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Randomized double-blind parallel Controlled clinical trial of alongside acupuncture for sympathetic cervical vertebrasickness

Alongside acupuncture for sympathetic cervical vertebrasickness: A Randomized,Double-blind,Parallel, Placebo Controlled Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-14005397
Enrollment
Unknown
Registered
2014-10-21
Start date
2015-01-01
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

sympathetic cervical vertebrasickness

Interventions

1:alongside acupuncture
2:Placebo needle

Sponsors

Tianjin Binhai New Area Dagang hospital of traditional Chinese medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Participants will be included if they fulfil the following conditions: aged 20 to 60 years old; meeting the diagnosis standard of sympathetic cervical vertebrasickness; No serious heart, liver and kidney disease, outpatients that can cooperate to check and treatment; volunteered to join this research and signed the informed consent.

Exclusion criteria

Exclusion criteria: Patients with any of the following conditions will be excluded: Patients undergoing other acupuncture treatment; With severe complications, intolerance of acupuncture; Pregnant, planning a pregnancy or nursing mothers.

Design outcomes

Primary

MeasureTime frame
Sympathetic cervical spondylosis assessment;

Secondary

MeasureTime frame
Visual Analog Scales;Neck Disability Index;Global Assessment;

Countries

China

Contacts

Public ContactWeiguang Liu
glllwg1978@163.com+86 13821935038

Outcome results

None listed

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