Clinical trials: Pelvic Prolapse
Female Stress Incontinence, Pelvic Organ Prolapse
Collection of Long Term Patient Outcomes Data Following Implantation of AMS Surgical Devices
To monitor post-market performance through evaluation of short and long-term performance via: Efficacy Safety Patient reported outcomes
- Trial name
- CAPTURE (NCT01673360)
- Testing
- Elevate PC, Mini Arc Pro, RetroArc
- Where
- 19 sites in United States, Canada and 6 more
- Volunteers
- 401 people
- Sponsor
- ASTORA Women's Health
Unrecognized Condition
Different Surgical Techniques Used for Prolapse Repair in Elderly Patient
The investigator aimed to compare various pelvic floor repairs in female aged from 70 to 80 years old, to see which procedure in terms of treatment-related complications of SCP, VMR and NTR by comparing the operative and…
- Trial name
- NCT03445442
- Testing
- SCP, NTR, VMR
- Volunteers
- 214 people
- Sponsor
- Centre Hospitalier Universitaire de Nice
Degree of Uterine Prolapse and Its Effect on Quality of Life
Quality of Life Assessment in Patients With Different Degrees of Pelvic Organ Prolapse
Study design: The study building by two design a descriptive exploratory research design and quasi experimental research design were utilized in the present study Setting of the study: This study was conducted at the Outpatient…
- Trial name
- NCT07080203
- Where
- Egypt
- Volunteers
- 400 people, healthy volunteers welcome
- Sponsor
- Sohag University
Colo-rectal Cancer, Rectal Prolapse
Evaluation of SINGLE PORT (SP) Robotic Technology in Colorectal Surgery
Currently a multiport robotic surgery platform (Intuitive Xi) is widely available and used for colorectal surgery indications. A Single port platform (Intuitive SP) is FDA approved for Head and Neck and Urology but has not been…
- Conditions
- Colo-rectal Cancer, Rectal Prolapse, Colostomy Stoma, Colorectal Disorders
- Trial name
- NCT05321134
- Testing
- Single port robotic colorectal surgical procedure
- Where
- United States
- Volunteers
- 25 people
- Sponsor
- University of California, Davis
Pelvic Organ Prolapse
Laparoscopic Retrovesical Colpopectinopexia
The purpose of this study is to identify whether a new operative technic would be acceptable in female with pelvic organ prolapse.
- Trial name
- prolapse (NCT02919852)
- Testing
- laparoscopic retrovesical colpopectinopexia
- Where
- Ukraine
- Volunteers
- 70 people
- Sponsor
- Orel Regional Hospital, Russia
Internal Hemorrhoid, Rectal Prolapse
CAES for Internal Hemorrhoids and Rectal Prolapse
Cap-assisted endoscopic sclerotherapy (CAES) is a new interventional therapy for internal hemorrhoids and rectal prolapse under colonoscopy.
- Trial name
- NCT04169152
- Testing
- Cap-assisted endoscopic sclerotherapy
- Where
- China
- Volunteers
- 10,000 people
- Sponsor
- Faming Zhang
Rectal Prolapse
Laparoscopic Suture Versus Mesh Rectopexy for the Treatment of Persistent Complete Rectal Prolapse in Children
Purpose: to compare Laparoscopic mesh rectopexy with laparoscopic suture rectopexy The operative time, recurrence rate, post-operative constipation, and effect on fecal incontinence, were reported and evaluated for each group…
- Trial name
- NCT04117633
- Testing
- Laparoscopy
- Volunteers
- 64 people
- Sponsor
- Al-Azhar University
Modified Extraperitoneal Uterosacral Ligament Suspension, Vault Prolapse, Vaginal
Modified Uterosacral Ligament Suspension in Vaginal Hysterectomy
Introduction : The extraperitoneal uterosacral ligament suspension (ULS) can be performed during the removal of the uterus in vaginal hysterectomy to prevent cuff prolapse.
- Trial name
- NCT03832543
- Volunteers
- 40 people
- Sponsor
- Kanuni Sultan Suleyman Training and Research Hospital
Pelvic Organ Prolapse
The Purpose of This Study is to Look at Pelvic Support Problems, Also Commonly Known as Pelvic Organ Prolapse
FemmeJock is a pelvic floor support system developed by pelvic floor physiotherapists for patients with pelvic organ prolapse in order to ameliorate symptoms of pelvic floor pressure and discomfort.
- Trial name
- NCT00964197
- Testing
- FemmeJock
- Where
- United States
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- University of Oklahoma
Vaginal Vault Prolapse
Laparoscopic Sacrocolpopexy: Long Term Follow-up
The purpose of this study is to determine the long term results of laparoscopic sacrocolpopexy regarding anatomical results, recurrences, complications, further surgeries required, patients satisfaction and quality of life.
