Enhanced Recovery After Surgery (ERAS) in Live Donor Kidney Transplant Recipients
Enrolling by invitation · Phase 4
Conditions studied: Postoperative Pain
In brief
The goal of this interventional study is to learn if an Enhanced Recovery After Surgery (ERAS) protocol works to reduce the need for narcotic pain medications in live donor kidney transplant recipients. The main questions it aims to answer are: Does the ERAS protocol lower the amount of opioid narcotic medication needed to manage post-surgery pain? Does the ERAS protocol help lower pain scores after surgery? Researchers will compare the ERAS protocol to previous patients where the ERAS protocol was not used to see if the ERAS protocol works to reduce post-surgery pain. Participants will be asked to: * Drink a pre-surgery carbohydrate drink two hours before your surgery. * Take a pre-surgery dose of Tylenol by mouth. * Take a pre-surgery dose of Gabapentin by mouth. * The surgeon will administer a local numbing medication at the surgery site by injection during the surgery. * Begin walking with assistance about 12 hours after your surgery. * Allow the research staff to collect data about your kidney function. This data will be collected on your postoperative clinic visits, which generally occur about twice weekly for one month. This information will determine your kidney health, need for hospitalization, and side effects that may occur.
Key facts
- Study ID
- NCT06997016
- Run by
- Baylor Research Institute
- People needed
- 60
- Starts
- 2025-05-05
- Expected to finish
- 2027-06-01
- Last updated by the study team
- 2026-01-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult patients
- over 18 years of age
- receiving a kidney transplant from a living donor.
You may not qualify if…
- delayed gastric emptying
- severe type I diabetes
- allergy to interventional medications
- pregnancy (this is a normal exclusion for kidney recipients)
Where it is running
- Baylor Scott & White All Saints Medical Center — Fort Worth, Texas, United States
Full record on ClinicalTrials.gov
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