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Clinical Study and Mechanism of Far-infrared Acupoint Application on the Treatment of Cervical HR-HPV Infection

Clinical Study and Mechanism of Far-infrared Acupoint Application on the Treatment of Cervical HR-HPV Infection

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081478
Enrollment
Unknown
Registered
2024-03-01
Start date
2024-03-18
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

cervical high-risk human papilloma virus infection

Interventions

Treatment group:Use the patch during the non-menstrual period, paste the "far infrared acupoint paste" on the outside of Qugu acupoint underwear after taking a bath every night after menstruation is c
Control group:Use the patch during the non-menstrual period, paste the "comfort paste" on the outside of Qugu acupoint underwear after taking a bath every night after menstruation is clean, and change

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
21 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Patients with cervical HR-HPV infection. 2) Patients with pathologically diagnosed CIN grade I or less (including LSIL, mucosal inflammation, SPI, etc.). 3) Female patients aged between 21 and 65 with regular menstruation or menopause and sexual history. 4) Women whose body mass index (Body Mass Index,BMI) is within the normal range (18.5 = BMI < 24.0 kg/m2). 5) Patients did not participate in the clinical trial of other acupoints in the past 1 month, and did not use a patch similar to that of the experimental acupoint. 6) Patients who have no fertility requirements in the past half a year. 7) Patients who are willing to cooperate with the treatment follow-up and sign the informed consent form. 8) Researchers believe that patients are suitable to participate in clinical trials. 9) Patients without major organ diseases.

Exclusion criteria

Exclusion criteria: 1) Patients with acute infection of external genitalia, including candidal vaginitis, trichomonal vaginitis, chlamydia trachomatis infection and acute pelvic inflammatory disease. 2) Vaginal cleanliness IV degree. 3) lactating women and pregnant women. 4) Patients with systemic chronic consumptive diseases, severe cardiovascular diseases, liver and kidney diseases, and hematopoietic system diseases. 5) Patients with mental illness. 6) Patients who have a history of immune system and are using immunosuppressants. 7) Patients with a history of allergy or allergy to acupoint sticking.

Design outcomes

Primary

MeasureTime frame
HPV negative conversion rate;Pathological reversal rate;Changes of vaginal lavage fluid indexes (IL-2);Changes of vaginal lavage fluid indexes (IL-10);Changes of vaginal lavage fluid indexes (TNF- a);

Secondary

MeasureTime frame
Changes of clinical symptoms;

Countries

China

Contacts

Public ContactJing Xiao

Guangdong Provincial Hospital of Chinese Medicine

xiaojingson_2004@126.com+86 135 5614 8318

Outcome results

None listed

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