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Methylene Blue Injection for Nonneoplastic Epithelial Disorders of Vulva (NNEDsMB)

Primary Purpose

Nonneoplastic Epithelial Disorders of Vulva

Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
mixed methylene blue compound injection
Sponsored by
Maternal and Child Health Hospital of Hubei Province
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nonneoplastic Epithelial Disorders of Vulva focused on measuring Nonneoplastic Epithelial Disorders, methylene blue, treatment

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients with clinically and biopsy confirmed non-neoplasia epithelial disorders of skin and mucosa of vulva.
  • Patient must have a score of 5 or greater in the itching score table before treatment and the itching must last at least 6 months.

Exclusion Criteria:

  • Patients with vulvovaginal or other gynecological trauma, acute inflammatory diseases and other acute illness
  • Patients have been treated with any kind of topical therapy at the vulva within 12 weeks prior to participation in the study
  • Patients with other serious diseases (e.g. liver or kidney diseases) that need immediate treatment
  • Patients with atypical vulvar hyperplasia or vulvar cancer confirmed by biopsy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    treatment group

    Arm Description

    Methylene blue compound injection are mixed by Methylene Blue injection, Dexamethasone powder-injection, Ropivacaine injection and Normal saline injection. Each individual component can help in a very wide range of medical conditions without serious side effects. Every patient received intradermal mixed methylene blue compound injection twice. All patients were observed during the hospitalization at the first injection, and two weeks later they received the second injection at the outpatient department.

    Outcomes

    Primary Outcome Measures

    itching scores
    The patients rate the itching on a visual analogue scale (VAS) before and after the treatment. A VAS is a 100-mm long horizontal line with verbal descriptors at each end to express the extremes of the itching feeling. The most severe itching equals to score 10, and no itching equals to score 0. Patients marked the point on the line that best corresponded to their itching severity.

    Secondary Outcome Measures

    percentage of hypopigmented skin
    Doctors rate the hypopigmented skin on a vulva surface area scale (VSAS) before and after treatment through colposcopy. The vulva area is divided into six regions as labia majora, labia minora, interlabial sulci, clitoris and clitoral hood, perineum, and perianal area. The investigators estimated that the area percentage of labia majora, labia minora, interlabial sulci, clitoris and clitoral hood, perineum, and perianal area was 48%, 24%, 4%, 4%, 10% and 10% differently. Among the six regions, interlabial sulci, clitoris and clitoral hood, perineum, and perianal area could be divided into four equal proportions at most when the area percentage was calculated. And each side of labia majora and labia minora could be divided into four equal proportions at most. If all the vulva area is involved, the VSAS score is 100%, and if no area of vulva is involed, the VSAS score is 0%.

    Full Information

    First Posted
    June 25, 2017
    Last Updated
    November 10, 2022
    Sponsor
    Maternal and Child Health Hospital of Hubei Province
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03200808
    Brief Title
    Methylene Blue Injection for Nonneoplastic Epithelial Disorders of Vulva
    Acronym
    NNEDsMB
    Official Title
    Evaluation of the Efficacy of Mixed Methylene Blue Compound Injection for the Treatment of Nonneoplastic Epithelial Disorders of Vulva.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2022
    Overall Recruitment Status
    Completed
    Study Start Date
    October 1, 2013 (Actual)
    Primary Completion Date
    October 1, 2018 (Actual)
    Study Completion Date
    October 17, 2019 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Maternal and Child Health Hospital of Hubei Province

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The aim of this study is to demonstrate the safety and effectiveness of mixed methylene blue compound Injection for the treatment of nonneoplastic epithelial disorders(NNEDS) of vulva. NNEDS of skin and mucosa of vulva refer to a group of chronic diseases including squamous hyperplasia and lichen sclerosus, which mainly cause vulvar itching and hypopigmentation. Usually the itching is severe may influence social activities and sleep. In addition, NNEDS cause scarring of the vulva which may cause significant sexual dysfunction or pain. The reasons for NNEDs are not clear and the methods of treatment are diverse. The current treatments are primarily local drug (e.g. steroid, calcineurin inhibitors, immunosuppressive agents ), surgical treatments, laser or photodynamic therapy, and the "gold standard" treatment for lichen sclerosus is potent steroids creams. However, all the treatments are not good enough, and the diseases often recur and severely affect women's quality of life. So the investigators reviewed plenty of literatures, and found some authors used single intradermal 1% methylene blue injection for intractable idiopathic pruritus ani and the effect was good. As a preliminary experiment, the investigators used intradermal mixed methylene blue compound injection for a NNEDs patient in the year of 2012, the itching of the patient stopped immediately and the color of the vulva recovered 6 months later. The patient keeps healthy till now. And from then on, the investigators designed this study and to verify the effect and complications of intradermal mixed methylene blue compound injection for the treatment of NNEDS. So far, there is no similar study reported internationally.
    Detailed Description
    Methylene blue compound injection are mixed by Methylene Blue injection, Dexamethasone powder-injection, Ropivacaine injection and Normal saline injection. Each individual component can help in a very wide range of medical conditions without serious side effects. In this study,the investigators used methylene blue compound injection intradermally to treat NNEDs patients. Patients with a diagnosis of biopsy proven NNEDs from Maternal and Child Health Hospital of Hubei Province (China) between October 2013 to October 2016 were recruited. Every patient received intradermal mixed methylene blue compound injection twice. All patients were observed during the hospitalization at the first injection, and two weeks later they received the second injection at the outpatient department. Ages, itching scores, percentage of hypopigmented skin, and recurrences were recorded through inquiry and physical examination before and after treatment. Side effects (such as edema, fever and vulva pain) were also recorded. All women were followed up 1, 3, 6, 12 months after treatment, which included inquiry and physical examination.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Nonneoplastic Epithelial Disorders of Vulva
    Keywords
    Nonneoplastic Epithelial Disorders, methylene blue, treatment

