Prospective Evaluation of Spleen Injury Treatments in Languedoc Roussillon

Prospective Evaluation of Spleen Injury Treatments in Languedoc Roussilon, France

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01103999

Enrollment

Registered

2010-04-15

Start date

2010-05-31

Completion date

2013-05-31

Last updated

2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Trauma

Keywords

spleen

Brief summary

Descriptive, prospective, multicenter evaluation of spleen injury treatment in the Languedoc Roussilon region according to trauma severity, morbi-mortality and length of hospitalization.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

16 Years to No maximum

Healthy volunteers

Inclusion criteria

* Hospitalized for abdominal trauma * diagnosis of splenic contusion confirmed by scanner or during surgery for hemodynamically unstable cases * patient has signed a consent form * patient is a beneficiary of or affiliated with a social security program

Exclusion criteria

* Refuses to participate * Pregnant or breastfeeding * Patient under guardianship

Design outcomes

Primary

Measure	Time frame	Description
Number of deceased participants	1 year	Mortality

Secondary

Measure	Time frame	Description
Number of participants with certain morbidities	3 months of follow up	The occurrence of pulmonary, thrombo-embolic, hemorrhagic, pancreatic, splenic and infectious morbidities are recorded.
Days in hospital	1 year of follow up	—
Direct costs (euros per patient)	1 year of follow up	Costs are calculated as a function of hospitalisation, surgical procedures, interventional radiology.

Countries

France

Outcome results