- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01661218
Complications and Risk Factors Related With Central Venous Catheters in Cancer Patients (CVCCP)
September 2, 2020 updated by: Beijing Huanxing Cancer Hospital
Complications and Risk Factors Related With Central Venous Catheters in Cancer Patients(CVCCP)
The investigators aim to determine the complications and risk factors related with peripherally inserted central catheters (PICCs) and central venous catheters (CVCs) in cancer patients.
Study Overview
Status
Completed
Conditions
Detailed Description
The purpose of this study is to determine the complications and risk factors related with peripherally inserted central catheters (PICCs) and central venous catheters (CVCs) in cancer patients.
Study Type
Observational
Enrollment (Actual)
3500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Beijing
-
Beijing, Beijing, China
- Beijing Huanxing Cancer Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All adult cancer patients with CVC and PICC placed at BeijingHCH and with written consent for this study
Description
Inclusion Criteria:
- all adult cancer patients with central venous catheters (CVCs) or peripherally inserted central catheters (PICCs) placed at BeijingHCH.
Exclusion Criteria:
- without written informed consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
complications
catheter-related venous thrombosis catheter-related infections
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Catheter-related venous thrombosis and catheter-related infections
Time Frame: 30 days after PICC and CVC line withdrawn
|
Catheter-related venous thrombosis and catheter-related infections
|
30 days after PICC and CVC line withdrawn
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Catheter tip position
Time Frame: participants will be followed before PICC and CVC line withdrawn
|
Catheter tip position
|
participants will be followed before PICC and CVC line withdrawn
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Jian DING, MD, Beijing Huanxing Cancer Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2012
Primary Completion (Actual)
August 1, 2019
Study Completion (Actual)
August 1, 2019
Study Registration Dates
First Submitted
August 2, 2012
First Submitted That Met QC Criteria
August 6, 2012
First Posted (Estimate)
August 9, 2012
Study Record Updates
Last Update Posted (Actual)
September 3, 2020
Last Update Submitted That Met QC Criteria
September 2, 2020
Last Verified
August 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HCH20120530
- HCH20120530-008 (Other Identifier: Beijing Huanxing Cancer Hospital)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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