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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04083547
Other study ID # CTC study
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 17, 2017
Est. completion date November 1, 2020

Study information

Verified date November 2020
Source Uppsala University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 114
Est. completion date November 1, 2020
Est. primary completion date October 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Peritoneal metastases being treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
iCellate
New method of circulating tumour cell detection and capture.

Locations

Country Name City State
Sweden Akademiska Sjukhuset (Uppsala University hospital) Uppsala

Sponsors (1)

Lead Sponsor Collaborator
Uppsala University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prognostic value Prediction of survival and recurrence according to the occurrence of CTCs. 2 year.
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