Therapeutic effect of Fu's subcutaneous needling for shoulder pain: a randomized controlled trial

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000029641

Enrollment

Unknown

Registered

2020-02-08

Start date

2020-02-09

Completion date

Unknown

Last updated

2020-02-10

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

Conditions

shoulder pain

Interventions

Group A:Fu’s subcutaneous needling

Group B:conventional rehabilitation

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)Subjects with shoulder pain; 2) mentally intact that were able to follow; 3) no intracranial lesions evaluated by MRI; 4) no allergic to the ultrasound jel.

Exclusion criteria

Exclusion criteria: 1) shoulder pain induced by stroke assessed by MRI and physical examination, rotator cuff injury or subacromial bursitis by ultrasound check or heart disease; 2) severe cardiac, liver or kidney dysfunction that caused hospitalization in last 3 months.

Design outcomes

Primary

Measure	Time frame
shoulder mobility.;pressure pain;	—

Countries

China

Contacts

Public ContactXiao Bao

Yuebei People's Hospital

baoxiao1981@sina.com+86 13925136317

Outcome results

None listed

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