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Analysis of the effect of external shock and stimulated pain point on external humeral epicondylitis

Analysis of the effect of external shock and stimulated pain point on external humeral epicondylitis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045529
Enrollment
Unknown
Registered
2021-04-18
Start date
2021-04-19
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

External humeral epicondylitis

Interventions

Stimulated pain point therapy group:Dry needle trigger pain point therapy

Sponsors

The First Affiliated Hospital of Suzhou University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.It conforms to the diagnostic criteria of external humeral epicondylitis in the Pain Volume of Clinical Diagnosis and Treatment Guidelines compiled by Chinese Medical Association in 2007; 2.The patients who didn't take any midicine or receive any physicotherapy at last 2 weeks; 3.The numerical pain scale (NRS) was less than 7.

Exclusion criteria

Exclusion criteria: 1.The patients who is pregnant or prepared to pregnant; 2.The patients who participate in other clinincal trials within the last 3 months; 3.The patients who have received or are receiving other drugs or other treatment methods that affect the evaluation of efficacy within the last 3 months; 4.Patients with a history of cervical spondylosis (cervical fracture), frozen shoulder or affected limb nerve changes (e.g., carpal tunnel syndrome, etc.); 5.Showing signs of rheumatic or rheumatoid diseases; 6.A history of distal humerus or proximal forearm fractures; 7.The patients who suffered liver disease, kidney disease, cardiovascular disease,nervous system and cerebrovascular severe primary diseases, such as tuberculosis, joint deformity, tumor, mental illness or postoperation patients; 8.Patients who are critically ill and find it difficult to evaluate the efficacy and safety of treatment.

Design outcomes

Primary

MeasureTime frame
Numerical Pain Rating Scale;DASH Upper Limb Mobility Score;Mechanical Withdrawal Threshold;Cozen sign and Mill test;

Countries

China

Contacts

Public ContactWang Lina

The First Affiliated Hospital of Suzhou University

wangln@suda.edu.cn+86 13915400622

Outcome results

None listed

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