Clinical Trials Logo

Prolapse clinical trials

View clinical trials related to Prolapse.

Filter by:

NCT ID: NCT04551859 Not yet recruiting - Apical Prolapse Clinical Trials

Concordance of Pelvic Organ Mobility Measurements Between the Finite Element Model and the Dynamic Pelvic Floor MRI in Patients Undergoing a Sacrospinofixation Surgery

BiomécaRichter
Start date: October 2020
Phase: N/A
Study type: Interventional

The primary objective of this study is to demonstrate the feasibility of using a Finite Element model of pelvic organs by evaluating the concordance of pelvic organ mobility measurements performed by this mechanical model compared to the observations on the post-operative pelvic MRI in patients undergoing a sacrospinofixation surgery

NCT ID: NCT04393194 Not yet recruiting - Clinical trials for Pelvic Floor Prolapse

The Effect of Intra-vaginal Conjugated Estrogen Cream on Ring Pessary Use for Pelvic Organ Prolapse

Start date: May 24, 2020
Phase: Phase 4
Study type: Interventional

The primary purpose of this two-arm randomized clinical trial is to determine if in women desiring use of a pessary for pelvic organ prolapse (POP) and are successfully fit, if 1-year use and patient impression of improvement is superior in women using vaginal estrogen cream versus those using a vaginal placebo cream.

NCT ID: NCT04299334 Not yet recruiting - Clinical trials for Mitral Regurgitation

Neochordae Technique in Mitral Valve Repair

Start date: March 2, 2020
Phase: Phase 1
Study type: Interventional

Mitral valve (MV) repair has turned into a preferable option for surgeons over the MV replacement. Since the 1960s, Surgeons use this technique for more efficiency and durability. On the other hand, the proper determination of length and placement of artificial neochordae is still a challenge beyond this technique. These challenges are still a vital area for research and debate between surgeons and researchers. In our novel technique,Investigators are not depending either on the preoperative investigations or intraoperative reference chordae in the adjustment of the optimal length of the neochordae, however, Researchers depend on the personal adjustment of the chordal length to the prolapsed scallop.

NCT ID: NCT04251923 Not yet recruiting - Quality of Life Clinical Trials

Vaginal Prolapse Surgery Accompanied by Mid Urethral Sling Versus no Sling for Reduction of Postoperative Incontinence

Start date: January 2020
Phase: Phase 2/Phase 3
Study type: Interventional

Prevalence of pelvic organ prolapsed is high in Nepal. After prolapse surgery many patients are affected with incontinence. Incontinence has physical, social and mental effect to the individual. This study is designed to know the role for mid urethral sling during vaginal prolapse surgery to decrease the rate of incontinence after the surgery.

NCT ID: NCT04083703 Not yet recruiting - Clinical trials for Lumbar Disc Herniation

Evaluation of Interbody Cage Insertion in Treatment of Lumbar Disc Prolapse

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

Comparison between discectomy alone and interbody cage insertion in treatment of lumbar disc prolapse

NCT ID: NCT04078802 Not yet recruiting - Vaginal Prolapse Clinical Trials

0050-19-RMB CTIL - VNOTES Compared to VH for Vaginal Apex Prolapse

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

VNOTES (Transvaginal natural orifice transluminal endoscopic surgery) is a relatively new surgery for Hysterectomy and Uterosacral ligament suspension to treat Vaginal prolapse. The investigators wish to run a randomized control trial comparing it to classic Vaginal hysterectomy for the same indication.

NCT ID: NCT04002375 Not yet recruiting - Apical Prolapse Clinical Trials

Posterior Approach for Pectouteropexy

Start date: June 30, 2019
Phase: Phase 4
Study type: Interventional

Pectouteropexy surgery has lower complication rates compared to other sling operations. Sacrocolpopexy is another common procedure for hanging the uterus. Small bowel obstruction, ileus or defecation problems are observed in percentages ranging from 0.1 to 5%. Mesh placed between sacrum and vagina often causes narrowing of the pelvis, adhesions may occur and traumas may occur in hypogastic nerves. However, presacral bleeding, which is the most feared complication of these operations, is a rare but life-threatening condition. In pectouteropexy, it is located away from the bladder, intestine and hypogastric vessels by placing the iliopectineal ligament laterally and eliminates the risk of presacral hemorrhage. In pectouteropexy surgery, the mesh is placed anterior to the cervix. The points emphasized in the criticisms about this technique, inadequate support of the posterior compartment mesh placed in anterior in a future pregnancy is a possible cesarean section and the negative effects on the delivery process. Therefore, a new technique of pectouteropexy surgery to the posterior of the cervix instead of the anterior cervix of the cervix, the sacrouterine ligament to reduce the complications that may occur due to this procedure and this study was planned to increase the effectiveness.

NCT ID: NCT03995797 Not yet recruiting - Clinical trials for Pelvic Organ Prolapse

VESPER: Pelvic Organ Prolapse Study

VESPER:POP
Start date: October 1, 2023
Phase: N/A
Study type: Interventional

Patients seen with Stage 1-2 pelvic organ prolapse (POP) who have failed conservative treatments will be offered to participate in a sham controlled RCT of outpatient therapy with the Fotona Smooth Erbium Yag Laser. Patients will be randomised to either outpatient laser treatments or sham treatments. Patients will be blinded to which arm they have been randomised. Patients will be asked to complete appropriate relevant symptom and quality of life questionnaires and prolapse scoring, prior to treatment and at each monthly treatment and then 6 and 12 months following the final treatment. At 6 months following final treatment, Sham patients will be un-blinded and offered the laser therapy if they wish.

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: 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