Geneva, Aug. 6 -- International Clinical Trials Registry received information related to the study (ChiCTR2600128999) titled 'The Effect of Showering Within 48-72 Hours After Percutaneous Kyphoplasty on Incision Infection, Pain, Comfort, and Patient Satisfaction: A Randomized Controlled Trial' on July 29.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: The Second Affiliated Hospital of Wenzhou Medical University
Condition:
osteoporotic vertebral compression fractures, OVCF
Intervention:
Delayed showering group (control group):Routine postoperative incision care
Recruitment Status: Not Recruiting
Phase: N/A
Date of First Enrollment: 2026-09-01
Target Sample Size: Delayed showering group (control grou...