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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02445690
Other study ID # USP
Secondary ID
Status Recruiting
Phase N/A
First received May 12, 2015
Last updated May 11, 2016
Start date May 2015
Est. completion date April 2017

Study information

Verified date May 2015
Source University of Sao Paulo General Hospital
Contact Andre ZA Leite, MD
Phone +551130617279
Email azaleite@gmail.com
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Observational [Patient Registry]

Clinical Trial Summary

One hundred and fifty patients with Crohn's disease involving the terminal ileum or the colon, in clinical remission, with or without endoscopic activity will be included. Thrombin generation will be measured and correlated with the simplified endoscopic activity score. The patients will be evaluated for development of deep vein thrombosis after one-year of follow-up.


Description:

One hundred and fifty patients with Crohn's disease involving the terminal ileum or the colon, in clinical remission defined by the Crohn's Disease Activity Index below 150 and Harvey-Bradshaw Index below 5, with or without endoscopic activity defined by simplified endoscopic activity score for Crohn's disease (SES-CD) will be included in this study (75 patients with a complete mucosal healing defined by SES-CD below 3 and 75 with endoscopic activity defined by SES-CD above 6) in multiple centers specializing in the treatment of inflammatory bowel diseases in Brazil; Study data will be collected and managed using REDCap electronic data capture tools hosted at the Clinical Hospital of University of São Paulo. REDCap (Research Electronic Data Capture) is a secure, web-based application designed to support data capture for research studies. All thrombin generation tests will be performed at the Clinical Hospital of University of São Paulo, São Paulo, SP through automatically calibrated Thrombogram (CAT- Calibrated Automated Thrombogram®, Maastricht, The Netherlands), with and without thrombomodulin. Those patients will be followed for at least one year after the colonoscopy with measurement of the D-dimer and clinical evaluation every 3 months to verify the developing of deep vein thrombosis.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date April 2017
Est. primary completion date April 2017
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Established Crohn's disease diagnosis for at least 6 months

- Disease involvement of the terminal ileum and/or colon

- Clinical remission

- Stable treatment for at least 3 months

Exclusion Criteria:

- Colectomy

- Neoplasia

- Surgery in the last 6 months

- Anticoagulant treatment

- Major liver disease

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Brazil Faculdade de Medicina de Botucatu -UNESP Botucatú SP
Brazil Universidade do Vale do Itajaí-UNIVALI / Santa Catarina Itajaí Santa Catarina
Brazil Clinical Hospital of São Paulo University São Paulo SP

Sponsors (2)

Lead Sponsor Collaborator
University of Sao Paulo General Hospital Fundação de Amparo à Pesquisa do Estado de São Paulo

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation between thrombin generation and endoscopic activity At the moment of the inclusion No
Secondary Association of a high thrombin generation and development of deep vein thrombosis After 1 year of follow up No
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