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WithdrawnNCT01293656Updated Jun 2, 2015

Study of Participants With Crohn's Disease and Ulcerative Colitis in Eastern Europe, Middle East, and North Africa (P08166)

An observational study in Inflammatory Bowel Disease, Crohn's Disease and Ulcerative Colitis, sponsored by Merck Sharp & Dohme LLC. Withdrawn. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-06-02.

Sponsored by Merck Sharp & Dohme LLC (part of Merck & Co., Inc) · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
0
Ages
18 Years and older
Sex
All
01

Study summary

This study is being done to assess the clinical course and treatment options for Crohn's Disease (CD) and ulcerative colitis (UC) in the populations of Eastern Europe, Middle East, and North Africa.

02

Conditions studied

03

In context

Colitis

1,073 studies on the registry are indexed under Colitis; 131 are open to participants now.

Browse Colitis studies →

Lead sponsor

Merck Sharp & Dohme LLC is the lead sponsor of 2,114 studies on the registry; 132 are open to participants now.

Of its 489 completed or terminated interventional studies of FDA-regulated products, 362 (74%) have results posted.

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
Sampling method
Non-probability sample

Study population

All patients with CD or UC who visit the study sites in Eastern Europe, Middle East, and North Africa during the study period will be asked to participate.

Eligibility criteria

Inclusion Criteria:

  • Confirmed diagnosis of Crohn's disease or ulcerative colitis.
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
0 participants (actual)
Patient registry
No

Groups and cohorts

  • CD and UC participants

    All participants with CD or UC visiting their physician over a period of one year, newly and already diagnosed, regardless of treatment pattern.

    Other: No intervention.

Interventions

  • OtherNo intervention.

    There is no study intervention. Participants will be treated locally per site standards.

06

What researchers measure

Primary outcomes

  1. The number of participants with Crohn's Disease (CD) or ulcerative colitis (UC) who visit the participating sites.

    Time frame: 1 Year

  2. The number of participants with different degrees of CD and UC severity.

    Time frame: 1 Year

  3. Use rates of classes of drug therapy.

    Time frame: 1 Year

  4. Number and types of surgical interventions.

    Time frame: 1 Year

  5. Outcomes of surgical intervention.

    Time frame: 1 Year

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 2, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01293656
Responsible party
Sponsor
First posted
Feb 10, 2011
Start date
Aug 2011
Primary completion
Jul 2012 (estimated)
Completion
Jul 2012 (estimated)
Last update
Jun 2, 2015

Oversight

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

Not currently enrolling

This study is withdrawn, as verified in Jun 2015. You cannot join it, but the record below documents what was studied.

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