Duygu
Istanbul, Turkey (Türkiye)
NCT Number: NCT06648330
This study was designed as a prospective observational study.
Looking for future studies?
Notify Me18 year and older
Female
Observational
Istanbul, Turkey (Türkiye)
In this study, the investigator planned to evaluate the effect of blood lactate levels on postoperative gastrointestinal morbidity after paraaortic retroperitoneal lymph node dissection. In gynaecological surgeries, following the removal of the intestines from the surgical field, the retroperitoneal space is entered and the main vessels such as the vena cava inferior and aorta are accessed through the left or right approach depending on the experience and habit of the per-operative surgeon, and total systemic lymph node dissection or bulky lymph node excision is performed depending on the case. During the removal of the intestines from the surgical field, hypoperfusion may develop due to decreased blood flow to the intestines. for this purpose, the investigator planned to investigate the relationship between the change in blood gas lactate values and postoperative gastrointestinal complications in this process.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The relationship between lactate level and mesenteric ischaemia in gynaecological cancer surgeries with paraaortic retroperitoneal lymph node dissection will be evaluated.
Time frame: intraoperatively
Change from baseline in lactate levels in paraaortic lymph node dissection
Duygu Akyol
Other Gov
The Effect of Blood Lactate Levels on Postoperative Gastrointestinal Morbidity After Paraaortic Retroperitoneal Lymph Node Dissection
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.
NCT04445428
COVID, Morbidity
Bissau, Guinea-Bissau
View Trial DetailsNCT04065828
Morbidity, Oral Health
View Trial DetailsNCT03885206
Co-morbidity, Medical Emergencies
Sarpsborg, Østfold fylke, Norway
View Trial DetailsNCT03460002
Children, Measles Vaccination
Bissau, Guinea-Bissau
View Trial Details