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Pelvic Organ Prolapse clinical trials

View clinical trials related to Pelvic Organ Prolapse.

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NCT ID: NCT03973281 Recruiting - Clinical trials for Pelvic Organ Prolapse

EASE: The Materna Prep Pivotal Study

Start date: December 11, 2019
Phase: N/A
Study type: Interventional

This study is designed to evaluate the safety and effectiveness of the Materna Prep Device in reducing pelvic muscle injuries during vaginal delivery. Subjects are randomized to Materna Prep Device or Standard of Care without use of the Materna Prep Device Intervention with the Materna Prep Device is expected to be a one-time use of approximately 30-90 minutes during the 1st stage of labor. Subject participation in the study is targeted to be 12 months from the time of the use of the device during delivery.

NCT ID: NCT03955744 Terminated - Clinical trials for Pelvic Organ Prolapse

3D Translabial Ultrasound for Pessary Size Estimation

Start date: December 18, 2019
Phase: N/A
Study type: Interventional

This is a feasibility study looking at the use of 3D ultrasound with vaginal manometry at various distension volumes to predict the best available pessary for successful fit.

NCT ID: NCT03947164 Recruiting - Prolapse Genital Clinical Trials

iMEA : Comparison of Micro-innervation and Muscle Microstructure of the Anal Levator Muscle Between Patients With Urogenital Prolapse and Those Who Are Asymptomatic

iMEA
Start date: July 17, 2019
Phase: N/A
Study type: Interventional

Pelvic organ prolapse (POP) is defined by the International Continence Society (ICS) as a downward displacement of one or several of the followings: "the anterior wall of the vagina", "the posterior wall of the vagina" or "the cervix". Principal risk factor of the POP is the muscular trauma of the Levator Ani Muscle (LAM) or pelvic nerve injury during vaginal delivery and pregnancy. The POP is a real public health problem. Nearly a quarter of the female population will be affected by this pathology during their lifetime. Also, the POP is responsible for impaired quality of life. POP management is mainly surgical. The LAM is classically described as a striated muscle. In an anatomic study based on female human fetuses, it has been described a new representation of nerve supplying LAM innervation with both autonomic and somatic participation. In a second study, it has been observed within the LAM, a visceral medial area (interface with the pelvic viscera) composed of smooth muscle cells under autonomic nervous control and a lateral parietal area (interface with the bone basin) composed of striated muscle cells under somatic control. Because of the medial localization of these smooth muscle areas, it is hypothesed that the visceral medial zone within the LAM plays a major role in pelvic status maintaining. The main goal is to compare the proportion of smooth muscle cells within the MEA in patients with urogenital prolapse and in asymptomatic ones. The secondary objectives are: - To compare the expression of neurotransmitters within smooth muscle cell areas in patients with POPs and asymptomatic patients. - To compare the proportion of striated muscle cells in MEA in patients with POPs and asymptomatic patients.

NCT ID: NCT03939715 Not yet recruiting - Clinical trials for Pelvic Organ Prolapse

Surgical Intervention With DermaPure vs Native Tissue in Pelvic Organ Prolapse

Start date: April 5, 2020
Phase: Phase 4
Study type: Interventional

Comparing FDA-approved DermaPure with patient's own native tissue surgically for diagnosis of pelvic organ prolapse.

NCT ID: NCT03919123 Recruiting - Quality of Life Clinical Trials

Evaluation of Functional Outcomes After Laparoscopic Promontofixation (PFL).

PeSuLife
Start date: January 1, 2019
Phase:
Study type: Observational

Prolapse of the pelvic organs is a common pathology in women with a strong impact on the quality of life. Its prevalence tends to increase due to increased life expectancy and obesity. The main treatment is surgical and involves all organ specialists dealing with pelvic-perineal functional disorders: urologists, gynecologists, digestive surgeons. Our team wishes to evaluate, on a cohort of patients operated at the Caen University Hospital, the functional uro-gynecologic, digestive and sexual results of pelvic organ prolapse (POP) repair by Laparoscopic Promontofixation (PFL) through symptoms and quality of life validated questionnaires (QoL). The analysis of the responses to these questionnaires will allow us to evaluate the functional results in the short and medium term (from 6 months to 5 years)

NCT ID: NCT03875989 Recruiting - Prolapse, Vaginal Clinical Trials

Vaginal Native Tissues Repair for Pelvic Organ Prolapse

TAPP
Start date: September 27, 2019
Phase: N/A
Study type: Interventional

The aim of the study is to assess at one year the effectiveness of the vaginal patch plastron in comparison of the anterior colporraphy through a combined definition of success: anatomic and functional.

NCT ID: NCT03858673 Completed - Clinical trials for Vault Prolapse, Vaginal

Comparison of PHVP of Different VTH Methods

Start date: January 1, 1986
Phase:
Study type: Observational

To evaluate the post-hysterectomy vault prolapse (PHVP) rates performed using different methods of vaginal total hysterectomy (VTH).

NCT ID: NCT03857724 Not yet recruiting - Clinical trials for Pelvic Organ Prolapse

Three-dimensional Ultrasound Assessment in Cases of Prolapse Surgeries

Start date: July 2019
Phase: N/A
Study type: Interventional

The levator ani muscle seems to play a key role in pelvic floor dysfunction. This muscle has two major components, the pubovisceral (including the pubococcygeus and puborectalis muscles) and the iliococcygeal muscles.Major levator ani defects are associated with pelvic organ prolapse (POP) and POP recurrence

NCT ID: NCT03849157 Recruiting - Clinical trials for Pelvic Organ Prolapse

RCT for Transvaginal Self-cut Mesh vs Mesh-kit for Severe POP

Start date: January 12, 2018
Phase: N/A
Study type: Interventional

Pelvic organ prolapse(POP) is a common health problem and has significant negative effects on woman's quality of life. Transvaginal mesh procedure is a durable reconstructive surgery, but the mesh kits are expensive for underdeveloped countries. Our preliminary trial showed that the use of self-tailored mesh had good success rate (91.8% at 1-year follow-up) and low complication rate. The trial is designed to compare self-tailored titanium-coated polypropylene mesh procedure with mesh-kit in the treatment of POP stage III-IV in terms of efficacy, safety and cost-effective .

NCT ID: NCT03841513 Completed - Clinical trials for Pelvic Organ Prolapse

Minimally Invasive Burch Colposuspension to Reduce Occult Stress Incontinence

MICRO
Start date: January 29, 2019
Phase: N/A
Study type: Interventional

This study evaluates the addition of a laparoscopic Burch colposuspension procedure at the time of laparoscopic sacrocolpopexy to prevent stress urinary incontinence. Half of the participants will undergo Burch colposuspension procedure at the time of sacrocolpopexy, and half of the participants will undergo sacrocolpopexy alone.