- Trial name
- NCT01394237
- Testing
- Examination
- Where
- Switzerland
- Volunteers
- 75 people
- Sponsor
- Kantonsspital Aarau
Cystocele
Transvaginal Versus Transobturator Paravaginal Repair
Clinical trial comparing the new technique for paravaginal repair versus the traditional technique
- Trial name
- NCT03489902
- Testing
- Transobturator Paravaginal Repair, traditional transvaginal Paravaginal Repair
- Volunteers
- 40 people
- Sponsor
- Ain Shams Maternity Hospital
Pelvic Organ Prolapse
Pectopexy Surgery Without Mesh
it is aimed to examine the effect of laparoscopic pectopexy surgery without mesh on Pelvic Organ Prolapse Measurement (POP-Q) and quality of life of the patient.
- Trial name
- NCT05715489
- Testing
- Comparison of pre and postoperative POP-Q values of the patients, Comparison of pre and postoperative PISQ-12 scores of the patients
- Where
- Turkey (Türkiye)
- Volunteers
- 38 people, healthy volunteers welcome
- Sponsor
- Gaziosmanpasa Research and Education Hospital
Pelvic Floor Disorders, Pelvic Pain
Digital Care Programs for Female Pelvic Health
The purpose of this study is to create a research repository, composed of data collected in the course of digital care programs for pelvic health conditions by SWORD Health/Bloom to individuals undergoing those programs.
- Conditions
- Pelvic Floor Disorders, Pelvic Pain, Pelvic Organ Prolapse, Pelvic Floor Muscle Weakness
- Trial name
- NCT05513417
- Testing
- Bloom Pod
- Where
- United States
- Volunteers
- 50,000 people, healthy volunteers welcome
- Sponsor
- Sword Health, SA
Pelvic Organ Prolapse, Prolapse
A New POP (Pelvic Organ Prolapse) Scoring System: Validity and Reliability
There is a strong need for a better, simplified and informative applicable classification system that should be used to speak a common descriptive language among health care providers that treat POP.
- Conditions
- Pelvic Organ Prolapse, Prolapse, Prolapse, Vaginal, Prolapse Uterus
- Trial name
- NCT06520722
- Testing
- Prolapse scoring system
- Where
- Egypt
- Volunteers
- 75 people
- Sponsor
- Cairo University
Pelvic Organ Prolapse, Stress Urinary Incontinence
What is the Effect of Prolapse Surgery on Voiding?
The aim of our study is to examine the effect of prolapse surgery on voiding. Our study is the very first one to combine several innovative low-invasive and low-cost methods to analyse the amelioration or deterioration of voiding…
- Conditions
- Pelvic Organ Prolapse, Stress Urinary Incontinence, Overactive Bladder, Voiding Disorders
- Trial name
- PROVOID (NCT04429360)
- Testing
- pelvic reconstructive surgery
- Where
- Belgium
- Volunteers
- 453 people
- Sponsor
- Universiteit Antwerpen
Cystocele
Trial Comparing Laparoscopic Sacropexy and Vaginal Mesh Surgery for Women Cystocele Repair.
The primary objective of this study is to compare with PFDI-20 questionnaire the functional outcome of laparoscopic sacrocolpopexy and vaginal mesh surgery in the treatment of symptomatic exteriorised cystocele up to 4 years…
- Trial name
- PROSPERE4 (NCT02272361)
- Testing
- laparoscopic sacrocolpopexy, vaginal mesh surgery
- Where
- 12 sites in France
- Volunteers
- 220 people
- Sponsor
- University Hospital, Lille
Stress Urinary Incontinence, Urge Incontinence
Enhanced Consent and Preparedness for Surgery Trial
To develop an audiovisual decision aid (AVDA) to improve the informed consent process. The investigators aim to examine the impact of a comprehensible AVDA that is written below the 8th grade reading level.
- Conditions
- Stress Urinary Incontinence, Urge Incontinence, Pelvic Organ Prolapse
- Trial name
- ECAPS (NCT03988569)
- Testing
- audiovisual decision aid
- Where
- United States
- Volunteers
- 158 people
- Sponsor
- Loyola University
Pelvic Organ Prolapse
Risk Factors for Recurrence After Pelvic Reconstruction
232 women underwent transvaginal mesh repair (TVM)with /without transvaginal hysterectomy for symptomatic POP, including group A（accepted herniamesh polypropylene mesh， 117 patients)；group B （underwent biological graft of…
- Trial name
- NCT03457883
- Testing
- herniamesh, biological graft
- Volunteers
- 232 people
- Sponsor
- Nanjing Medical University
Genital Prolapse
Observing Pelvic Organ Prolapse Symptoms And Treatment Outcomes
To prospectively observe the outcomes of surgical prolapse treatment in terms of urinary, bowel, and sexual function, quality of life, patient satisfaction, cost, and achieving patient determined treatment goals.
- Trial name
- NCT00784602
- Where
- United States
- Volunteers
- 301 people
- Sponsor
- Melissa Fischer, MD
Pelvic Organ Prolapse
Smartmesh Technology in Pelvic Floor Repair Procedures
Pelvic organ prolapse repair involves conservative treatments and surgical treatments. Conservative treatments are for patients with moderate prolapse. Treatment of symptomatic prolapse remains essentially surgical.
- Trial name
- Restorelle (NCT03098641)
- Testing
- pelvic organ prolapse repair
- Where
- 16 sites in France
- Volunteers
- 272 people
- Sponsor
- Groupe Hospitalier de la Rochelle Ré Aunis