A Efficacy and Safety Study of Composite Gel Containing Black Raspberry Extract in Removing HPV From Patients With Cervical Intraepithelial Neoplasia(CIN) After Cervical Conization

Phase 2

• Conditions: HPV; Cervical Intraepithelial Neoplasia
• Interventions: Biological: Composite Gel Containing Black Raspberry; Biological: placebo

• Registration Number: NCT03745846
• Lead Sponsor: Tianjin Medical University Cancer Institute and Hospital

Brief Summary

To evaluate the efficacy and safety of composite gel containing black raspberry extract in removing HPV From patients With cervical intraepithelial neoplasia(CIN) after cervical conization

Detailed Description

A large number of basic research and animal experiments have confirmed that black raspberry and its active ingredients are used for chemo-prevention of tumors. In recent years, it has been reported that black raspberry extract can effectively inhibit the proliferation of human oral cancer cells and colorectal cancer cells and promote its apoptosis. At the same time, studies have found that chemically modified lactoglobulin exhibits highly potent antiviral activity against human papillomavirus (HPV) infection, including HPV6, HPV16 and HPV18, and can be used as an effective and safe antiviral drug for treatment and Prevent HPV infection. This study attempts to apply black raspberry and lactoglobulin to remove HPV virus and prevent cervical cancer, in order to make breakthroughs in the prevention and control of cervical cancer.

Study Timeline

• Status Verified: 2018-11
• Study First Submitted: 2018-11-13
• Study First Submitted QC: 2018-11-15
• Last Update Submitted: 2018-11-15
• Study First Posted: 2018-11-19
• Last Update Posted: 2018-11-19
• Study Start: 2018-12
• Primary Completion: 2019-08
• Study Completion: 2019-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 78

Inclusion Criteria

• Subjects were able and willing to sign informed consent.
• Patients with CIN who underwent cervical conization were at high risk of persistent HPV infection.
• Age must be between 20-55 years old.
• Subjects should begin receiving protocol studies at least two months after cervical conization.
• Patients must be readily available for study and follow-up.
• Patients should not participate in other clinical trials at the same time and agree not to participate in other interventional clinical trials during the protocol study. Except for questionnaires or observational studies.
• Patients should have appropriate nutritional status: body mass index BMI ≥ 18 kg / m2, body weight > 40 kg, serum albumin ≥ 3 g / dL.

Exclusion Criteria

Anyone who meets any of the following criteria is not allowed to participate in this test:

• Pregnant women, pregnant and lactating women.
• Patients who participated in other clinical trials in the past 3 months.
• It has a serious primary disease such as cardiovascular and cerebrovascular, hematopoietic system and liver and kidney, or patients with mental illness.
• Allergic patients.
• People with epidemics such as AIDS.
• Suffering from uncontrolled complications, including but not limited to: persistent or active infection; clinically significant healing or non-healing wounds; symptomatic congestive heart failure; unstable angina; clinically significant arrhythmia; A disease that affects research compliance, such as an infectious disease or a mental illness/social condition.
• Active, uncontrolled bacterial, viral or fungal infections and require systemic treatment.
• The patient has a history of other malignancies or is suffering from malignant tumors and autoimmune diseases.
• Have any active disease that may increase the risk of a program study or impair a patient's ability to receive protocol research.
• Patients who plan to stay on vacation for 14 days or more during the study period.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Composite Gel Containing Black Raspberry	Composite Gel Containing Black Raspberry	Drug:Composite Gel Containing Black Raspberry 3,000mg Dosage and duration: 1 preparation every other day for 3 months.
Composite Gel Containing Black Raspberry-placebo	placebo	Drug:Composite Gel Containing Black Raspberry-placebo 3,000mg Dosage and duration: 1 preparation every other day for 3 months.

Primary Outcome Measures

Name	Time	Method
negative rate	3 months	the effective rate and clearance rate of HPV infection from baseline as compared to placebo

Secondary Outcome Measures

Name	Time	Method
Adverse Events	3 months	The Rate of Solicited Adverse Events and the Related Features
recurrence rate	3 months	The recurrence rate after HPV clearance was assessed