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CompletedNCT00685789ADAPTUpdated Sep 29, 2011

Acupuncture With Deqi And Psychological Effects in Treatment of Bell's Palsy

An interventional study of acupuncture, deqi and acupuncture Non-manipulation in Bell's Palsy, sponsored by Huazhong University of Science and Technology. Completed at 1 site in China. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2011-09-29.

Sponsored by Huazhong University of Science and Technology · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
355
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
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Study summary

The purpose of this study is to observe the influence of Deqi and neuropsychological factors on effects of acupuncture treatment for Bell's Palsy.

Read the detailed description

Through long-term clinical practice,acupuncture treatment on facial paralysis has been generally proved effective;the large number of ancient and modern medical literature also have suggested that acupuncture is beneficial for facial paralysis. However,a scientific basis is still needed to be established to make sure the efficacy of acupuncture be recognized internationally.This study will adopt a series of international practice scales ,such as House Brackmann Scale,Facial Disability Index(FDI),World Health Organization Quality of Life-BREF (WHOQOL-BREF), Cattell Personality Factors (16PF),and Cancellation test to evaluate the role of deqi and neuropsychological factors in the acupuncture treatment for Bell's Palsy.

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Conditions studied

  • Bell's Palsy

Keywords

  • Bell's palsy,deqi,acupuncture, neuropsychology
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In context

Bell Palsy

120 studies on the registry are indexed under Bell Palsy; 38 are open to participants now.

This study's enrollment of 355 is above the median of 50 across 93 interventional studies indexed under Bell Palsy.

Browse Bell Palsy studies →

Lead sponsor

Huazhong University of Science and Technology is the lead sponsor of 241 studies on the registry; 60 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patients who were diagnosed to have unilateral facial-nerve weakness without any identifiable causes within 168 hours after onset of symptoms;
  2. aged 18 to 65 years.

Exclusion criteria

Exclusion criteria:

  1. illiterate;
  2. the facial paralysis is caused by herpes zoster;
  3. recurrent facial paralysis;
  4. noticeable asymmetry of the face before the illness which may affect the evaluation;
  5. history of peptic ulcer disease, severe hypertension, uncontrolled diabetes, liver and kidney dysfunction, pregnancy, mental illness, or serious systemic diseases which may affect the treatment.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
355 participants (actual)

Study arms

  • Experimental
    Acupuncture with Deqi

    Needles were inserted and manipulated manually using the techniques such as lifting, thrusting, and twirling, until the internal compound sensation of soreness, numbness, fullness, aching, cool, warmth, heaviness and radiating sensation (Deqi) occurred. The needles were retained for 30 min.

    Device: acupuncture, deqi

  • Active comparator
    Acupuncture without Deqi

    Needles were simply inserted and retained for 30 min, without any other stimulation.

    Device: acupuncture Non-manipulation

Interventions

  • Deviceacupuncture, deqi

    Immediately after insertion of a needle, it is manually rotated backwards and forwards to induce the deqi sensation.

    Also known as: Manipulation

  • Deviceacupuncture Non-manipulation

    After insertion of a needle, no manipulation is applied, and the needle is retained for 30 minutes.

    Also known as: Non-Manipulation

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What researchers measure

Primary outcomes

  1. House-Brackmann scale (HBS)

    Time frame: 6 months after onset of symptoms

Secondary outcomes

  1. facial disability index (FDI)

    Time frame: 6 months after onset of symptoms

  2. World Health Organization Quality of Life-BREF(WHOQOL-BREF)

    Time frame: 6 months after onset of symptoms

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Study locations

1 site
  • Institute of Integrated Traditional Chinese and Western Medicine
    Wuhan, Hubei 430030, China
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References and documents

Publications

  • Xu SB, Huang B, Zhang CY, Du P, Yuan Q, Bi GJ, Zhang GB, Xie MJ, Luo X, Huang GY, Wang W. Effectiveness of strengthened stimulation during acupuncture for the treatment of Bell palsy: a randomized controlled trial. CMAJ. 2013 Apr 2;185(6):473-9. doi: 10.1503/cmaj.121108. Epub 2013 Feb 25. PubMed 23439629 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 29, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00685789
Lead sponsor
Huazhong University of Science and Technology
Collaborators
Hubei Hospital of Traditional Chinese Medicine, Wuhan No.1 Hospital, Xiangyang No.1 People's Hospital, Renmin Hospital of Wuhan University, Fudan University, Second Affiliated Hospital of Zhengzhou University, Yichang Hospital of Traditional Chinese Medicine, The First Hospital of Hebei Medical University, Wuhan General Hospital of Guangzhou Military Command
Responsible party
Wei Wang (Department of Neurology of Tongji Hospital, Huazhong University of Science and Technology) — Principal investigator
First posted
May 28, 2008
Start date
Oct 2008
Primary completion
Oct 2010
Completion
Dec 2010
Last update
Sep 29, 2011

Study contacts

Wei Wang, doctor
principal investigator · Tongji Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2008. You cannot join it, but the record below documents what was studied.

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