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Clinical Trial Summary

The purpose of this study is to demonstrate the efficacy of implementing the enhanced recovery after surgery (ERAS) pathway in a prospective manner to patients undergoing surgical treatment for extremity sarcoma.


Clinical Trial Description

Specifically, the focus of this study will be regarding the administration of a perioperative non-narcotic, multimodal pain management pathway. Primary endpoints collected with be short-term patient reported outcomes (pain scores [PROMIS] and [QoR-15]), limb function scores [MSTS], and key clinical outcomes (hospital length of stay, opioid requirements/prescribing data and perioperative complications). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04461171
Study type Interventional
Source Vanderbilt-Ingram Cancer Center
Contact Vanderbilt-Ingram Service for Timely Access
Phone 800-811-8480
Email cip@vumc.org
Status Recruiting
Phase N/A
Start date December 14, 2020
Completion date June 2025

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