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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01155739
Other study ID # 141/08, Propéritonite
Secondary ID
Status Completed
Phase N/A
First received July 23, 2009
Last updated December 18, 2014
Start date June 2009
Est. completion date June 2014

Study information

Verified date December 2014
Source University of Lausanne Hospitals
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

Procalcitonin level used for determining length of antibiotic treatment in peritonitis and intra-abdominal infections. Hypothesis is that length of antibiotic use can be shortened by this method.


Description:

Prospective randomized trial


Recruitment information / eligibility

Status Completed
Enrollment 162
Est. completion date June 2014
Est. primary completion date June 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- More than 18 yo

- Patient requiring surgery for peritonitis or intra-abdominal infection following: perforation, necrosis, previous operation...

- Mannheim Peritonitis score > 14

- SIRS present

- Probability of survival > 72h

- Informed consent by patient/relatives

Exclusion Criteria:

- No SIRS

- Long date corticoid treatment

- Immunosuppression

- Thyroid medullary carcinoma

- Anaphylactic shock

- Acute hepatic deficiency

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland University Hospital of Lausanne Lausanne

Sponsors (1)

Lead Sponsor Collaborator
University of Lausanne Hospitals

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary antibiotic treatment length, hospitalisation length without antibiotic, infection recurrence, antibiotic cost at one month and during hospital stay Yes