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 @ 4:07 AM
Ignite Modification Date:
2025-12-25 @ 4:07 AM
NCT ID:
NCT06820320
Eligibility Criteria:
Inclusion Criteria:
* Patients between the ages of 18 and 75 years;
* Patients underwent retroperitoneal or extended lymphadenectomy for abdominal or pelvic malignant tumors;
* Patients diagnosisted with postoperative Chylous ascites. Chylous ascites were defined by the presence of non-infectious, milky, or creamy effluent in drainage tubes surpassing 200 mL daily, paired with triglyceride concentrations exceeding 110 mg/dL
Exclusion Criteria:
* Patients with severe cardiac, hepatic and renal insufficiency;
* Patients with a history of iohexol allergy or allergy to contrast media;
* Patients who have received other interventions;
* Patients with severe intestinal obstruction or intestinal perforation;
* Patients who are unable to comply with the requirements of the study or are unable to complete follow-up.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06820320
Study Brief:
Protocol Section:
NCT06820320