Enhanced Recovery After Surgery in Extremity Sarcoma
Purpose
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.
Condition
- Sarcoma
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
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
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Non-Randomized
- Intervention Model
- Sequential Assignment
- Intervention Model Description
- Two-group, prospective, consecutively enrolled, comparative non-randomized trial (N = 120) is to determine the feasibility and efficacy of implementing an enhanced recovery after surgery (ERAS) pain management pathway to patients undergoing surgical treatment for an extremity sarcoma.
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
Arm | Description | Assigned Intervention |
---|---|---|
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. |
|
Recruiting Locations
Nashville, Tennessee 37232
More Details
- Status
- Recruiting
- Sponsor
- Joshua Lawrenz
Detailed 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).