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Observation on the clinical efficacy of floating needle combined with reperfusion activity in the treatment of pain caused by lumbar intervertebral disc protrusion

Observation on the clinical efficacy of floating needle combined with reperfusion activity in the treatment of pain caused by lumbar intervertebral disc protrusion

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000686
Enrollment
Unknown
Registered
2024-11-11
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lumbar disc herniation

Interventions

Control group:Before treatment, lifestyle guidance and education are provided. 14 sessions of electroacupuncture are given. After each electroacupuncture treatment, a massage therapy session is provid
Experimental group:Before treatment, lifestyle guidance and education are provided. The combined treatment of floating needle and reperfusion exercise is given twice, followed by 12 sessions of electr

Sponsors

Pujiang County Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for lumbar disc herniation with pain as the main symptom; (2) Aged between 20 and 50; (3) Those who have not undergone acupuncture and massage treatment for nearly 1 month; (4) Good compliance willing to cooperate with the study patients sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Pregnant and lactating women; (2) combined with serious primary diseases (such as cardiovascular hematopoietic and other diseases); (3) Persons with intellectual and mental disorders who cannot cooperate with treatment; (4) Allergic to needle metal medical tape medical alcohol and severe cicatricial constitution; (5) Patients with severe lumbar disc herniation such as severe osteoporosis lumbar fracture or slip; (6) Those who are participating in other clinical trials. Note: Subjects who meet any of the above criteria will be excluded.

Design outcomes

Primary

MeasureTime frame
Numeric Rating Scale;

Secondary

MeasureTime frame
Satisfaction and acceptance rating criteria: The total score is 100 the higher the score the higher the satisfaction and acceptance.;Compare the number of days required for pain relief of 70%.;

Countries

China

Contacts

Public ContactZheng Xiaohong

Pujiang County Hospital of Traditional Chinese Medicine

272371309@qq.com+86 18086823816

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026