NCT00915044

Brief Summary

The purpose of this study is to examine the effects of different environmental factors on immune cells in patients with IBD.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2007

Completed
1.9 years until next milestone

First Submitted

Initial submission to the registry

June 3, 2009

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 5, 2009

Completed
5.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2014

Completed
Last Updated

June 5, 2009

Status Verified

June 1, 2009

Enrollment Period

7 years

First QC Date

June 3, 2009

Last Update Submit

June 4, 2009

Conditions

Keywords

IBD

Outcome Measures

Primary Outcomes (1)

  • Migration towards chemokines,proliferation, cytokine secretion, phenotypical characterization.

    Once, when joining the study

Study Arms (2)

IBD patients

Approximately 40 patients (adults and children) suffering from IBD will be enrolled.

Controls

Approximately 100 healthy controls

Eligibility Criteria

Age10 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adults and children aged 10-80. Research group: Approximately 40 patients (adults and children) suffering from IBD will be enrolled. Control group: Approximately 100 controls will be enrolled in the research.

You may qualify if:

  • IBD

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dep. of Gastroenterology, Tel Aviv medical center

Tel Aviv, Israel

RECRUITING

Biospecimen

Retention: SAMPLES WITHOUT DNA

15 ml peripheral blood will be obtained from all participants.

MeSH Terms

Conditions

Inflammatory Bowel Diseases

Condition Hierarchy (Ancestors)

GastroenteritisGastrointestinal DiseasesDigestive System DiseasesIntestinal Diseases

Study Officials

  • Iris Dotan, MD

    Tel-Aviv Sourasky Medical Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

June 3, 2009

First Posted

June 5, 2009

Study Start

July 1, 2007

Primary Completion

July 1, 2014

Last Updated

June 5, 2009

Record last verified: 2009-06

Locations