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1
    Interventional Study Model
    Single Group Assignment
    Model Description
    Pations with nonneoplastic epithelial disorders(NNEDS) of vulva.
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    118 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    treatment group
    Arm Type
    Experimental
    Arm Description
    Methylene blue compound injection are mixed by Methylene Blue injection, Dexamethasone powder-injection, Ropivacaine injection and Normal saline injection. Each individual component can help in a very wide range of medical conditions without serious side effects. Every patient received intradermal mixed methylene blue compound injection twice. All patients were observed during the hospitalization at the first injection, and two weeks later they received the second injection at the outpatient department.
    Intervention Type
    Drug
    Intervention Name(s)
    mixed methylene blue compound injection
    Intervention Description
    Every patient received intradermal mixed methylene blue compound injection twice.
    Primary Outcome Measure Information:
    Title
    itching scores
    Description
    The patients rate the itching on a visual analogue scale (VAS) before and after the treatment. A VAS is a 100-mm long horizontal line with verbal descriptors at each end to express the extremes of the itching feeling. The most severe itching equals to score 10, and no itching equals to score 0. Patients marked the point on the line that best corresponded to their itching severity.
    Time Frame
    1 years
    Secondary Outcome Measure Information:
    Title
    percentage of hypopigmented skin
    Description
    Doctors rate the hypopigmented skin on a vulva surface area scale (VSAS) before and after treatment through colposcopy. The vulva area is divided into six regions as labia majora, labia minora, interlabial sulci, clitoris and clitoral hood, perineum, and perianal area. The investigators estimated that the area percentage of labia majora, labia minora, interlabial sulci, clitoris and clitoral hood, perineum, and perianal area was 48%, 24%, 4%, 4%, 10% and 10% differently. Among the six regions, interlabial sulci, clitoris and clitoral hood, perineum, and perianal area could be divided into four equal proportions at most when the area percentage was calculated. And each side of labia majora and labia minora could be divided into four equal proportions at most. If all the vulva area is involved, the VSAS score is 100%, and if no area of vulva is involed, the VSAS score is 0%.
    Time Frame
    1 years
    Other Pre-specified Outcome Measures:
    Title
    pathology changes
    Description
    changes of nonneoplastic epithelial disorders from biopsy pathology
    Time Frame
    1 years

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Patients with clinically and biopsy confirmed non-neoplasia epithelial disorders of skin and mucosa of vulva. Patient must have a score of 5 or greater in the itching score table before treatment and the itching must last at least 6 months. Exclusion Criteria: Patients with vulvovaginal or other gynecological trauma, acute inflammatory diseases and other acute illness Patients have been treated with any kind of topical therapy at the vulva within 12 weeks prior to participation in the study Patients with other serious diseases (e.g. liver or kidney diseases) that need immediate treatment Patients with atypical vulvar hyperplasia or vulvar cancer confirmed by biopsy
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Han Gao, bachelor
    Organizational Affiliation
    Maternal and Child health Hospital of Hubei Province,Wuhan,China
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Xufeng Wu, PH.D
    Organizational Affiliation
    Maternal and Child health Hospital of Hubei Province,Wuhan,China
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Yanli Li, Master
    Organizational Affiliation
    Maternal and Child health Hospital of Hubei Province,Wuhan,China
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    20854400
    Citation
    Neill SM, Lewis FM, Tatnall FM, Cox NH; British Association of Dermatologists. British Association of Dermatologists' guidelines for the management of lichen sclerosus 2010. Br J Dermatol. 2010 Oct;163(4):672-82. doi: 10.1111/j.1365-2133.2010.09997.x. No abstract available.
    Results Reference
    background
    PubMed Identifier
    22669483
    Citation
    Samalavicius NE, Poskus T, Gupta RK, Lunevicius R. Long-term results of single intradermal 1 % methylene blue injection for intractable idiopathic pruritus ani: a prospective study. Tech Coloproctol. 2012 Aug;16(4):295-9. doi: 10.1007/s10151-012-0846-1. Epub 2012 Jun 6.
    Results Reference
    background
    PubMed Identifier
    31628667
    Citation
    Li Y, Shi J, Tan W, Ma Q, Wu X, Gao H. Prospective observational study of the efficacy of mixed methylene blue compound injection for treatment of vulvar non-neoplastic epithelial disorders. Int J Gynaecol Obstet. 2020 Feb;148(2):157-161. doi: 10.1002/ijgo.13007. Epub 2019 Nov 19.
    Results Reference
    derived

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    Methylene Blue Injection for Nonneoplastic Epithelial Disorders of Vulva

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