Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Instituto de Investigacion Sanitaria La Fe
The objective of this study is to describe the feasibility of performing the sentinel node technique (Detection rate) in patients with early stage ovarian cancer.
With this research study it will be evaluated the concordance of the result between two diagnostic tests: Sentinel node and Pelvic-para-aortic lymphadenectomy in patients with ovarian cancer.
Age
18–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
Informed consent signed previously to performing any procedure related to the clinical trial.
Patients who are women 18 years of age or older at the moment of the randomization.
Patients with anatomopathological diagnosis of malignant ovarian tumor in a deferred study proposals for staging surgery or patients with suspicious tumor of malignancy who are going to be subjected to exploratory lapaotomy or laparoscopy and operative biopsy, and in the case this is positive, surgery of staging will be performed .
You may not be if
Informed consent not obtained or withdraw.
Benign result in extemporaneous study
Previous history of vascular surgery in the aorta, cava or pelvic vessels
Previous pelvic or para-aortic lymphadenectomy
Previous lymphoma
Previous abdomino-pelvic tumor
Previous allergic reaction to indocyanine green
Pregnancy / lactation
Severe adherent syndrome
Clareo Health | Sentinel Lymph Node in Early Ovarian Cancer
