Type of Study:

Interventional

Study Design:

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Outcome Measure:

Determination of the distance between a rectal tumor and the pouch of Douglas

Outcome Description:

Feasability of the determination of the distance between a rectal tumor and the pouch of Douglas by MR saline peritoneography: Visualisation of the Douglas Visualisation of the Tumor Determination of the distance between the tumor and the pouch of Douglas

Outcome Time Frame:

Two years

Safety Issue:

No

Principal Investigator

Cristina A Dragean, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Cliniques Universitaires St Luc - Université Catholique de Louvain

Authority:

Belgium: Institutional Review Board

Study ID:

B403201112604

NCT ID:

NCT01497457

Start Date:

December 2011

Completion Date:

March 2013

Related Keywords:

• Rectal Adenocarcinoma
• Adenocarcinoma
• Adenocarcinoma, Mucinous
• Rectal Neoplasms