Viewing Study NCT06345222



Ignite Creation Date: 2024-05-06 @ 8:21 PM
Last Modification Date: 2024-10-26 @ 3:25 PM
Study NCT ID: NCT06345222
Status: COMPLETED
Last Update Posted: 2024-04-04
First Post: 2024-03-28

Brief Title: Examining the Effect of Prolotherapy on Quality of Life and Painkiller Use in Patients With Knee Pain
Sponsor: Bursa Yüksek İhtisas Education and Research Hospital
Organization: Bursa Yüksek İhtisas Education and Research Hospital

Study Overview

Official Title: Examining the Effect of Prolotherapy on Quality of Life and Painkiller Use in Patients With Knee Pain
Status: COMPLETED
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 92 patients with a diagnosis of primary knee pain of unknown cause followed at the family medicine outpatient clinic and who met our exclusion criteria were invited to the study When creating patient list the examination of patients interviews with patients as well as their medical records and examinations were used Patients were divided into two groups prolotherapy n46 and control group n46 by simple randomization method However when the study started 32 people in the prolotherapy group and 33 people in the control group of these patients participated in the study Prior to the research detailed information was provided about the research in the experimental and control groups and signed consent was obtained from all participants that they volunteered to participate in the research 5 dectrose was applied to the prolotherapy group by injection method to the pain area In the control group existing medical treatments were continued and no injection procedure was performed Before the research all participants were evaluated with Case Report Form Visual Analog Scale VAS and Quality of Life Scale Short Form SF-36 The cases in the experimental and control groups were re-evaluated with the VAS and SF-36 scales at the first month
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None