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Clinical Trials/NCT02326415
NCT02326415
Unknown
Not Applicable

Prospective Randomised Study Comparing Clinical Pathway With "Fast-Track" Versus Usual Protocol In Uncomplicated Acute Appendicitis

Hospital Universitario Virgen de la Arrixaca1 site in 1 country300 target enrollmentMay 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Uncomplicated Acute Appendicitis
Sponsor
Hospital Universitario Virgen de la Arrixaca
Enrollment
300
Locations
1
Primary Endpoint
Postoperative Hospital Stay
Last Updated
11 years ago

Overview

Brief Summary

The aim of this study is to reduce the postoperative hospital stay, without increasing morbidity and mortality postoperative, expressed in terms of rate of complications and readmissions.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
December 2016
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hospital Universitario Virgen de la Arrixaca
Responsible Party
Principal Investigator
Principal Investigator

Jesus Abrisqueta Carrion

Ph D

Hospital Universitario Virgen de la Arrixaca

Eligibility Criteria

Inclusion Criteria

  • Patients diagnosed with uncomplicated acute appendicitis urgently.
  • Signing the consent of participation and commitment to attend reviews.

Exclusion Criteria

  • Suspected liver disease.
  • Coagulation disorders.
  • Patients in septic shock.
  • Pregnant patients.
  • Patients with symptoms compatible with acute uncomplicated appendicitis (plastron appendix, perforated appendicitis or diffuse peritonitis), or had 5 to more days of evolution).
  • No sign consent for participation in it.

Outcomes

Primary Outcomes

Postoperative Hospital Stay

Time Frame: From the first moment after surgery within 3 months

Measure the time from when the patient leaves the operating room until discharge

Secondary Outcomes

  • Overall satisfaction (Study the degree of satisfaction that the patient has received assistance as)(From the first moment after surgery within 3 months)

Study Sites (1)

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