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Web-based International Register of Emergency Surgery and Trauma

ConditionsAcute AppendicitisAcute CholecystitisAcute DiverticulitisPost-operative ComplicationsAcute PancreatitisPerforated Gastro-duodenal UlcersAdhesive Small Bowell OcclusionColonic Neoplastic EmergenciesGynecological EmergenciesVascular EmergenciesIntestinal IschemiaAbdominal Wall HerniaForeign BodiesCaustic IngestionTrauma
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorA.O. Ospedale Papa Giovanni XXIII

About this trial

The WIRES-T project (Web-based International Registry of Emergency General Surgery and Trauma) has been set up to allow to all the EGS (Emergency General Surgery) and Trauma surgeons to register their activity and to obtain a worldwide register of traumatic and non traumatic surgical emergencies. This will give the opportunity to evaluate results on a macro-data basis and to give index allowing stratifying, evaluating and improving the outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients affected by an acute surgical disease

Patients with indication to be referred to the emergency surgeon attention

Patients to be operated or to be treated with non-operative approach without surgical intervention

Disqualifiers

Patients not affected by an acute surgical disease

Patients without indication to be referred to the emergency surgeon attention

Trial population

All patients affected by an acute surgical disease and/or who may require to be undergone to the emergency surgeon attention to be managed either with an operative or a non-operative approach.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Emergency General Surgery

    Procedure/Surgery

    Emergency General Surgery and Trauma operative/non operative management

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Rate of patients treated with surgery

Evaluate the rate of operative treatment for each different disease according to the different enviroment; for each intervention the surgical approach (laparotomic, mini-invasive, laparoscopic) will be evaluated.

Time frame
Until hospital discharge, approximately 2 weeks
2

Rate of patients treated with conservative treatment

Evaluate the conservative treatment rate for each different disease according to patient's characteristics and the enviroinment.

Time frame
Until hospital discharge, approximately 2 weeks

Secondary outcomes

1

Mortality

To evaluate the differences in mortality rate linked to the different managements, techniques, environments and patient variables.

Time frame
Until hospital discharge, approximately 2 weeks
2

Morbidity

To evaluate the differences in morbidity rate linked to the different managements, techniques, environments and patient variables.

Time frame
Until hospital discharge, approximately 2 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

A.O. Ospedale Papa Giovanni XXIII

Lead sponsor

University of Pisa

Sponsor institution

World Society of Emergency Surgery

Collaborator

University of Pisa

Collaborator

Source ClinicalTrials.gov
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