Factors of Incisional Hernias After Emergency Midline Laparotomy
NCT05509452
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Non-immunosupressed
Normal population
Laparoscopic ventral hernia repair
Patients operated with laparoscopic repair of ventral or incisional hernia
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Laparoscopic ventral hernia repair
Patients operated with laparoscopic repair of ventral or incisional hernia
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* ASA above III
* Liver failure
* Abnormal CA-125 prior to surgery
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sykehuset Innlandet HF
OTHER
Oslo University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Jan Lambrecht
MD
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
jan r lambrecht, md
Role: STUDY_DIRECTOR
Sykehuset Innlandet HF
ole m øyen, Dr. Med.
Role: STUDY_CHAIR
Oslo University Hospital
erik trondsen, Dr. Med.
Role: STUDY_CHAIR
Oslo University Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Oslo University Hospital, Rikshospitalet
Oslo, Akershus, Norway
Sykehuset Innlandet HF
Gjøvik, Oppland, Norway
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2010/29472
Identifier Type: OTHER
Identifier Source: secondary_id
2010/3264-1 (REK)
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.