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Application of Combined Moxibustion and Acupuncture with Warm-Through-Meridian-Based Diagnosis and Comprehensive Cupping Therapy in Patients with Lumbar Disc Herniation

Application of Combined Moxibustion and Acupuncture with Warm-Through-Meridian-Based Diagnosis and Comprehensive Cupping Therapy in Patients with Lumbar Disc Herniation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113226
Enrollment
Unknown
Registered
2025-11-26
Start date
2024-08-01
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Lumbar Disc Herniation

Interventions

Control group:Standard acupuncture therapy was administered (primarily targeting local acupoints and Ashi points, supplemented by distal points along meridians
primary points included corresponding paravertebral points, Shenshu, Dàchángshu, Huántiào, Weizhong, and Yanglingquan
auxiliary points included Mìngmén and Yaoyángguan, using fine needles with balanced tonification and dispersion techniques). Acupuncture sessions were conducted once daily, with each course lasting 7
Observation Group:The intervention involved applying the Warming and Muscle-Releasing Cupping technique on top of the standard treatment regimen. Procedure: 1. Du Meridian Cupping: Patient in prone po

Sponsors

Weifang Medical University Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years 2. Meets Western medical diagnostic criteria for lumbar disc herniation and Traditional Chinese Medicine (TCM) diagnostic criteria for cold-damp obstruction pattern. 3. No other treatments that may affect efficacy assessment within 2 months prior to enrollment. 4.No history of lumbar trauma or surgery; no traumatic lumbar examinations within the past 6 months. 5. Intact skin at the procedure site, free of redness, swelling, scars, or lesions that may affect trial results. 6. Informed consent and voluntary participation in this study.

Exclusion criteria

Exclusion criteria: 1. Patients with clear surgical indications requiring surgical intervention. 2. Severe osteoporosis, or history of spinal tuberculosis, spinal tumors, etc. 3. History of major medical conditions such as severe cardiovascular disease, severe hypertension, coagulation disorders, etc. 4. Diabetic peripheral neuropathy or patients with sensory impairment in the limbs. 5. Pregnant women, women planning pregnancy, or lactating women. 6. Individuals with contact allergies or sensitivity to smoke. 7. Patients with psychiatric disorders or cognitive impairment who are unable to communicate effectively.

Design outcomes

Primary

MeasureTime frame
Back and leg pain;Lumbar function;Oswestry Dability Index;Clinical efficacy;

Countries

China

Contacts

Public ContactWang Jinrong

Weifang Medical University Affiliated Hospital

wjrwkl@126.com+86 135 6262 6836

Outcome results

None listed

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