U.S., Oct. 22 -- ClinicalTrials.gov registry received information related to the study (NCT07887516) titled 'Nerve Block Resolution Time Display and Pain Complaints' on Oct. 09.
Brief Summary: This randomized prospective study will evaluate whether displaying the expected nerve block resolution time on a patient's splint reduces postoperative pain-related complaints after orthopedic surgery. Adults with a fracture who undergo surgery at the Medical University of South Carolina and receive a preoperative nerve block may be eligible. Participants will be randomly assigned to receive standard verbal communication alone or standard verbal communication plus a written display of the expected nerve block resolution time on the splint. The study ...