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Life sciences · Interventional Study
ClinicalTrials.gov · October 8, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
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Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT06938581). This is a study registration, not published results. Lead sponsor: University of Nebraska. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 260 participants (ESTIMATED). Conditions: Breast Cancer, Postoperative Recovery. Interventions: OTHER: ERAS Protocol; OTHER: Standard Perioperative Care. Primary outcome measures: Proportion of Participants With Opioid Prescriptions Within 7 Days of Surgery , Within 7 days post-surgery; Immediate Post-operative Pain Score , Within 24 hours post-surgery. Brief summary: Enhanced Recovery After Surgery (ERAS) protocols have been of increasing interest in the surgical community for decades. The emphasis has been development of protocols to maximize pain control post-operatively without the use of opioids. While this approach has been studied extensively in the oncology surgery literature, little data exists on the utility of ERAS protocols in the setting of breast conserving surgery (BCS), which is a type of surgery to remove breast cancer while saving as much of the breast as possible. The purpose of this study is to determine the utility of implementing ERAS protocols in breast cancer patients undergoing breast conserving surgery. Study participants will be randomized to either ERAS protocol or standard peri-operative care without ERAS. The study will assess the how many opioid prescriptions are given in the first week after surgery and how much pain participants report right after surgery. Investigators will also look at how long participants stay in the recovery room and if medicine for nausea is needed.