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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01825967
Other study ID # 2013/532
Secondary ID
Status Not yet recruiting
Phase N/A
First received March 29, 2013
Last updated April 9, 2013
Start date April 2013
Est. completion date April 2014

Study information

Verified date April 2013
Source Corporacion Parc Tauli
Contact MORA L. LAURA, MD
Phone 34639101033
Email Lmora@tauli.cat
Is FDA regulated No
Health authority Spain: Ethics Committee
Study type Observational [Patient Registry]

Clinical Trial Summary

The management of acute diverticulitis maybe better if we have prognostic markers of evolution.

Hypothesis: C-reactive protein maybe a good prognostic marker of evolution of acute diverticulitis.

The investigators need to know the values of C-reactive protein to predict evolution of acute diverticulitis.


Description:

A prospective observational study. All the patients with TC-diagnosis of acute diverticulitis (AD) had a C-reactive protein (PCR) in the initial blood test.

The investigators will predict evolution of AD with the PCR initial.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Acute Diverticulitis

Exclusion Criteria:

- Other Abdominal Pathologies

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
C-reactive protein
measured C-reactive protein in all patients with acute diverticulitis

Locations

Country Name City State
Spain Corporacion Parc Tauli Sabadell Barcelona
Spain Corporacion parc tauli Sabadell Sabadell-Barcelona
Spain Corporacion Parc Tauli Sabadell Sabadell/barcelona
Spain Corporacion Parc Tauli Sabadell Sabadell/barcelona

Sponsors (1)

Lead Sponsor Collaborator
Corporacion Parc Tauli

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary C-Reactive Protein 24 Hours Yes
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