Clinical trials: Pelvic Prolapse
Prolapse
Affixing Polypropylene Mesh Using Barbed Suture (Quill™ Srs) During Laparoscopic Sacrocolpopexy Randomized Controlled Trial (Quill Lsc)
1.0 STUDY OBJECTIVE 1.1 PRIMARY OBJECTIVE - To compare two methods of polypropylene mesh attachment during laparoscopic sacrocolpopexy (LSC): running technique using self-anchoring 1 barbed delayed absorbable suture (Quill™ SRS…
- Trial name
- QUILL-LSC (NCT01551992)
- Testing
- Quill suture vs. Interrupted suture
- Where
- United States
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- Kaiser Permanente
Overactive Bladder
Assessment of Potential Biomarkers in Women With Symptoms of Overactive Bladder and Pelvic Organ Prolapse
The objective of this study is to investigate the role of certain biomarkers in the initial assessment of women with overactive bladder (OAB).
- Trial name
- NCT03516292
- Testing
- Urinary Nerve Growth Factor
- Where
- Greece
- Volunteers
- 108 people
- Sponsor
- Aristotle University Of Thessaloniki
Rectal Prolapse
Breakthrough Improvement Collaborative for Ventral Mesh Rectopexy
Different studies showed large variation between care processes in multiple diseases, this leads to large variation in outcomes.
- Trial name
- BIC4VMR (NCT05728554)
- Testing
- Learning session 1, Learning session 2, Learning session 3
- Where
- Belgium
- Volunteers
- 320 people
- Sponsor
- KU Leuven
Pelvic Organ Prolapse
Safety and Performance of the EndoFast Reliant SCP in Vaginal Wall Reinforcement
A Single arm, single site, retrospective cohort Post Marketing Clinical Follow up Study Evaluating the Safety and Performance of the EndoFast Reliant SCP for apical support.
- Trial name
- NCT03516136
- Testing
- EndoFast Reliant SCP
- Volunteers
- 84 people
- Sponsor
- Allium, Ltd.
Female Urogenital Diseases, Urinary Incontinence
Clinical Trial of "Magic Gyno" Laser Device
The aim of this prospective study is investigation of efficiency and safety of medical device "Magic Gyno" in accordance with the stated purpose.
- Conditions
- Female Urogenital Diseases, Urinary Incontinence, Prolapse Genital, Menopausal Syndrome
- Trial name
- NCT05463081
- Testing
- Laser treatment, Blood test, Clinical urine test
- Where
- Russia
- Volunteers
- 70 people
- Sponsor
- MeLSyTech, Ltd
Stress Urinary Incontinence, Pelvic Organ Prolapse
Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry
The objective of this post market, clinical registry is to evaluate the performance of the products of the TVT family of products or vaginal vault or uterine prolapse repair (with laparotomic or laparoscopic approach including…
- Trial name
- NCT04829175
- Testing
- Intervention
- Where
- 10 sites in United States, Austria and 5 more
- Volunteers
- 1,000 people
- Sponsor
- Ethicon, Inc.
Vaginal Vault Prolapse
Laparoscopic Sacropexy: Comparison of Mesh Attachment
The purpose of this study is to compare postoperative complications and outcome two different attachment sites of the dorsal mesh support in laparoscopic sacropexy.
- Trial name
- MeshPlace (NCT00928239)
- Testing
- laparoscopic sacropexy with mid vaginal attachment, laparoscopic sacropexy with caudal vaginal attachment
- Where
- Switzerland
- Volunteers
- 88 people, healthy volunteers welcome
- Sponsor
- Kantonsspital Aarau
Cystocele
Changes of Pad Weight Results and Urethral Pressure Profiles After Reduction of Cystocele by Vaginal Gauze Packing
The purpose of this study is to retrospectively review the impact of vaginal packing on the urodynamic studies, especially for urethral pressure profiles.
- Trial name
- NCT01559558
- Testing
- vaginal packing
- Where
- Taiwan
- Volunteers
- 140 people
- Sponsor
- National Taiwan University Hospital
Pelvic Organ Prolapse
Gabapentin for Postop Pain After SSLF
Purpose: To assess the impact of gabapentin versus placebo on overall postoperative pain and gluteal pain at 7 days after vaginal sacrospinous ligament suspension for apical pelvic organ prolapse.
- Trial name
- NCT03123861
- Testing
- Gabapentin
- Where
- United States
- Volunteers
- 45 people
- Sponsor
- University of North Carolina, Chapel Hill
Pelvic Floor Dysfunction, Postpartum Care
Comparison of Outpatient Rehabilitation Versus Self-training for the Treatment and Prevention of Postpartum Pelvic Floor Dysfunction
The main goal of this study to compare self-training postpartum and training with a specialist support (physiotherapist and physical medicine and rehabilitation doctor) effect on pelvic floor dysfunction prevention and treatment…
- Conditions
- Pelvic Floor Dysfunction, Postpartum Care, Postpartum Comfort, Female Urinary Incontinence and Pelvic Organ Prolapse
- Trial name
- DDDPREV (NCT07426770)
- Testing
- Rehabilitation postpartum, Self-training
- Where
- Lithuania
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Vilnius University
Rectal Prolapse, Pelvic Organ Prolapse (POP)
RECTOSACROUTEROPEXY vs. WELLS
The goal of this clinical trial was to compare two surgical techniques in female patients with full-thickness rectal prolapse. The main questions it aimed to answer were: 1.
