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Clinical Trial Summary

Controlled clinical trial of two parallel groups, with random assignment 1:1, non-inferiority, blinded for the patient, for who administers the intervention and for who analyzes the data. 112 participants


Clinical Trial Description

Controlled clinical trial of two parallel groups, with random assignment 1:1, non-inferiority, blinded for the patient, for who administers the intervention and for who analyzes the data. 112 participants Outcomes: Primary: Numeric rating scale (NRS) ranging from 0 (no pain) to 10 (worst imaginable pain) was used for pain assessments daily for 15 days and subsequently monthly until completing 3 months. Co-primary: Assessment of symptomatology related to phantom limb pain daily for 15 days POP and subsequently monthly until completing 3 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05608733
Study type Interventional
Source Universidad de Antioquia
Contact Daniela González, Md
Phone 3122690961
Email daniela.gonzalezg@udea.edu.co
Status Not yet recruiting
Phase Phase 3
Start date December 2022
Completion date July 2025

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