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:
2025-12-24 @ 11:32 PM
Ignite Modification Date:
2025-12-24 @ 11:32 PM
NCT ID:
NCT02217956
Eligibility Criteria:
Inclusion Criteria:
1. Stage IIIC unresectable ovarian, tubes or peritoneal primitive adenocarcinoma according to FIGO classification previously treated with 6 cycles of carboplatin-cisplatin neoadjuvant chemotherapy with a response allowing complete surgery after the 6 cycles
2. Time frame between the sixth platin injection and the CRS + HCIP \< 10 weeks
3. No disease progression during the neoadjuvant chemotherapy
4. 18 \</= âge \</= 65 ans
5. Performance Status OMS \< 2
6. Hematological function : PNN \>/= 1.5x10\^9/L, platelets \>/= 150x10\^9/L, hemoglobin \> 9 g /dl (transfusion allowed)
7. Hepatic function : Bilirubin \</= 1,5 x LSN, ASAT (SGOT) and ALAT (SGPT) \</= 3 x LSN, Phosphatases alkaline \</= 3 x LSN
8. No kidney related pathology, plasmatic creatinine \< 140 µmol/l, creatinine clearance \> 60 ml/min (Cockcroft formula) and urinary strip \<2 (If urinary strip \>/= 2, proteinuria \< 1g/24h)
9. Plasmatic albumine \> 25 g/l
10. HIV negative status
11. Affiliation to social security
12. Signed informed consent
Exclusion Criteria:
1. Incomplete cell kill surgery
2. Non-epithelial ovarian cancer
3. Borderline tumors
4. Non in complete remission previous cancer for more than 5 five years before inclusion
5. Uncontrolled high blood pressure (blood pressure \> 150/100 mm Hg despite antihypertensive treatment)
6. Previous abdominal or pelvic radiotherapy
7. Previous pathology of the central nervous system, except for well controlled pathology like epilepsy
8. Previous stroke, transient ischemic attacks or subarachnoid hemorrhage
9. Previous pulmonary embolism
10. Pregnant or breastfeeding women (Women in age must have a blood negative pregnancy test at least 15 days before going under surgery)
11. Participation to an other clinical trial within 30 days before inclusion in the study
12. Known hypersensitivity to platin or bevacizumab
13. Not healed wound, ulcer or bone fracture
14. Previous haemorrhagic or thrombotic malfunction \< 6 months
15. Significant CArdiovascular disorder including:
* Heart attack or unstable angina within the 6 months before inclusion
* Grade \> 1 congestive heart failure according to the NYHA classification
* Uncontrolled cardiac arrhythmia despite of treatment (patients with atrial fibrillation for which the pace is under control can be include)
16. Long term or recent (within 10 days before inclusion) medication using Aspirin at dosage \> 325 mg/day
17. Long term or recent (within 10 days before inclusion) medication using anticoagulant per os or parenteral or thrombolytic given at full dosage for therapeutic purpose.
18. Grade \> 1 previous sensory and motor neuropathies according to CTC AE V4.0
19. Previous abdominal fistula, GI perforation or intra-abdominal abscess within 6 months before first administration of bevacizumab
20. Proof of any other disease, metabolic malfunction, physical or laboratory exam showing any possibility of disease or condition contraindicating administration of the drug under trial or exsposing the patient to several complications related to the treatment.
21. Persons deprived of liberty
22. Impossibility to comply with the medical following of the treatment for geographical, social or mental reason
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT02217956
Study Brief:
Protocol Section:
NCT02217956