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Clinical study on the painful effect of shock wave in patients with RA

Clinical study on the painful effect of shock wave in patients with RA

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063782
Enrollment
Unknown
Registered
2022-09-16
Start date
2022-09-16
Completion date
Unknown
Last updated
2023-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rheumatoid arthritis

Interventions

Group 1 :Shock wave
Group 2:MTX, Diclofenac

Sponsors

University Hospital Macau
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. The patient voluntarily signed the informed consent form for this trial; 2. For patients with RA, the NRS score is greater than 3; 3. MRI of the corresponding joints was performed to exclude bone marrow lesions, and the age was 18-65 years old; 4. No nerve block therapy was performed within 1 month before enrollment in this study.

Exclusion criteria

Exclusion criteria: 1. Treatment site infection, hematoma; 2. BP < 90/60 mmHg, HR < 50 beats/min; 3. Coagulation dysfunction; 4. Severe heart, lung, liver and kidney insufficiency; 5. Mental and psychological disorders, unable to clearly express the pain NRS score; 6. Participated in other clinical research within three months; 7. The researcher considers that any reason is unsuitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
NAV2 content;Numerical rating scale score;Patient Health Questionnaire-9, PHQ-9 score;Generalized Anxiexy Disorde-7, GAD-7 ;

Secondary

MeasureTime frame
Efficacy Evaluation Registration Form;

Countries

China

Contacts

Public ContactMei Zhang

University Hospital, MUST Foundation

meizhang@must.edu.mo+86 18165586565

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026