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
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
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
NCT ID
NCT03200808
First Posted
June 25, 2017
Last Updated
November 10, 2022
Sponsor
Maternal and Child Health Hospital of Hubei Province
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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