Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:51 AM
Ignite Modification Date:
2025-12-25 @ 2:51 AM
NCT ID:
NCT03680833
Eligibility Criteria:
Inclusion Criteria:
* Women of age 18 years and older at the time of informed consent.
* Women with a pathologically proven cervical carcinoma of any histologic subtype, clinically stage 1a2- 2a1 planned for primary surgery
* Absence of any exclusion criteria
Exclusion Criteria:
* Non consenting patients
* Ongoing pregnancy
* Inability to understand written and/or oral study information
* Who performance status III or more
* Previous lower limb lymphedema
* Surgical contraindication to a laparoscopic approach or lymphadenectomy at surgeons discretion.
* Anesthesiologic contraindication to a laparoscopic approach at the anesthetist's discretion
* Locally advanced disease or intraabdominal/distant metastases at preoperative CT, MRI or ultrasonography
* Radiologically suspect pelvic nodal metastatic disease according to the RECIST criteria (\>= 1 node with \>=16 mm short axis diameter)
* Allergy to Iodine
* Patients with a known liver disease
* Patients with a significant bleeding disorder or mandatory antithrombotic treatment.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT03680833
Study Brief:
Protocol Section:
NCT03680833