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Clinical Effect of Long Round Needle

Z

Zhanqing Xie

Status

Completed

Conditions

Cervical Spondylotic Radiculopathy

Treatments

Procedure: Long round needle
Procedure: Filiform needle

Study type

Interventional

Funder types

Other

Identifiers

NCT05587075
HBaoding

Details and patient eligibility

About

The goal of this clinical trial is to test in the clinical effect of long round needle in the treatment of cervical spondylotic radiculopathy, and analyze its safety and its influence on pain and functional recovery. The main question it aims to answer is whether long round needle therapy for patients with cervical spondylotic radiculopathy is effective and safe. Participants will be selected as the research objects. They will randomly divided into control group (n = 49) and observation group (n = 49). The control group was treated with filiform needle, and the observation group was treated with long round needle. Researchers will compare the two groups to see the differences on the therapeutic effect, safety, Neck dysfunction index (NDI), pain score (McGill pain questionnaire, MPQ), quality of life (Generic Quality of Life Inventory-74, GQOL-74), and levels of inflammatory factors.

Enrollment

98 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

(1) meet the efficacy criteria for disease certificate diagnosis of Traditional Chinese medicine[4]In the category of "Arthralgia Syndrome" and "Stiff neck", the main diseases: numbness and pain in the shoulder, neck and upper limbs, secondary diseases: unfavorable neck movement, hard, heavy head, thin coating, reddish tongue; (2) cervical X-ray shows hyperplasia of the vertebral body; (3) the patient or family members are informed and signed consent.

Exclusion criteria

(1) patients with severe periarthritis of shoulder and mixed cervical spondylosis; (2) spinal canal space-occupying lesions and cervical spine tumors; (3) serious immune system diseases and infectious diseases; (4) liver and kidney insufficiency; (5) cardiovascular and cerebrovascular diseases; (6) mental diseases or medical history; (6) patients with incomplete clinical data and poor compliance.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

98 participants in 2 patient groups

Control group
Active Comparator group
Description:
The control group was treated with filiform needle.
Treatment:
Procedure: Filiform needle
Observation group
Experimental group
Description:
The observation group was treated with long round needle.
Treatment:
Procedure: Long round needle

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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