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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04474912
Other study ID # 6293-22-7-2020
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2020
Est. completion date November 29, 2020

Study information

Verified date November 2023
Source Zagazig University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The total number of the included subjects was 120 in 3 equal groups (RA, OA and control). All subject was subjected to serum IL17 level measurement. MSK US (of both wrists, MCPs, PIPs and DIPs) was done to all patients in RA and OA groups. Disease activity was measured by disease activity score (DAS28) for RA patients. Visual analogue scale for pain (VAS) was obtained from patients in RA and OA groups. Functional assessment was done using health assessment questionnaire (HAQ) for RA patients and the Australian/Canadian (AUSCAN) Osteoarthritis Hand Index for OA patients


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date November 29, 2020
Est. primary completion date November 29, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - A patient is considered having definite RA if he/she scores at least 6 points in the established classification system - A patient is considered having Hand OA if he /she Hand pain, aching, or stiffness plus 3 or 4 of hard tissue enlargement of 2 or more of 10 selected joints or hard tissue enlargement of 2 or more DIP joints or fewer than 3 swollen MCP joints, or deformity of at least 1 of 10 selected joints which are are the second and third distal interphalangeal (DIP), the second and third proximal interphalangeal, and the first carpometacarpal joints of both hands Exclusion Criteria: - Any subject with liver diseases, coronary artery diseases, kidney diseases or other inflammatory conditions was excluded from the study.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Zagazig University Faculty of Medicine Zagazig Sharqia

Sponsors (1)

Lead Sponsor Collaborator
Zagazig University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Other Radiologic bony changes in RA and OA patients During the whole course of the study period, recruited participants undergone musculoskeletal (MSK) ultrasound to assess the bony changes. 12 months
Primary Clinical disease activity in Rheumatoid Arthritis (RA) and hand Osteoarthritis (OA) patients During the whole course of the study, disease activity of the patients was measured by disease activity score (DAS28) for RA patients. Visual analogue scale for pain (VAS) was obtained from patients in RA and OA groups. Functional assessment was done using health assessment questionnaire (HAQ) for RA patients and the Australian/Canadian (AUSCAN) Osteoarthritis Hand Index for OA patients. 12 months
Secondary IL-17 serum levels in RA and OA patients IL-17 will be measured by enzyme linked immunosorbent assay from collected serum samples from the study participants 2 weeks