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TerminatedNCT00514332Updated Aug 9, 2007

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

An interventional study of stent in Colorectal Obstruction and Left Colonic Adenocarcinoma, sponsored by University Hospital, Montpellier. Terminated. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2007-08-09.

Sponsored by University Hospital, Montpellier · Not applicable, Interventional, and Treatment

Why this study was terminated
enrolling participants stopped
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

To evaluate wether colorectal stenting carry a significant clinical advantage

Read the detailed description

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

02

Conditions studied

  • Colorectal Obstruction
  • Left Colonic Adenocarcinoma

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Keywords

  • colorectal stents
  • colonic obstruction
  • colonic adenocarcinoma
  • colorectal surgery
03

In context

Adenocarcinoma

2,004 studies on the registry are indexed under Adenocarcinoma; 374 are open to participants now.

This study's enrollment of 70 is above the median of 45 across 1,553 interventional studies indexed under Adenocarcinoma.

Browse Adenocarcinoma studies →

Lead sponsor

University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • obstructive stenosis due to left colorectal cancer

Exclusion criteria

Exclusion Criteria:

  • previous colorectal cancer
  • other colorectal location
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
70 participants (actual)

Study arms

  • Experimental
    A

    primary surgery group

    Procedure: stent

Interventions

  • Procedurestent

    stent placement for colorectal cancer obstruction

    Also known as: self-expending metallic stents

06

What researchers measure

Primary outcomes

  1. number of stoma in each group

    Time frame: within the first 6 month(plus or minus 1 month) after surgery

Secondary outcomes

  1. mortality in each group

    Time frame: within the first 6 month (plus or minus 1 month) after surgery

  2. complications

    Time frame: within the first 6 month (plus or minus 1 month) after surgery

  3. number of procedures

    Time frame: within the first 6 month (plus or minus 1 month) after surgery

  4. length of stay

    Time frame: within the first 6 month (plus or minus 1 month) after surgery

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Pirlet IA, Slim K, Kwiatkowski F, Michot F, Millat BL. Emergency preoperative stenting versus surgery for acute left-sided malignant colonic obstruction: a multicenter randomized controlled trial. Surg Endosc. 2011 Jun;25(6):1814-21. doi: 10.1007/s00464-010-1471-6. Epub 2010 Dec 18. PubMed 21170659 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 9, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00514332
Lead sponsor
University Hospital, Montpellier
Collaborators
University Hospital, Rouen, University Hospital, Toulouse, University Hospital, Grenoble, Rennes University Hospital, University Hospital, Lille, University Hospital, Angers, University Hospital, Bordeaux
First posted
Aug 9, 2007
Start date
Dec 2002
Completion
Oct 2006
Last update
Aug 9, 2007

Study contacts

Bertrand L MILLAT, MD-PhD
principal investigator · University Hospital, Montpellier

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Aug 2007. You cannot join it, but the record below documents what was studied.

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