Efficacy of Enhanced Recovery After Surgery Pathway for Total Mastectomy
NCT ID: NCT03181139
Last Updated: 2017-06-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
386 participants
OBSERVATIONAL
2013-07-01
2016-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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pre-ERAS
Patients cared for prior to the implementation of the Enhanced Recovery after surgery for total mastectomy pathway
No interventions assigned to this group
post-ERAS
patients cared for after the implementation of the Enhanced Recovery after surgery for total mastectomy pathway. Pathway included preoperative acetaminophen and gabapentin, Pec blocks, multimodal analgesia postoperatively and aggressive PONV treatment.
ERAS pathway for Total Mastectomy
Enhanced Recovery after Surgery (ERAS) pathway for Total Mastectomy
Interventions
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ERAS pathway for Total Mastectomy
Enhanced Recovery after Surgery (ERAS) pathway for Total Mastectomy
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
FEMALE
No
Sponsors
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Mount Zion Health Fund
OTHER
Monica Harbell
OTHER
Responsible Party
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Monica Harbell
Assistant Professor
Other Identifiers
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ERASBreast
Identifier Type: -
Identifier Source: org_study_id
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