- Trial name
- RSUP (NCT07673406)
- Testing
- Modified rectosacrouteropexy, Wells rectopexy
- Where
- Azerbaijan
- Volunteers
- 36 people
- Sponsor
- Azerbaijan Medical University
Pelvic Floor Prolapse
Prolift Versus IVS for Pelvic Floor Prolapse
Women who underwent mesh or sling procedures to correct pelvic organ prolapse will be enrolled. Their data will be collected from the files.
- Trial name
- NCT01383291
- Where
- 2 sites in Israel
- Sponsor
- Western Galilee Hospital-Nahariya
Pelvic Organ Prolapse
Enabling Self-Care for Pessary Users in Rural Setting
This study is to see if a using new collapsible pessary (Reia pessary) for treatment of pelvic organ prolapse will allow patients to care for their prolapse on their own, rather than having to come to be seen by a provider in the…
- Trial name
- ESCAPE (NCT07084818)
- Testing
- Reia System pessary self-care management, Standard pessary office-based management
- Where
- United States
- Volunteers
- 120 people
- Sponsor
- Dartmouth-Hitchcock Medical Center
Pelvic Organ Prolapse
Preoperative Analgesia by Infiltration of the Pudendal Nerve Prior to Sacrospinous Ligament Suspension
Pelvic organ prolapse is a common problem. It affects about half of women and causes uncomfortable bulge sensations (similar to sitting on a ball), urine and stool problems, difficulty with sexual activity and embarrassment.
- Trial name
- PAINS (NCT04733560)
- Testing
- Pudendal nerve block, Bupivacaine Injectable Product
- Where
- Canada
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Fraser Health
Pelvic Organ Prolapse
Vaginal Tactile Imaging for the Assessment of Pelvic Organ Prolapse Repair Efficiency
Female patients with POP will be evaluated for vaginal elasticity using vaginal tactile imaging both before and after surgery for the repair of the POP.
- Trial name
- NCT03311685
- Testing
- vaginal tactile imager
- Where
- Israel
- Volunteers
- 30 people
- Sponsor
- Rambam Health Care Campus
Lower Urinary Tract Symptom in Severe Cystocele Women
Prevalence Rates of USI, BO, DO and Their Clinical and Urodynamic Findings in Women With ≥Stage II Cystocele
Prevalence rates of urodynamic stress incontinence (USI), bladder oversensitivity (BO) /detrusor overactivity (DO) or both and their related clinical and urodynamic findings in women with ≥ pelvic organ prolapse quantification…
- Trial name
- NCT03613350
- Testing
- Pad test
- Volunteers
- 480 people
- Sponsor
- National Taiwan University Hospital
Vaginal Vault Prolapse
Traditional Vaginal Surgery VS Autologous Tissue in Pelvic Floor Repair
The goal of this randomized, non blind, one center study is to compare the efficacy of vNOTES (vaginal natural orifice transluminal surgery) and traditional vaginal operation between the two groups by determining the risk of…
- Trial name
- PREFAP (NCT05628831)
- Testing
- vNOTES suspension with autologous tissue, Vaginal surgery
- Where
- Croatia
- Volunteers
- 56 people
- Sponsor
- General Hospital Zadar
Pelvic Organ Prolapse
Assessment of Quality of Life in Disorders of the Pelvic Floor
The purpose of this study is to compare the touch-screen version of the PFDI-20, PFIQ-7, PISQ 12 and SF-36 french questionnaires to their paper versions.
- Trial name
- U-GYN-QOL (NCT01134588)
- Testing
- Paper questionnaire, Touch screen questionnaire
- Where
- France
- Volunteers
- 129 people
- Sponsor
- Centre Hospitalier Universitaire de Nīmes
Bladder Oversensitivity, Detrusor, Overactive
BO and DO in Women With Cystocele Before and After Cystocele Repair
The changes of lower urinary tract function after cystocele repair are important for perioperative consultation and management. Thus, the aim of this retrospective study was to evaluate the prevalence of bladder oversensitivity…
- Trial name
- NCT04981054
- Testing
- Cystocele repair
- Where
- Taiwan
- Volunteers
- 483 people
- Sponsor
- National Taiwan University Hospital
Infertility, Female, Pelvic Organ Prolapse
Apical Pelvic Support in Infertility Patients
This study aims to evaluate apical pelvic compartment support in infertility patients at the time of hysteroscopy. Apical pelvic compartment evaluation for pelvic organ prolapse will be performed in infertility patients…
- Conditions
- Infertility, Female, Pelvic Organ Prolapse, Pelvic Floor Disorders
- Trial name
- NCT04039009
- Testing
- Pelvic Organ Prolapse Quantification system
- Where
- Turkey (Türkiye)
- Volunteers
- 1,100 people
- Sponsor
- Uludag University