An Investigation of the effect of using a conformable and wearable ice pack on pain and discomfort following sacroiliac joint injection.

Not Applicable

• Conditions: Mechanical Sacroiliac joint dysfunction; Musculoskeletal - Other muscular and skeletal disorders

• Registration Number: ACTRN12622000554763
• Lead Sponsor: niveristy of Notre Dame Australia

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-04-11
• Last Update Posted: 19 April 2022

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

over age 18 and with the capacity to provide informed consent
Patients undergoing pre-determined sacroiliac joint injection

Exclusion Criteria

Inability to understand the Patient Consent and Information Form
Prior reaction to the use of cold therapies

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain scores on Numerical Rating Scale (NRS)[Baseline pre -injection, immediatley after injection, and at 24 hours post injection]

Secondary Outcome Measures

Name	Time	Method
Analgesic use by recording of tablets taken and at what time by the particpants [Baseline pre -injection, immediatley after injection, and at 4,8,12 ,24, 48 ,72and 96 ,hours post injection]