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Trial registered on ANZCTR
Registration number
ACTRN12617000524392
Ethics application status
Not required
Date submitted
16/12/2016
Date registered
10/04/2017
Date last updated
10/04/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
Platelet-rich plasma (PRP) local injection for female sexual dysfunction
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Scientific title
Platelet- rich plasma (PRP) local injection for female sexual dysfunction
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Secondary ID [1]
290779
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none
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Universal Trial Number (UTN)
U1111-1191-0080
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Sexual dysfunction
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Condition category
Condition code
Reproductive Health and Childbirth
301133
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0
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Other reproductive health and childbirth disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
A small sample of blood (5ml) is withdrawn from the patient, then spun in a centrifuge to separate the blood into layers. The platelet-rich plasma layer is carefully extracted, then injected back into the anterior and posterior vaginal wall, G-spot and clitoris. the procedure will take about 10 minutes after local anaesthetic cream application.procedure will be done in the outpatient clinic by gynaecology specialist with minimum 3 years experience.patients will receive four times injections 2weeks a part.they will be evaluated by FSFI questionnaire after 2 months.
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Intervention code [1]
296690
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Treatment: Other
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Comparator / control treatment
No control group' in this field
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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change in sexual function accessed by FSFIq before and after the procedure.
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Assessment method [1]
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Timepoint [1]
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2 months after PRP injection
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Secondary outcome [1]
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1-The incidence of vaginal infection assessed by self-report.
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Assessment method [1]
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Timepoint [1]
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2 months after PRP injection.
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Secondary outcome [2]
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2-change in urinary incontinence in patients complaining of incontinence.
will be assessed by ICIQ short form questionnaire.
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Assessment method [2]
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Timepoint [2]
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2 months after PRP injection
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Eligibility
Key inclusion criteria
sexually active females 18-60 years complaining of sexual dysfunction.
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Minimum age
18
Years
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Maximum age
60
Years
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Sex
Females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
1- psychological or mental illness.
2- male partner erectile dysfunction.
3- diabetic patients
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
pilot study
Statistical presentation and analysis of the study will be conducted using mean, standard deviation and chi-square test .
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
20/04/2017
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Actual
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Date of last participant enrolment
Anticipated
20/08/2017
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Actual
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Date of last data collection
Anticipated
30/10/2017
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Actual
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Sample size
Target
40
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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Egypt
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State/province [1]
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cairo
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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AL ZAHRAA UNIVERSITY HOSPITAL
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Address [1]
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AL ZAHRAA UNIVERISITY HOSPITAL
CAIRO
ABASSIA
AZHAR UNIVERSITY
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Country [1]
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Egypt
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Primary sponsor type
Individual
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Name
DOAA MOHAMED SALEH
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Address
ALZAHRAA UNIVEISITY HOSPITSL
ABASSIA
CAIRO
EGYPT
AZHAR UNIVERSITY
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Country
Egypt
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Secondary sponsor category [1]
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Individual
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Name [1]
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TAISEER MAROUF
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Address [1]
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PROFESSOR OB/GYN
AL ZAHRAA UNIVEROSITY HOSPITAL
ABASSIA
CAIRO
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Country [1]
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Egypt
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Ethics approval
Ethics application status
Not required
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Summary
Brief summary
Platelet Rich Plasma (PRP) has been demonstrated to be effective and without serious side effects in multiple studies in the areas of wound care, orthopaedics, dental surgery and in a variety of cosmetic procedures. PRP activates pluripotent stem cells in the area of injection resulting in rejuvenation and even enhancement of damaged or undamaged tissue. The aqueous nature of PRP allows injection through a small bore needle and an even distribution throughout the tissue surrounding the injection site. women who presented with complaints of dyspareunia or other symptoms related to sexual dysfunction will be offered PRP injections into the periurethral area of the Skene's glands, vaginal wall and the clitoris and will be observed for their responses to this treatment. It will offer a cheap, easy, non-invasive and safe treatment for females with sexual dysfunction.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr doaa mohamed saleh
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Address
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AL ZAHRAA UNIVERISITY HOSPITAL,AZHAR UNIVERISITY
ABASSIA
,Cairo
,EGYPT
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Country
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Egypt
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Phone
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+201096565703
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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taiseer marouf
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Address
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PROFESSOR OB/GYN
AZHAR UNIVERSITY
AL ZAHRA UNIVERISITY HOSPITAL
,CAIRO
,EGYPT
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Country
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Egypt
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Phone
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+201223660078
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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nahed ezzat
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Address
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assistantprofessor OB/GYN
AZHAR UNIVERSITY
AL ZAHRA UNIVERISITY HOSPITAL
CAIRO
,EGYPT
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Country
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Egypt
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Phone
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+20122654789
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Clinical evaluation of autologous platelet rich plasma injection in postmenopausal vulvovaginal atrophy: A pilot study.
2022
https://dx.doi.org/10.1111/jocd.14873
N.B. These documents automatically identified may not have been verified by the study sponsor.
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