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NCT Number: NCT06705322

Cnidium Monnieri Detoxification Formula for Persistent High-risk Human Papillomavirus Infection of Cervix.

The purpose of this study is to evaluate the clinical efficacy and safety of Cnidium Monnieri Detoxification Formula in clearing HPV infection, improving clinical symptoms and quality of life in female patients with persistent cervical high-risk HPV infection.

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Key information

About this study

Persistent infection with high-risk HPV is a major cause of cervical cancer and has negative psychosocial effects on women's health-related quality of life (QOL). This prospective, single-arm, multicenter study is to evaluate the clinical efficacy and safety of Cnidium Monnieri Detoxification Formula in clearing HPV infection, improving clinical symptoms and quality of life in female patients with persistent cervical high-risk HPV infection.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 25 years to ≤ 75 years,with sexual life history
  • Meet the diagnostic criteria for high-risk human papillomavirus (HR-HPV) persistent infection
  • After surgery or physical therapy for high-grade squamous intraepithelial lesions (HSIL) of the cervix or high-grade squamous intraepithelial lesions (VaINIII) of the vagina, or radical surgery for cervical/vaginal cancer or radical chemoradiotherapy, the examination remained positive for HR-HPV ≥6 months after the end of treatment, with the same type or multiple types as before treatment, and no progression or recurrence of the disease.
  • No local or systemic therapy has been administered to patients in the last 3 months
  • Patients were informed of the study protocol, agreed to cooperate with the treatment, and signed informed consent.

Exclusion criteria

  • Only low-risk HPV infection
  • Colposcopy for high-grade intraepithelial lesions or cancer of the cervix, vagina, vulva, who have not received or are receiving treatment
  • Immunocompromised or immunosuppressant
  • Pregnant and lactating women
  • Patients with other malignant tumors not controlled, serious heart, lung, liver, renal insufficiency and coagulation dysfunction
  • People with communication or cognitive impairment
  • Patients have contraindications to oral administration of traditional Chinese medicine preparations
  • In the same period, other anti-HPV measures were used to treat, which affected the efficacy judgment

Treatment and study plan

Cnidium Monnieri Detoxification Formula

Drug

Drug composition of Cnidium Monnieri Detoxification Formula: snake seed 9g, Tuckaia 30g, Matrine 9g, snake berry 30g, white Ying 30g. Based on the Cnidium Monnieri Detoxification Formula, the other symptoms were treated with syndrome differentiation and flavor. The traditional Chinese medicine decoction is provided by the Pharmacy of Yueyang Hospital of Integrated Traditional Chinese and Western Medicine Affiliated to Shanghai University of Traditional Chinese Medicine, with 1 dose per day, decocted into 300ml by a medicine decocter, packed in 2 vacuum bags, taken orally after meals, twice a day, one bag each time. Do not stop taking decoction during menstruation. 1 month is a course of treatment, at least 3 courses of treatment, no more than 6 courses of treatment.

Baseline HPV clearance, improvement in clinical symptoms and quality of life, and drug safety were assessed at 3 months, 6 months, and 12 months after initiation of treatment.

Primary outcomes

  1. Baseline HPV clearance at 6 months after treatment

    Time frame: 6 months

    HPV clearance rate at 6 months after treatment

Secondary outcomes

  1. Baseline HPV clearance at 12 months after treatment

    Time frame: 12 months

    HPV clearance rate at 12 months after treatment

  2. Safety

    Time frame: 6 months

    Proportion of adverse events within 6 months of treatment

Study contacts

Contact information is provided by the study sponsor or research team.

Tingyan Shi

CONTACT

[email protected]

86-21-64041990 ext. 2801

Sponsors and collaborators

Lead sponsor

Fudan University

Other

Registry information

Official study title

A Phase II, Multicenter Study on the Clinical Effectiveness of Cnidium Monnieri Detoxification Formula for Persistent High-risk Human Papillomavirus Infection of Cervix.

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Nov 26, 2024
Registry last updated
Nov 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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