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Clinical Trials/NCT03470870
NCT03470870
Unknown
Not Applicable

Nomogram Control of Predictive Factors of Early Withdrawal After Gynecologic Oncology Surgery in the Enhanced Recovery After Surgery (ERAS) Protocol and Assessment of Practices

Institut Paoli-Calmettes1 site in 1 country370 target enrollmentJanuary 8, 2018
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ConditionsGynecological Cancers

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gynecological Cancers
Sponsor
Institut Paoli-Calmettes
Enrollment
370
Locations
1
Primary Endpoint
Validation of a predictive nomogram of a short hospital stay (less than two days after surgery) on a prospective cohort of patients.
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Validation of a predictive nomogram of a short hospital stay (less than two days after surgery) on a prospective cohort of patients.

Detailed Description

* Validation of a predictive nomogram of short-term hospitalization (less than two days after surgery) * Analysis of the factors influencing the variations of average length of stay * Morbidity analysis of the ERAS program

Registry
clinicaltrials.gov
Start Date
January 8, 2018
End Date
February 8, 2020
Last Updated
8 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Institut Paoli-Calmettes
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •All patients who had surgery for gynecological cancer under the ERAS program.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Validation of a predictive nomogram of a short hospital stay (less than two days after surgery) on a prospective cohort of patients.

Time Frame: 2 days

Validation of a predictive nomogram of short-term hospitalization (less than two days after surgery)

Secondary Outcomes

  • Analysis of the factors influencing the variations of average length of stay.(1 day)
  • Description of the implementation of the ERAS program on the entire cohort.(1 day)
  • Descriptive analysis of the cohort.(1 day)
  • Analysis of the variation of the average duration of stay in time.(1 day)
  • Morbidity analysis of the ERAS program.(1 day)

Study Sites (1)

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