Enhanced Recovery Pathway for Endoscopy

Status Withdrawn

Clinical Trial Summary

The purpose of this study is to compare an Enhanced Recovery Pathway to the current pre-operative/recovery practices of the endoscopy department on patient post-procedure outcomes.

Clinical Trial Description

Every 4th to 5th patient that checks in to the endoscopy department for their procedure will be screened for eligibility requirements. If eligible for the study, the patient will be informed about the study and potential risks. All patients giving written informed consent will be enrolled into the enhanced recovery protocol (ERP) [nursing managed ERP: goal-directed fluid management (Lactated Ringer's Solution at 5mL/kg/hr), PONV prophylaxis for an apfel score of 2 or greater (ondansetron 4 mg IV), early mobilization up to chair (within 5-30 minutes of admission to the recovery room), and early PO intake within 15-30 minutes of admission to the recovery room post-procedure] for their procedure. ;

Study Design

Related Conditions & MeSH terms

Endoscopy

Clinical Trial Details

NCT number	NCT04983498
Study type	Interventional
Source	Northwestern University
Contact
Status	Withdrawn
Phase	Phase 4
Start date	September 1, 2021
Completion date	January 1, 2022

View Details

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