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NCT04684693 Clinical Trial

Effect of Laser Puncture on Rheumatoid Arthritis Patients

Rheumatoid Arthritis Clinical Trial

Official title:
Effect of Laser Puncture on Rheumatoid Arthritis Patients

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT04684693
Other study ID # REC/010-2020
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date December 25, 2020
Est. completion date January 22, 2021

Study information
Verified date December 2020
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Studying the effect of laser puncture on rheumatoid arthritis patients

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 60
Est. completion date January 22, 2021
Est. primary completion date January 20, 2021
Accepts healthy volunteers No
Gender All
Age group 65 Years to 75 Years
Eligibility Inclusion Criteria: - Meeting the criteria of ACR classification for rheumatoid arthritis - Meeting the criteria of EULAR classification for rheumatoid arthritis Exclusion Criteria: - Having malignancy - Having connective tissue disease - Smokers

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Laser
Laser puncture and exercise
Procedure:
• Control
Exercise

Locations
Country Name City State
Egypt M. Sedky Cairo

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary HAQ (Change) Health Assessment questionnaire Pre-intervention, 4 weeks
Primary RAQoL (Change) Rheumatoid Arthritis Quality of Life Pre-intervention, 4 weeks
Primary CRP (Change) Analysis of serum C-reactive protein Pre-intervention, 4 weeks
Primary IL-6 (Change) Plasma interleukin-6 inflammatory markers Pre-intervention, 4 weeks
Primary ATP (Change) Plasma ATP concentration anti-oxidant marker Pre-intervention, 4 weeks
Primary MDA (Change) plasma malondialdehyde oxidative marker Pre-intervention, 4 weeks
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