Non-operative treatment of cervical dorsal rami entrapment syndrome: a randomized, control clinical trial

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IIR-15007565

Enrollment

Unknown

Registered

2015-11-27

Start date

2002-05-02

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

cervical dorsal rami entrapment syndrome

Interventions

2:drug

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: All the subjects had symptoms of neck, shoulder and/or upper limb pain. Those symptoms may accompany with headache, dizziness and/or hypesthesia of head and face.

Exclusion criteria

Exclusion criteria: Those with positive result (mostly cervical radiculopathy and myelopathy) of MRI or CT and who endured serious trauma within 2 weeks should also be excluded.

Design outcomes

Primary

Measure	Time frame
muscle power;	—

Countries

China

Contacts

Public ContactQi Li

drlee12@sjtu.edu.cn+86 18930174685

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 9, 2026