The Side of Implantable Central Vascular Catheters and Complications

Upper Extremity Deep Vein Thrombosis, Secondary Clinical Trial

Official title:

The Side of Implantable Central Vascular Catheters and Complications in Cancer Patients: A Randomization Observational Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01525277
• Other study ID #: 201110050RB
• Status: Recruiting
• Phase: N/A
• First received: January 31, 2012
• Last updated: April 11, 2014
• Start date: March 2012
• Est. completion date: December 2015

Study information

• Verified date: April 2014
• Source: National Taiwan University Hospital
• Contact: Yu-Yun Shao, MD
• Phone: 886223123456
• Email: yuyunshao[@]seed.net.tw
• Is FDA regulated: No
• Health authority: Taiwan: Department of Health
• Study type: Observational

Clinical Trial Summary

Whether the side of implantable CVCs was associated with the complication rates remains unclear. The investigators plan this study to explore this issue by randomizing patients to receive CVC implantation at the left subclavian or righ subclavian vein.

Description:

Implantable central venous catheters (CVC) are crucial for cancer patients. They provide central venous access for chemotherapy and high-concentration nutrition support. However, several potential CVC-related complications may develop and severely interfere with the patients' cancer treatment and can be life-threatening in some occasions.

Thrombotic events occurred in around 20% of cancer patients with implantable CVCs. Such events included intraluminal thrombosis and catheter-related venous thrombosis. Catheter removal was usually necessary to resolve these conditions. Treatment delays are inevitable for these patients. Besides, these thrombotic complications were associated with catheter-related infection, which could be highly dangerous for cancer patients.

Risk factors associated with these thrombotic events included the hypercoagulable state of the patients, the cancer types, the catheter types, and the placement of the catheter tips in the superior vena cava. Some single-arm studies found that CVC inserted from the left subclavian veins led to more CVC-related thrombosis than those inserted from the right subclavian vein. However, for most right-handed patients, to place these implantable CVCs on the right side is inconvenient for daily life because vigorous exercise was then impossible. Besides, these single-arm studies could not well control the other potentially interfering factors, such as the operators, catheter location and cancer types.

Therefore, we plan a randomized observational study to explore whether the side of implantable CVCs was actually associated with the complication rates. Cancer patients who need implantable CVCs will be randomized to have the catheters implanted either in the left subclavian vein or the right subclavian. Patients who had breast cancer, mediastinal mass with the diameter > 6 cm, ECOG performance score >2, or those who were not able to receive a standing P-A view chest X-ray will be excluded. Patients who had other reasons that prevented the randomization will also be excluded. The catheter-related complications will be actively reported by the patients. We will also enforce the records of complications by chart reviews and regular telephone contacts.

With the study, we can demonstrate whether a left-sided CVC and a right-sided CVC are different in complication rates. The result should be very useful in clinical practice.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 246
• Est. completion date: December 2015
• Est. primary completion date: June 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years and older

Eligibility

Inclusion Criteria:

1. Cancer patients who required implantable CVCs

2. Age > 20

3. Not previously implanted with implantable CVCs in subclavian veins.

Exclusion Criteria:

1. Breast cancer patients

2. Mediastinal mass > 6 cm

3. ECOG performance score > 2

4. Not able to receive a standing P-A view chest X-ray exam.

5. One of the subclavian veins has problems preventing randomization

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Upper Extremity Deep Vein Thrombosis
• Upper Extremity Deep Vein Thrombosis, Secondary
• Venous Thrombosis

Locations

Country	Name	City	State
Taiwan	National Taiwan University Hospital	Taipei City

Sponsors (1)

Lead Sponsor	Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	complication rates		everey 4 weeks	Yes