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Clinical Trials/NCT04083547
NCT04083547CompletedNot Applicable

Cirkulerande Tumörceller Hos Patienter Med Bukhinnespridda tumörer

Uppsala University1 site in 1 country114 target enrollmentStarted: October 17, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
114
Locations
1
Primary Endpoint
Prognostic value

Study Overview

Brief Summary

This study aims to evaluate the prognostic value of circulating tumour cells (CTC) in patients undergoing cytoreductive surgery and hyperthermic intraperitoneal chemotherapy due to gastrointestinal cancers that have spread to the peritoneum.

Detailed Description

CTCs har extracted by way of a new method at baseline, during surgery, and postoperatively. The occurence of such CTCs will be investigated for prognostic evaluation. Patients will be follow-up by Clinical routine. Disease recurrence and overall survival will be the endpoint used.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Peritoneal metastases being treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Prognostic value

Time Frame: 2 year.

Prediction of survival and recurrence according to the occurrence of CTCs.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Uppsala University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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