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Correlation Pelvic Floor Function and Ultrasound Findings One Year After Childbirth (DeliverUU)

Primary Purpose

Pelvic Floor Disorders, Obstetric Trauma, Urinary Incontinence

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Questionnaire
Pelvic floor ultrasound
Sponsored by
Universitaire Ziekenhuizen KU Leuven
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Pelvic Floor Disorders focused on measuring urinary incontinence, anal incontinence, pelvic organ prolapse, sexual dysfunction, constipation, postpartum, levator avulsion, anal sphincter injury

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • age = or > 18 years
  • Dutch/English-speaking
  • > 33 weeks gestation
  • delivering in UZ Leuven
  • vaginal delivery

Exclusion Criteria:

  • age < 18 years
  • not Dutch/English-speaking
  • < 33 weeks gestation
  • not delivering in UZ Leuven
  • non-vaginal delivery
  • Any disorder, that independently from delivery, affects pelvic floor function or structure, such as, but not limited to musculoskeletal or neurologic diseases.
  • any women with drug addiction, cognitive deficit, language-barrier and illiteracy
  • any disorder or timing or circumstances, which in the Investigator's opinion represents an obstacle to proper informed consent, or safe and/or compliant participation.
  • any prior or simultaneous treatment(s) potentially jeopardising safety or compromising trial integrity.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Participants

    Arm Description

    Outcomes

    Primary Outcome Measures

    Urinary incontinence
    International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-SF) score of ≥1 (score range 0-21, higher scores mean worse urinary incontinence)
    Anal Incontinence
    St Mark's Incontinence Score (SMIS) ≥1 (score range 0-24, higher scores mean worse anal incontinence)
    Sexual dysfunction
    Female Sexual Function Index (FSFI) score ≤ 26.55 (score range 2 to 36, worse scores mean worse sexual function) OR FSDS-R score ≥11 (score range 0 to 52, with higher scores indicating more sexually related distress)
    Constipation according to the Rome IV criteria
    Must include two or more of the following:** Straining during more than ¼ (25%) of defecations Lumpy or hard stools (Bristol Stool Form Scale 1-2) more than ¼ (25%) of defecations Sensation of incomplete evacuation more than ¼ (25%) of defecations Sensation of anorectal obstruction/blockage more than ¼ (25%) of defecations Manual maneuvers to facilitate more than ¼ (25%) of defecations (e.g., digital evacuation, support of the pelvic floor) Fewer than three SBM per week Loose stools are rarely present without the use of laxatives Insufficient criteria for irritable bowel syndrome

    Secondary Outcome Measures

    levator avulsion
    complete avulsion is defined as complete detachment of the puborectalis part of the levator ani muscle from the inferior pubic ramus on 3 out of 8 tomographic ultrasound imaging slices of the pelvic floor during contraction
    levator hiatus antero-posterior diameter (cm)
    levator hiatus latero-lateral diameter (cm)
    levator hiatus surface (cm2)
    anal sphincter injury
    residual defect of at least 30 degrees on Tomographic Ultrasound Imaging
    co-contraction
    approximation of the dorsal puborectalis to the symphysis pubis during Valsalva manoeuvre
    pelvic organ descent
    descent of bladder/cervix/ampulla rectalis under the level of the symphysis pubis
    bladder neck mobility
    axial descent of the bladder neck during Valsalva manoeuvre

    Full Information

    First Posted
    July 6, 2022
    Last Updated
    September 1, 2022
    Sponsor
    Universitaire Ziekenhuizen KU Leuven
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05530681
    Brief Title
    Correlation Pelvic Floor Function and Ultrasound Findings One Year After Childbirth
    Acronym
    DeliverUU
    Official Title
    Correlation Pelvic Floor Function and Ultrasound Findings One Year After Childbirth
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2022 (Anticipated)
    Primary Completion Date
    September 1, 2023 (Anticipated)
    Study Completion Date
    September 1, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Universitaire Ziekenhuizen KU Leuven

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This is a single-center prospective cohort study sponsored by the University Hospitals Leuven (UZ). Women will undergo a pelvic floor ultrasound and will be asked to fill out a questionnaire at the time of their admission into the labour suite, at the postpartum check-up and 12 months postpartum. The primary objective is to correlate self-reported symptoms of Pelvic Floor Dysfunction (PFD) (binary outcome) at one year after delivery with structural changes to the Pelvic Floor Muscles (PFM) and postpartum evidence of levator avulsion (binary indicator) as measured by TransPerineal UltraSound (TPUS). Secondary objectives are to compare demographical and obstetrical variables between patients suffering from PFD symptoms or pelvic floor injury (documented one year after delivery) and those who do not; to record how patients manage and cope with PFD including recovery and compliance with Pelvic Floor Muscle Training (PFMT) as prescribed in the standard pathway of peripartum care; and to use of TPUS images for the development of artificial intelligence tools for automated image analysis. Primary outcomes are PFD symptoms one year after delivery and injury to the PFM evidenced by POP-Q and TPUS. The demographic variables and information about the pregnancy and the delivery will be obtained from the medical records. The presence and severity of PFD will be measured using standardized self-reporting tools: Pelvic Organ Prolapse Distress Index (POP-DI), Patient Assessment Constipation-SYMptoms (PAC-SYM), International Consultation on Incontinence Questionnaire - Urinary Incontinence - Short Form (ICIQ-SF), St. Mark's Incontinence Score (SMIS), Female Sexual Function Index (FSFI), Female Sexual Distress Scale - Revised (FSDS-R). FSFI is a widely used generic tool with sufficient granularity and validated in a large number of languages. FSDS-R assesses the construct "personal distress", which has been considered as an additional important aspect contributing to sexual dysfunction of women. PFD, as a clustered outcome, being the presence of any kind of pelvic floor dysfunction symptoms, will be defined as POP-DI score of ≥11 OR ICIQ-SF score of ≥1 OR SMIS score of ≥1 OR FSFI score ≤ 26.55 OR FSDS-R score ≥11.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Pelvic Floor Disorders, Obstetric Trauma, Urinary Incontinence, Anal Incontinence, Pelvic Organ Prolapse, Pelvic Pain, Sexual Dysfunction, Constipation, Anal Sphincter Injury
    Keywords
    urinary incontinence, anal incontinence, pelvic organ prolapse, sexual dysfunction, constipation, postpartum, levator avulsion, anal sphincter injury

