Viewing Study NCT06569615



Ignite Creation Date: 2024-10-26 @ 3:38 PM
Last Modification Date: 2024-10-26 @ 3:38 PM
Study NCT ID: NCT06569615
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-08-19

Brief Title: Efficacy of Extracorporeal Shock Wave Therapy LASER Therapy and Cryotherapy in Patients Having Sacroiliitis
Sponsor: None
Organization: None

Study Overview

Official Title: Efficacy of Extracorporeal Shock Wave Therapy LASER Therapy and Cryotherapy on PPT Pain and Functional Disability in Patients Having Sacroiliitis A Randomized Control Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This research aimed to determine the effect of extracorporeal shock wave therapy LASER therapy and cryotherapy on PPT Pain and functional disability in patients having Sacroiliitis
Detailed Description: The study will be based on a three-arm parallel group randomized control design sixty participants of sacroiliitis will be recruited from the Physiotherapy department at Najran University KSA Study objectives and procedure will be properly explained and written informed consent will be obtained at the beginning of the study All the participants will be randomly divided into three groups 1 2 and 3

All the participants in first week will receive the ice pack for 15 minutes 3 times a day at the lumbosacral area to reduce inflammation in the area along with rest to reduce irritation at the lumbosacral area for the first week

From the 2nd week

Group 1 will be administered ESWT plus exercise Group 2 will be administered LASER plus exercise and Group 3 will be administered cryotherapy and exercise

Study Oversight

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