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:
2025-12-26 @ 5:24 PM
Ignite Modification Date:
2025-12-26 @ 5:24 PM
NCT ID:
NCT00844506
Eligibility Criteria:
Inclusion Criteria:
* Written informed consent.
* Histological proven epithelial ovarian carcinoma.
* At least 4 weeks after termination of the last course of chemotherapy.
* Rising CA-125 serum levels after "first line" treatment and no measurable disease according to the RECIST (Response Evaluation Criteria in Solid Tumours) criteria, or Rising CA-125 serum levels after "first line" treatment with measurable disease according to the RECIST (Response Evaluation Criteria in Solid Tumours) criteria, but not willing or otherwise not fit to receive "second line" chemotherapy.
* Age 18 years or older, and an life expectancy of at least 3 months.
* Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial.
* Performance status 0 to 2 (WHO scale).
* Adequate hepatic, renal, and bone marrow function as defined:
ASAT \< 100 U/l; ALAT \< 113 U/l; PT 9-12 seconds; APTT 23-33 seconds; creatinine \< 135 μmol/l; WBC \> 3.0 x 109/L; platelets \> 100 x 109/L; hemoglobin \> 6.0 mmol/l.
\- Adequate venous access for blood collection and i.v. administration of cyclophosphamide.
Exclusion Criteria:
* Pregnancy and / or breast feeding.
* (A)symptomatic cystitis.
* Other malignancies (previous or current), except basal or squamous cell carcinoma of the skin.
* Immunosuppressive agents, except for topical and inhalation corticosteroids.
* Prior therapy with a biological response modifier.
* Any other major disease that may interfere with the conduct of the study (e.g. uncontrolled hypertension, severe and/or unstable heart disease, neurological and psychiatric disorders).
* Signs or symptoms of CNS metastases.
* Known substance abuse (drug or alcohol).
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT00844506
Study Brief:
Protocol Section:
NCT00844506