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NCT02260310 Clinical Trial

The Effect of Acupuncture Protocol Involving in Weizhong (BL4) and Huantiao (GB30) Points in Treating Ankylosing Spondylitis

Ankylosing Spondylitis Clinical Trial

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT02260310
Other study ID # BL40GB30
Secondary ID
Status Enrolling by invitation
Phase N/A
First received October 3, 2014
Last updated March 31, 2017
Start date October 2014
Est. completion date January 2018

Study information
Verified date March 2017
Source Chengdu PLA General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect of acupuncture protocol involving in Weizhong (BL4) and Huantiao (GB30) points in treating ankylosing spondylitis.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 100
Est. completion date January 2018
Est. primary completion date January 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Eligible adult (=18 years of age) patients

- had a diagnosis of AS for at least 3 months defined as definite by the 1984 modified New York criteria

- Eligible patients also had a Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) of =4 (0-10 cm scale)

- A visual analogue scale (VAS) score for total back pain of =4 (0-10 cm scale)

Exclusion Criteria:

- Had received prior Acupuncture therapy

- With complete ankylosis of the spine, defined as the presence of bridging syndesmophytes at all intervertebral levels of the cervical and lumbar spine on lateral view spinal radiographs

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Weizhong and Huantiao

• A-shi point

Locations
Country Name City State
China 270 Rongdu street, Jin-niu district,Rheumatology Center of Integrated Medicine, General Hospital of Chengdu Military Area Command PLA, Chengdu city Sichuan

Sponsors (1)
Lead Sponsor Collaborator
Chengdu PLA General Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change from Baseline in McGill Pain Questionnaire (MPQ) at 12 weeks At 0 week, 6 weeks, 12 weeks
Primary Change from Baseline in Visual Analog Scale at 12 weeks At 0 week, 6 weeks, 12 weeks
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