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Clinical Trials/NCT01628328
NCT01628328CompletedNot Applicable

Impact of Metallic Stent Insertion for Obstructing Colorectal Cancer on Circulating Tumor Cell Dissemination

The University of Hong Kong0 sites40 target enrollmentStarted: July 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Primary Endpoint
Changes of circulating tumor cell level before and after colonic stenting for patients with obstructive colorectal cancer

Study Overview

Brief Summary

This study aims to examine the hypothesis of tumor cell dissemination after colonic stenting for obstructing colorectal cancer by measuring the level of plasma circulating tumor cell before and after the procedure of successful colonic stenting in patients.

Detailed Description

  1. Patient recruitment:

Patients will be recruited from the Division of Colorectal Surgery, Department of Surgery, the University of Hong Kong, over a 12 - 18 months period. Our institution is a tertiary referral center for colorectal cancer patients in Hong Kong. Informed consent will be obtained from the patients after the inclusion criteria are met.

The study plans to recruit 25 patients in the colonic stenting group to compare with 15 patients in the control group.

Inclusion criteria:

Colonic stenting group

  1. Patients with obstructive colorectal cancer that requires colonic stenting as treatment
  2. Age > 18 years and is able to give informed consent
  3. Informed consent for blood collection obtained

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

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

Inclusion Criteria

  • Colonic stenting group
  • Patients with obstructive colorectal cancer that requires colonic stenting as treatment
  • Age > 18 years and is able to give informed consent
  • Informed consent for blood collection obtained
  • Control group
  • Patients with colorectal cancer who have colonoscopy without stenting
  • Age > 18 years and is able to give informed consent
  • Informed consent for blood collection obtained

Exclusion Criteria

  • Patients who refuse or who is unable to give informed consent on blood taking for the study.

Outcomes

Primary Outcomes

Changes of circulating tumor cell level before and after colonic stenting for patients with obstructive colorectal cancer

Time Frame: Before and first 3 days after procedure

The patients' peripheral blood will be collected before and on first 3 days after the procedure.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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