Assessment of Complications, Quality of Life and Easiness of Use of Implantable Central Venous Access Ports (CCI)

Centre Oscar Lambret

Status: Completed

Conditions: Cancer

Study type: Observational

Funder types: Other

Identifiers

NCT00921141

CCI

Details and patient eligibility

About

This is a prospective, descriptive and observational study of the anticancer center practice

Enrollment: 815 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient with any cancer, requiring a central venous catheter
• No contraindication for any surgery with local or complete anaesthesia

Exclusion criteria

• Previous Xylocaine or Lidocaine allergy
• Clinic superior vena cava syndrome

Trial design

815 participants in 1 patient group

study population

Description:

Patient with cancer requiring a long-term central venous catheter