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Trial registered on ANZCTR
Registration number
ACTRN12614000904673
Ethics application status
Approved
Date submitted
26/07/2014
Date registered
25/08/2014
Date last updated
25/02/2022
Date data sharing statement initially provided
25/02/2022
Type of registration
Retrospectively registered
Titles & IDs
Public title
Effects of pregnancy and childbirth on pelvic floor morphology and sexual function in Egyptian women
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Scientific title
Evaluation of levator ani muscle integrity in early postpartum period using three dimensional pelvic floor translabial ultrasound, in women after vaginal versus elective or urgent cesarean section, and study of its effects on sexual function in Egyptian women.
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Secondary ID [1]
285042
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Nil Known
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Universal Trial Number (UTN)
U1111-1159-6256
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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:
screening for postpartum female pelvic floor muscle "levator ani" affection.
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screening for postpartum sexual function in Egyptian women.
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Condition category
Condition code
Reproductive Health and Childbirth
292869
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0
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Childbirth and postnatal care
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
1- transperineal pelvic floor ultrasound applied for the submitted 120 women "primiparae" (40 women after normal vaginal delivery), (40 women after urgent cesarean section), (40 women after elective cesarean section), in early postpartum period (48 to 72) hours postpartum, to evaluate levator ani morphology, according to Edessy Pelvic floor Integrity Score (EPIS), This is a unique scoring system based on trans-perineal ultrasonographic evaluation of levator ani muscle morphology and biometric measures. This scoring system has 4 items (levator hiatus area LHA), (levator ani avulsion side), (levato urethral gap LUG), and (levator ani avulsion size), Score from 0 to= 3 considered severely malfunctioning female pelvic floor. Score from 4 to= 6 considered mildly malfunctioning female pelvic floor. Score > 6 up to 8 considered well-functioning female pelvic floor.
2- answering of the validated female sexual function index (F.S.F.I) three months postpartum period for same cases submitted to ultrasound.
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Intervention code [1]
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Not applicable
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Comparator / control treatment
transperineal pelvic floor ultrasound applied for the 40 women after elective cesarean section in early postpartum period (48 to 72) hours postpartum, to evaluate levator ani morphology.
and answering of the validated female sexual function index (F.S.F.I) three months postpartum period for same cases submitted to ultrasound.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Pelvic floor muscle strength as assessed by three/four dimensional translabial pelvic floor ultrasound
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Assessment method [1]
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Timepoint [1]
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early postpartum period (48 to 72) hours postpartum
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Primary outcome [2]
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Sexual function of pelvic floor as assessed by the validated female sexual function index
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Assessment method [2]
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Timepoint [2]
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at 3 months after delivery
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Secondary outcome [1]
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Trauma or avulsion of levator ani muscle as assessed by three/four dimensional translabial pelvic floor ultrasound
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Assessment method [1]
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Timepoint [1]
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6 months after delivery.
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Secondary outcome [2]
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Sexual function as assessed by the validated female sexual function index
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Assessment method [2]
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Timepoint [2]
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3 months after delivery
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Eligibility
Key inclusion criteria
primiparae in early postpartum period (48 hours to72 hours).
written consent was taken.
easy communicable, reachable women for further requirements.
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Minimum age
No limit
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. Refused consent.
2. Previous vaginal or cesarean delivery.
3. Severe mental illness.
4. Severe physical handicap or difficulties in communication.
5. Women without postpartum active sexual life or separate from their spouse.
6. Past history of sexual dysfunction.
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Study design
Purpose
Screening
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Duration
Longitudinal
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Selection
Defined population
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Timing
Both
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
12/03/2013
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Actual
29/05/2013
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Date of last participant enrolment
Anticipated
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Actual
10/02/2014
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Date of last data collection
Anticipated
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Actual
17/12/2014
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Sample size
Target
120
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Accrual to date
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Final
120
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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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Alexandria
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Al-azhar university.
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Address [1]
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1 Al-mokhayam aldaem street, Nasr city, Cairo (PO:11471)
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Country [1]
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Egypt
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Primary sponsor type
University
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Name
Alazhar university
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Address
1 Al-mokhayam aldaem street, Nasr city, Cairo (PO:11823)
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Country
Egypt
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Secondary sponsor category [1]
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Hospital
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Name [1]
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Al-azhar university Hospital
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Address [1]
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1 Gawhar Al-kaed street, Darasah, Cairo (PO:11633)
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Country [1]
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Egypt
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Alazhar university ethics committee
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Ethics committee address [1]
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1 Al-mokhayam aldaem street, Nasr city, Cairo (PO:11471)
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Ethics committee country [1]
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Egypt
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Date submitted for ethics approval [1]
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Approval date [1]
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15/02/2013
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Ethics approval number [1]
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Summary
Brief summary
To evaluate levator ani morphology following normal vaginal delivery and cesarean section (elective and emergent), using three-dimensional (3D) ultrasound, and to study the effect of mode of delivery on female sexual function.
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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 MUHAMED OSMAN MUHAMED MUHAMED
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Address
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SAUDI ARABIA, ALBAHA, KING FAHAD HOSPITAL ,
ALAZHAR STREET,
ZIP CODE: 65732
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Country
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Saudi Arabia
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Phone
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+966551321266
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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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MUHAMED OSMAN
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Address
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SAUDI ARABIA, ALBAHA, KING FAHAD HOSPITAL ,
ALAZHAR STREET,
ZIP CODE: 65732
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Country
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Saudi Arabia
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Phone
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+966551321266
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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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Mahmoud sayed el-edessy
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Address
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Professor at Al-azhar university, 52 mohey el deen abo el-ez street, mohandsein, Giza (Post code:12655)
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Country
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Egypt
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Phone
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+201005646785
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Fax
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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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
No additional documents have been identified.
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