Geneva, May 4 -- International Clinical Trials Registry received information related to the study (DRKS00039867) titled 'Preventing Nocebo Effects and Improving Compliance During the Removal of Transcutaneous K-Wires in the Outpatient Clinic Following Pediatric Osteosynthesis: A Pre-Post Intervention Study' on April 22.
Study Type: interventional
Study Design:
Allocation: Non-randomized controlled study
Masking: Blinded (masking used)
Control: Other
Assignment: other
Study design purpose: treatment
Primary Sponsor: Klinik St. Hedwig, Barmherzige Bruder Regensburg
Condition:
Pediatric Fractures
Intervention:
Group 1: Standard procedure for K-wire removal in the outpatient clinic. Monitoring via questionnaires (medical staff/parents...