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N/A
18 Years
N/A
Open (Enrolling)
Both
Chromaffin-tissue Derived Tumors

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Trial Information


Inclusion Criteria:



- Age + 18 years. The women in ages to procreate have to have an effective
contraception or a negative pregnancy test (in the absence of effective
contraception) Having a radiological and functional imaging (balance
sheet(assessment) pré--IBZM) considered adapted and complete for the pathology.

- Having a phéochromocytome or a paragangliome proving a surgical operation in view of
the data of the balance sheet(assessment) pré--IBZM.

- With or without allergy in the iodine.

Exclusion Criteria:

- NEM2A or 2B.

- Malignant Forms which do not recover from an even partial, surgical
gesture(movement).

- Pregnant Women or in the course of feeding.

- Women in age to procreate without effective contraception, with positive pregnancy
test.

- Renal insufficiency

Type of Study:

Interventional

Study Design:

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

The aim of the present study is to evaluate the feasibility of 123I-IBZM (a D2 agonist radiolabelled with 123I) in patients with PHEO and/or PGL. Diagnostic accuracy will be also compared to traditional SPECT imaging procedures.

Outcome Time Frame:

3 years

Safety Issue:

No

Principal Investigator

DAVID TAIEB

Investigator Role:

Principal Investigator

Investigator Affiliation:

Assistance Publique Hopitaux De Marseille

Authority:

France: Ministry of Health

Study ID:

2008/09

NCT ID:

NCT00875407

Start Date:

February 2009

Completion Date:

Related Keywords:

  • Chromaffin-tissue Derived Tumors

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