acupuncture
DeviceThe needles will be inserted in acupoints through adhesive pads. Needles will be lifted, thrusted and twirled gently for 3 times to achieve deqi sensation and manipulated every ten minutes.
NCT Number: NCT07150234
This study will be an evaluation of the efficacy and safety of acupuncture for cervical spondylotic radiculopathy. The main questions it aims to answer are 1. Does acupuncture improve the pain intensity among patients with cervical spondylotic radiculopathy? 2. Does acupuncture treat cervical spondylotic radiculopathy safely? Researchers will compare acupuncture to sham acupuncture to see if acupuncture could improve symptoms among patients with cervical spondylotic radiculopathy. Experimental and control groups will be treated with 6 weeks of acupuncture or sham-acupuncture respectively. Patients were followed up at 1 month, 3 months, 6 months after treatment to record outcome, any disease progression, adverse events, and so on.
Trial opening soon.
Get Notified18 year–75 year
All sexes
Interventional
Not applicable
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The needles will be inserted in acupoints through adhesive pads. Needles will be lifted, thrusted and twirled gently for 3 times to achieve deqi sensation and manipulated every ten minutes.
The needles will be inserted into the pad and reaching the skin. Needles will be lifted, thrusted and twirled gently for 3 times to simulate the effect of the needle tip penetrating the skin.
Time frame: At 6 weeks from randomization.
Average NRS (numerical rating scale) score of arm pain decreased by at least 30% compared with baseline in the past 24 hours.
Time frame: At 1,3,6,10,18,30 weeks from randomization.
Time frame: At 1,3,6,10,18,30 weeks from randomization.
Time frame: At 1,3,10,18,30 weeks from randomization.
NRS (numerical rating scale) score of arm pain decreased by at least 30% compared with baseline in the past 24 hours.
Time frame: At 1,3,6,10,18,30 weeks from randomization.
NRS (numerical rating scale) score of neck pain decreased by at least 30% compared with baseline in the past 24 hours.
Time frame: At 3,6,10,18,30 weeks from randomization.
Time frame: At 3,6,10,18,30 weeks from randomization.
Time frame: At 1,3,6,10,18,30 week from randomization.
Time frame: At 6,10,18,30 weeks from randomization.
Time frame: At 3,6,10,18,30 weeks from randomization.
Time frame: At 3,6,10,18,30 weeks from randomization.
Time frame: At 6,10,18,30 weeks from randomization.
Time frame: At 6,30 weeks from randomization.
1 means great improvement of arm pain, 2 means moderate improvement of arm pain, 3 means better of arm pain, 4 means no change of arm pain, 5 means slight deterioration of arm pain, 6 means moderate deterioration of arm pain and 7 means much deterioration of arm pain.
Time frame: At 1,3,6,10,18,30 weeks from randomization.
Time frame: At 1,3,6,10,18,30 weeks from randomization.
Time frame: At 1,3,6,10,18,30 weeks from randomization.
Collect the adverse reactions related to acupuncture, such as needle breakage, local hematoma, infection and abscess, and any unexpected symptoms, signs or health conditions during the experiment.
Time frame: Baseline assessment (week 0)
Participants will be asked: Do you think your cervical spondylotic radiculopathy may be helped by acupuncture?
Time frame: Within 5 minutes after either treatment at week 6.
Participants will be asked: Do you think you have received traditional acupuncture in the past 6 weeks?
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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