Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT03268876

The INFLUENCE of Cytoreduction on PRO in EOC

The INFLUENCE of Cytoreduction on Patient Reported Outcomes in Patients With Epithelial Ovarian Cancer

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
70 (estimated)
Sponsor
Haukeland University Hospital · Academic / Other
Sex
Female
Age
18 Years – 100 Years
Healthy volunteers

Summary

Based on an improved understanding of how the extent of successful cytoreduction is influenced both by inherent tumor biological characteristics as well as the aggressiveness of the surgical approach this project aims to better define the value of cytoreduction and to use the knowledge gained to develop more individualized therapy and follow-up. This will be achieved through a translational biomedical research approach. Due to the research group's traditions clinical phenotyping, biomarker identification, and clinical trials will be the focus.

Detailed description

The patients will be recruited at their follow-up appointment after their surgery. At this consultation the patient will be informed about the final diagnosis and extent of disease and a plan for their further chemotherapeutic treatment will be developed. All patients will be offered carboplatin AUC 5 and paclitaxel 175mg/m2 q3w for 6 cycles \[+ bevacizumab 7.5mg/kg q3w for 18 cycles in high-risk women of recurrence (IIIc not maximal debulked with a rest tumor of \>1 cm2 and stage IV)\]. In they fulfill the inclusion criteria and agree the inform consent formula will be signed. During the screening period the study team will secure that the necessary information needed is available and study specific test and analysis will be undertaken. After inclusion the study specific consultations will be scheduled coinciding with the patient regular appointments for treatment and follow-up. The patients will be followed at predetermined time points (after finalizing the chemotherapy; and every 3 months thereafter for 2 years).

Conditions

Timeline

Start date
2021-03-03
Primary completion
2025-12-28
Completion
2030-12-31
First posted
2017-08-31
Last updated
2024-10-09

Locations

3 sites across 1 country: Norway

Source: ClinicalTrials.gov record NCT03268876. Inclusion in this directory is not an endorsement.