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    320 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Participants
    Arm Type
    Experimental
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    Questionnaire
    Intervention Description
    The survey consists in standardized and validated questionnaires on urinary function (ICIQ-SF, 4 items), bowel function (SMIS, 7 items and PAC-SYM, 12 items), symptoms of prolapse (POPDI, 6 items) and sexual function (Female Sexual Function Index FSFI, 19 items and Female Sexual Distress Scale - Revised FSDS-R, 13 items). questionnaire will be used at recruitment, at the postpartum visit, at the first annual follow-up visit.
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    Pelvic floor ultrasound
    Other Intervention Name(s)
    Transperineal ultrasound, Pelvic floor sonography
    Intervention Description
    Pelvic floor ultrasound is the preferred imaging modality for documenting pelvic floor anatomy during pregnancy or after delivery. This examination is routinely performed in the outpatient clinic during patient visits (including the one year check-up after delivery). The technique used to assess the pelvic floor is described in detail in the 2019 practice parameters issued by IUGA.
    Primary Outcome Measure Information:
    Title
    Urinary incontinence
    Description
    International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-SF) score of ≥1 (score range 0-21, higher scores mean worse urinary incontinence)
    Time Frame
    one year postpartum
    Title
    Anal Incontinence
    Description
    St Mark's Incontinence Score (SMIS) ≥1 (score range 0-24, higher scores mean worse anal incontinence)
    Time Frame
    one year postpartum
    Title
    Sexual dysfunction
    Description
    Female Sexual Function Index (FSFI) score ≤ 26.55 (score range 2 to 36, worse scores mean worse sexual function) OR FSDS-R score ≥11 (score range 0 to 52, with higher scores indicating more sexually related distress)
    Time Frame
    one year postpartum
    Title
    Constipation according to the Rome IV criteria
    Description
    Must include two or more of the following:** Straining during more than ¼ (25%) of defecations Lumpy or hard stools (Bristol Stool Form Scale 1-2) more than ¼ (25%) of defecations Sensation of incomplete evacuation more than ¼ (25%) of defecations Sensation of anorectal obstruction/blockage more than ¼ (25%) of defecations Manual maneuvers to facilitate more than ¼ (25%) of defecations (e.g., digital evacuation, support of the pelvic floor) Fewer than three SBM per week Loose stools are rarely present without the use of laxatives Insufficient criteria for irritable bowel syndrome
    Time Frame
    one year postpartum
    Secondary Outcome Measure Information:
    Title
    levator avulsion
    Description
    complete avulsion is defined as complete detachment of the puborectalis part of the levator ani muscle from the inferior pubic ramus on 3 out of 8 tomographic ultrasound imaging slices of the pelvic floor during contraction
    Time Frame
    1 year
    Title
    levator hiatus antero-posterior diameter (cm)
    Time Frame
    1 year
    Title
    levator hiatus latero-lateral diameter (cm)
    Time Frame
    1 year
    Title
    levator hiatus surface (cm2)
    Time Frame
    1 year
    Title
    anal sphincter injury
    Description
    residual defect of at least 30 degrees on Tomographic Ultrasound Imaging
    Time Frame
    1 year
    Title
    co-contraction
    Description
    approximation of the dorsal puborectalis to the symphysis pubis during Valsalva manoeuvre
    Time Frame
    1 year
    Title
    pelvic organ descent
    Description
    descent of bladder/cervix/ampulla rectalis under the level of the symphysis pubis
    Time Frame
    1 year
    Title
    bladder neck mobility
    Description
    axial descent of the bladder neck during Valsalva manoeuvre
    Time Frame
    1 year

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    45 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: age = or > 18 years Dutch/English-speaking > 33 weeks gestation delivering in UZ Leuven vaginal delivery Exclusion Criteria: age < 18 years not Dutch/English-speaking < 33 weeks gestation not delivering in UZ Leuven non-vaginal delivery Any disorder, that independently from delivery, affects pelvic floor function or structure, such as, but not limited to musculoskeletal or neurologic diseases. any women with drug addiction, cognitive deficit, language-barrier and illiteracy any disorder or timing or circumstances, which in the Investigator's opinion represents an obstacle to proper informed consent, or safe and/or compliant participation. any prior or simultaneous treatment(s) potentially jeopardising safety or compromising trial integrity.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jan Deprest, MD, PhD
    Phone
    +3216344269
    Email
    jan.deprest@uzleuven.be
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jan Deprest, MD, PhD
    Organizational Affiliation
    Universitaire Ziekenhuizen KU Leuven
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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    Correlation Pelvic Floor Function and Ultrasound Findings One Year After Childbirth

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