Vaginal Axis on Magnetic Resonance Imaging After Laparoscopic Pectopexy Surgery: a Controlled Study
NCT ID: NCT05876975
Last Updated: 2023-05-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
21 participants
INTERVENTIONAL
2023-01-04
2023-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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procedure: laparoscopic pectopexy
MRI evaluation will be conducted on eleven participants who underwent laparoscopic pectopexy surgery after one month.
laparoscopic pectopexy
Women with pelvic organ prolapse and suitable indications underwent laparoscopic pectopexy.
Nulliparous women with no uterovaginal prolapsed
Ten nulliparous participants with no uterovaginal prolapsed will be evaluate by MRI
No interventions assigned to this group
Interventions
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laparoscopic pectopexy
Women with pelvic organ prolapse and suitable indications underwent laparoscopic pectopexy.
Eligibility Criteria
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Inclusion Criteria
* Nulliparous women without pelvic organ prolapse (asymptomatic grade 1 or less) who presented to the outpatient clinic with complaints other than POP symptoms (e.g., menstrual irregularity) were randomly selected and assigned as the control group.
Exclusion Criteria
* Women with any congenital or acquired anatomical or reproductive anomaly.
* Women diagnosed with enterocele through transperineal ultrasound prior to enrollment.
* Women who require hysterectomy or concomitant pelvic organ prolapse (POP) or anti- incontinence procedure.
* Women with abnormal uterine bleeding.
* Women with abnormal cervical screening test results.
In Control Group
* Women who have given birth previously.
* Women with a history of pelvic organ prolapse or any pelvic floor disorders.
* Women who have undergone pelvic surgery.
* Women with any congenital or acquired anatomical or reproductive anomaly.
* Women with abnormal uterine bleeding.
* Women with abnormal cervical screening test results.
18 Years
80 Years
FEMALE
Yes
Sponsors
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Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
OTHER
Responsible Party
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fatih sahin
MD / Principal Investigator
Principal Investigators
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fatih şahin, MD
Role: PRINCIPAL_INVESTIGATOR
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Locations
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Prof. Dr. Cemil Taşcıoğlu City Hospital
Istanbul, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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References
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Wang H, Shen J, Li S, Gao Z, Ke K, Gu P. The feasibility of uterine-vaginal axis MRI-based as evaluation of surgical efficacy in women with pelvic organ prolapse. Ann Transl Med. 2022 Apr;10(8):447. doi: 10.21037/atm-22-1173.
Other Identifiers
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77
Identifier Type: -
Identifier Source: org_study_id
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