Enhanced Recovery After Surgery in Extremity Sarcoma

Part of paid clinical trials in Nashville, Tennessee.

Sponsor
Joshua Lawrenz
Study ID
NCT04461171
Status
Recruiting
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Conditions

  • Sarcoma

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Enhanced Recovery After Surgery — PROCEDURE
    Undergo an enhanced recovery after surgery program

Study Details

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.

Key Dates

Start date
Dec 14, 2020
Status verified
Jul 2024
Primary completion
Dec 31, 2025
Completion
Jun 30, 2026

Study Design

Enrollment
120 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT

Arms

  • Experimental: ERAS
    Administration of a perioperative non-narcotic, multimodal pain management pathway.
  • No Intervention: Non-ERAS (Conventional)
    Administration of a conventional perioperative pain management pathway that consists of both narcotic and non-narcotic pain medications.

Primary Outcome Measure

Pain scores [ Time Frame: 3 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Vanderbilt University Medical CenterNashvilleTennessee37232
Vanderbilt-Ingram Service for Timely Access
[email protected]
800-811-8480
Joshua M Lawrenz, MD (PRINCIPAL_INVESTIGATOR)

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By research site
Vanderbilt University Medical Center· Nashville, TN

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