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Efficacy and Safety of Acupuncture Combined with Moxibustion under Deqi Mode for Asymptomatic Hyperuricemia: A Randomized Controlled Trial

Efficacy and Safety of Acupuncture Combined with Moxibustion under Deqi Mode for Asymptomatic Hyperuricemia: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001820
Enrollment
Unknown
Registered
2025-09-24
Start date
2025-09-29
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Asymptomatic Hyperuricemia

Interventions

Verum Acupuncture Group:Acupuncture :Selected Acupoints: Bilateral Fujie, Daheng, Yinlingquan, Zusanli, Fenglong, Taixi
Method: Needles are inserted to an appropriate depth until deqi is achieved. Moxibustion: Selected Acupoints: Bilateral Tianshu and Zusanli, Method: Moxa sticks are held 3–5 cm above the acupoint surf
Sham Acupuncture Group:Sham Acupuncture: Selected Acupoints: Same as real acupuncture. Method: Blunt-tip needles are placed on non-acupoint/non-meridian skin areas (without penetration) to simulate re

Sponsors

Puyang Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Participants must meet all of the following criteria: 1.Diagnostic Confirmation Fulfill the diagnostic criteria for asymptomatic hyperuricemia as defined in the 2023 Integrated Traditional Chinese and Western Medicine Guidelines for the Diagnosis and Treatment of Gout and Hyperuricemia Issued by:Chinese Society of Integrated Traditional and Western Medicine Drafted by:First Teaching Hospital of Tianjin University of Traditional Chinese Medicine 2.Age Range 18 to 70 years old (inclusive) 3. Informed Consent Voluntarily agree to participate in the study Willing to undergo all required examinations and treatments Provide written informed consent

Exclusion criteria

Exclusion criteria: Participants will be excluded if they meet any of the following conditions: 1. Gout History Previous diagnosis of gout (acute or chronic) 2. Poorly Controlled Comorbidities Type 2 diabetes with HbA1c =8.4% Uncontrolled hypertension )SBP =160 mmHg or DBP =100 mmHg) Other conditions known to disrupt uric acid metabolism 3. Organ Dysfunction Cardiovascular or cerebrovascular diseases with life-threatening risks Severe hepatic/renal impairment: Chronic kidney disease (CKD stage =2) Serum creatinine BUN ALT or AST levels >2× upper limit of normal 4. Special Populations Alcohol dependence (defined as >40 g/day ethanol for men >20 g/day for women) Pregnancy or lactation Psychiatric disorders 5. Hypersensitivity History of severe allergic reactions 6. Medication Interference Use of urate-altering drugs (e.g. allopurinol febuxostat probenecid) within 3 months prior

Design outcomes

Primary

MeasureTime frame
Number of patients with blood uric acid (UA) reaching target levels;

Secondary

MeasureTime frame
Serum Uric Acid (SUA) Changes;Blood Uric Acid (BUA) Target Achievement Rate?;Lipid Profile;Fasting Blood Glucose;Liver Function;Renal Function;Body Weight,Body Mass Index;Waist Circumference ,Hip Circumference;Blood Pressure;

Countries

China

Contacts

Public ContactWei Huina

Puyang Hospital of Traditional Chinese Medicine

13213916253@163.com13213916253

Outcome results

None listed

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