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A study on the clinical efficacy and mechanism of acupoint embedding thread therapy for high-risk HPV infection based on the "psychoneuroimmunometabolic axis"

A study on the clinical efficacy and mechanism of acupoint embedding thread therapy for high-risk HPV infection based on the "psychoneuroimmunometabolic axis"

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000700
Enrollment
Unknown
Registered
2026-03-24
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Cervical HPV infection

Interventions

Acupoint Insertion Thread Group:Carry out acupuncture thread implantation
The fake acupoint embedding thread group:The group that underwent fake acupuncture thread insertion

Sponsors

The Obstetrics & Gynecology Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Visited Fudan University Affiliated Obstetrics and Gynecology Hospital from December 2025 to December 2026. 2. Diagnosed with persistent high-risk HPV infection in the cervix. Defined as: In women who have not been infected with the relevant HPV subtype before, the same HPV DNA subtype was detected for more than 2 consecutive times within a 12-month interval. 3. TCT test results were NILM or ASC-US or LSIL; and the results of the colposcopy examination conducted before enrollment were satisfactory, and no signs of suspected HSIL or more severe lesions were observed under the microscope. 4. The subjects voluntarily joined this study, signed the informed consent form, had good compliance, and cooperated with the follow-up. 5. Age = 18 years and = 70 years, with sexual life. 6. Agreed to follow the protocol of this study and practice effective contraception during the trial participation.

Exclusion criteria

Exclusion criteria: 1. The histopathological diagnosis is HSIL or above in the cervix, vagina, and vulva; 2. There are severe organ function disorders or complications; 3. Pregnant or having fertility requirements within the past half year; 4. Patients with hematological disorders or bleeding disorders; 5. Patients with acute inflammation of reproductive organs; 6. Patients with mental disorders; 7. Allergy to sutures; 8. Skin damage or infection at the suture site; 9. Patients with immune disorders; 10. Patients with severe heart disease or diabetes; 11. Patients who have had suture treatment before; 12. Those who have used glucocorticoids or immunosuppressants within the past 3 months; 13. Those who have received HPV vaccine within the past 6 months.

Design outcomes

Primary

MeasureTime frame
The clearance rate of HR-HPV and viral load;

Secondary

MeasureTime frame
Resting-state heart rate variability;Local immune indicators of the cervix;Peripheral blood immune system;metabolic index;Psychological state and sleep indicators;security index;

Countries

China

Contacts

Public ContactXin weijuan

The Obstetrics & Gynecology Hospital of Fudan University

xinwj80@126.com13795425780

Outcome results

None listed

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