activating the Immune response In ovarian cancer study
- Conditions
- ovarian carcinomamalignant ovarian tumors10027656
- Registration Number
- NL-OMON56684
- Lead Sponsor
- Catharina-ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 90
-Subjects should be at least 18 years old and mentally competent
-Newly diagnosed patients with ovarian carcinoma (OC) who go for primary
debulking surgery or patients with OC are scheduled for interval debulking
- Controls: women who undergo surgery for benign gynaecological conditions
under general anaesthesia
-Mentally incompetent
-Pregnant or breastfeeding
-Known inflammatory or infectious diseases or an immunosuppressive status
-Using medication interfering with the immune system
-Severe comorbidities: other active malignancy (except for basal cell carcinoma
and other in situ carcinomas)
-Serious psychiatric pathology
-A self-reported alcohol consumption of >21 units per week
-Bleedings disorder
-History of splenectomy
-Not mastering the Dutch language
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Characterizing the immune status of ovarian carcinoma patients compared to<br /><br>cancer-free controls, with a focus on hematopoietic organs and the immune cells<br /><br>originating from them. This will be accomplished by assessing the<br /><br>transcriptional, epigenetic, and functional programming of circulating<br /><br>monocytes and myeloid precursor cells in OC.</p><br>
- Secondary Outcome Measures
Name Time Method <p>none</p><br>