Acute Diverticulitis and C-Reactive Protein as a Prognostic Marker
Predictive Value of C-Reactive Protein in Acute Diverticulitis
1 other identifier
observational
30
1 country
4
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Apr 2013
Shorter than P25 for all trials
4 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 29, 2013
CompletedStudy Start
First participant enrolled
April 1, 2013
CompletedFirst Posted
Study publicly available on registry
April 8, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2014
CompletedApril 10, 2013
April 1, 2013
1 year
March 29, 2013
April 9, 2013
Conditions
Outcome Measures
Primary Outcomes (1)
C-Reactive Protein
24 Hours
Study Arms (1)
Acute Diverticulitis
We measured C-reactive protein in all the patients diagnosed with acute diverticulitis
Interventions
measured C-reactive protein in all patients with acute diverticulitis
Eligibility Criteria
All Patients with Acute Diverticulitis
You may qualify if:
- Acute Diverticulitis
You may not qualify if:
- Other Abdominal Pathologies
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (4)
Corporacion Parc Tauli
Sabadell, Barcelona, 08208, Spain
Corporacion parc tauli
Sabadell, Sabadell-Barcelona, 08208, Spain
Corporacion Parc Tauli
Sabadell, Sabadell/barcelona, 08208, Spain
Corporacion Parc Tauli
Sabadell, Sabadell/barcelona, 08208, Spain
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
MORA LAURA, MD
Corporacion Parc Tauli
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Target Duration
- 30 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- General Surgeon
Study Record Dates
First Submitted
March 29, 2013
First Posted
April 8, 2013
Study Start
April 1, 2013
Primary Completion
April 1, 2014
Study Completion
April 1, 2014
Last Updated
April 10, 2013
Record last verified: 2013-04