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Clinical Study on the Effect of Fire Dragon Moxibustion Combined with Shi's Acupuncture in Treating Lumbar Disc Herniation of Wind-Cold Dampness Bi Syndrome

Clinical Study on the Effect of Fire Dragon Moxibustion Combined with Shi's Acupuncture in Treating Lumbar Disc Herniation of Wind-Cold Dampness Bi Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001360
Enrollment
Unknown
Registered
2026-05-26
Start date
2025-03-26
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Lumbar Disc Herniation

Interventions

Fire Dragon Moxibustion group:Fire Dragon Moxibustion
warm needle moxibustion group:warm needle moxibustion

Sponsors

Shi Ying
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meet the aforementioned diagnostic criteria for both Traditional Chinese Medicine (TCM) and Western medicine; (2) Voluntarily participate as a subject and sign the Informed Consent Form (ICF); (3) Age 40 to 80 years, with a disease duration of > 3 years, regardless of gender; (4) Visual Analogue Scale (VAS) pain score of 4 to 7 (inclusive); (5) Able to cooperate in completing the questionnaires and fully understand the meaning of all items in the scales.

Exclusion criteria

Exclusion criteria: Subjects meeting any of the following criteria will be excluded: (1) Uncontrolled systemic or local infections making them unsuitable for treatment; (2) Concomitant lumbar fracture, spina bifida, lumbar malignancy, or lumbar tuberculosis; (3) Diabetes or other conditions that may affect skin integrity and healing capacity; (4) Skin damage, scarring, or abnormal changes in local skin temperature at the test site; (5) Severe concurrent primary diseases affecting the cardiovascular, hepatic, renal, or hematopoietic systems; (6) Current participation, or participation within the past 1 month, in other clinical trials where the interventions may interfere with efficacy observation.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale, VAS;

Secondary

MeasureTime frame
Infrared thermography temperature;Oswestry Disability Index ;

Countries

China

Contacts

Public ContactShi Ying

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

shiying1974@126.com20256666

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 11, 2026