ClinicalTrials.Veeva

Menu

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

C

Chengdu PLA General Hospital

Status

Unknown

Conditions

Ankylosing Spondylitis

Treatments

Other: Weizhong and Huantiao
Other: A-shi point

Study type

Interventional

Funder types

Other

Identifiers

NCT02260310
BL40GB30

Details and patient eligibility

About

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.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

Weizhong and Huantiao
Experimental group
Description:
Patients with Ankylosing Spondylitis use the Acupuncture Protocol Involving in Weizhong (BL4) and Huantiao (GB30) Points
Treatment:
Other: Weizhong and Huantiao
A-shi point
Active Comparator group
Description:
Patients with Ankylosing Spondylitis use the Acupuncture Protocol Involving in A-shi points, without including Weizhong (BL4) and Huantiao (GB30) Points
Treatment:
Other: A-shi point

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems