Improving recovery after surgery for extremity sarcoma
Official title: Enhanced Recovery After Surgery in Extremity Sarcoma
Run by Vanderbilt-Ingram Cancer Center · NCT04461171 · Data updated 2026-11-12
This study is testing a new recovery plan for people having surgery for extremity sarcoma to see if it helps them manage pain better and recover faster without using narcotics.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 120 (estimated) |
| Sponsor | Vanderbilt-Ingram Cancer Center Academic / other |
| Locations | 1 site (Nashville, Tennessee) |
| Status | Recruiting |
| Started | December 14, 2020 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | August 21, 2026 |
| Trial ID | NCT04461171 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adult patients over 17 years old who are undergoing surgical excision for suspected extremity sarcoma at Vanderbilt University Medical Center.
✕Probably not a fit
Patients who are treated non-operatively or are non-English speaking may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to evaluate the effectiveness of an enhanced recovery after surgery (ERAS) pathway for patients undergoing surgical treatment for extremity sarcoma. It focuses on implementing a non-narcotic, multimodal pain management approach during the perioperative period. Key outcomes will include patient-reported pain scores, limb function assessments, and clinical metrics such as hospital length of stay and opioid usage. The study will collect data on these endpoints to determine the overall impact of the ERAS protocol on recovery.
Why it matters
Potential benefit: If successful, this approach could lead to improved recovery experiences and outcomes for patients undergoing surgery for extremity sarcoma.
How similar studies have gone: Other studies have shown success with enhanced recovery protocols in various surgical contexts, suggesting potential for positive outcomes in this setting as well.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Any patient at Vanderbilt University Medical Center treated with surgical excision of a suspected extremity sarcoma * Adult patients \>17 years of age * Patients of all preoperative opioid status (naïve or dependent) Exclusion Criteria: * Patients treated non-operatively * Non-English speaking patients
Where it's running
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Vanderbilt University Medical Center
Nashville, Tennessee, United States Recruiting
Study contacts
- Principal investigator: Joshua Lawrenz, MD — Vanderbilt Medical Center
- Study coordinator: Vanderbilt-Ingram Service for Timely Access
- Email: cip@vumc.org
- Phone: 800-811-8480
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.