Actively Recruiting
Frailty, Quality Of Life and Early Reversal of Temporary Defunctioning Stoma in Ovarian Cancer
Led by Sahar Salehi · Updated on 2024-03-20
450
Participants Needed
4
Research Sites
263 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Complete macroscopic surgical resection (CMR) requires extensive surgery and combined with chemotherapy confers best chance of survival in advanced ovarian cancer. During cytoreductive surgery 11% of women require a temporary diverting intestinal stoma. Unexpectedly, our results from a unique fully accounted for population demonstrate that survival was not improved when increasing the proportion of women in whom CMR was achieved and in a yet unidentified subgroup of women extensive surgery was detrimental. In these women surgical treatment should be omitted in favor of chemotherapy only. Accordingly, there is an imperative need to improve patient selection to surgical treatment. In Sweden, we treat an unselected population of women in a public healthcare system, where 30% of women with are \>75 years. Despite these circumstances guidelines on patient-selection are lacking. Age is an imprecise variable to base clinical decisions on but must be considered with an aging population. The dynamics between physiological changes of aging, comorbidity and medical condition are included in the concept of frailty, that has gained little attention in oncology, despite their potential to stratify risk and mortality. The FOLERO study is a prospective adequately powered national cohort study with aim to determine if frailty instruments may be used to select patient to surgical treatment. In addition, we test the feasibility of early stoma reversal after index cytoreductive surgery in a small phase I trial and follow our patients Health Related Quality of Life after state of the art surgical treatment.
CONDITIONS
Official Title
Frailty, Quality Of Life and Early Reversal of Temporary Defunctioning Stoma in Ovarian Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women with epithelial ovarian cancer scheduled for cytoreductive surgery with curative intent
- Age 18 years
- Signed written informed consent
You will not qualify if you...
- Unable to understand Swedish or English
- Diagnosis other than ovarian cancer on final pathology
AI-Screening
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Trial Site Locations
Total: 4 locations
1
Karolinska University Hospital
Stockholm, Solna, Sweden, 171 76
Actively Recruiting
2
Sahlgrenska University Hospital and Sahlgrenska Academy
Gothenburg, Sweden, 41685
Not Yet Recruiting
3
Linköping University Hospital
Linköping, Sweden, 581 85
Actively Recruiting
4
Skåne University Hospital
Lund, Sweden, 22185
Not Yet Recruiting
Research Team
F
Fihima M Yusuf, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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