Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06298877

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

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women with epithelial ovarian cancer scheduled for cytoreductive surgery with curative intent
  • Age 18 years
  • Signed written informed consent
Not Eligible

You will not qualify if you...

  • Unable to understand Swedish or English
  • Diagnosis other than ovarian cancer on final pathology

AI-Screening

AI-Powered 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

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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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