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Comparison Between Colorectal Stents and Primary Surgery in Obstructive Colonic Cancer. A Randomized, Controlled Study

Etude Prospective Multicentrique randomisée Comparant Deux stratégies thérapeutiques Pour Les Cancers Coliques en Occlusion : stratégie Chirurgicale Exclusive Versus stratégie thérapeutique Avec Stent Colique Initial

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00514332
Enrollment
70
Registered
2007-08-09
Start date
2002-12-31
Completion date
2006-10-31
Last updated
2007-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Obstruction, Left Colonic Adenocarcinoma

Keywords

colorectal stents, colonic obstruction, colonic adenocarcinoma, colorectal surgery

Brief summary

To evaluate wether colorectal stenting carry a significant clinical advantage

Detailed description

Randomized controlled comparison between stents and primary surgery in obstructive left colonic obstructive carcinoma outside palliative situations.

Interventions

PROCEDUREstent

stent placement for colorectal cancer obstruction

Sponsors

University Hospital, Rouen
CollaboratorOTHER
University Hospital, Toulouse
CollaboratorOTHER
University Hospital, Grenoble
CollaboratorOTHER
Rennes University Hospital
CollaboratorOTHER
University Hospital, Lille
CollaboratorOTHER
University Hospital, Angers
CollaboratorOTHER_GOV
University Hospital, Bordeaux
CollaboratorOTHER
University Hospital, Montpellier
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* obstructive stenosis due to left colorectal cancer

Exclusion criteria

* previous colorectal cancer * other colorectal location

Design outcomes

Primary

MeasureTime frame
number of stoma in each groupwithin the first 6 month(plus or minus 1 month) after surgery

Secondary

MeasureTime frame
mortality in each groupwithin the first 6 month (plus or minus 1 month) after surgery
complicationswithin the first 6 month (plus or minus 1 month) after surgery
number of procedureswithin the first 6 month (plus or minus 1 month) after surgery
length of staywithin the first 6 month (plus or minus 1 month) after surgery

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026