Know Cancer

or
forgot password

Assessment of Complications, Quality of Life and Easiness of Use of Implantable Central Venous Access Ports : Cohort and Prospective Study


N/A
18 Years
N/A
Not Enrolling
Both
Cancer

Thank you

Trial Information

Assessment of Complications, Quality of Life and Easiness of Use of Implantable Central Venous Access Ports : Cohort and Prospective Study


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

Type of Study:

Observational

Study Design:

Observational Model: Case-Only, Time Perspective: Prospective

Outcome Measure:

Incidence and collection of complications for the patients requiring an implantable central venous access ports substitution/change

Outcome Time Frame:

Until the implantable central venous access ports removal

Safety Issue:

No

Principal Investigator

Fabrice NARDUCCI, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Centre Oscar Lambret

Authority:

France: National Consultative Ethics Committee for Health and Life Sciences

Study ID:

CCI

NCT ID:

NCT00921141

Start Date:

May 2006

Completion Date:

April 2009

Related Keywords:

  • Cancer
  • Implantable central venous access ports, cancer

Name

Location