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Prolapse clinical trials

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NCT ID: NCT03378622 Active, not recruiting - Clinical trials for Pelvic Organ Prolapse

Anchor for Robotic Sacrocolpopexy

ARiSe
Start date: November 29, 2017
Phase: Phase 3
Study type: Interventional

1. PRIMARY OBJECTIVE: To assess the effect of absorbable anchor compared to suturing for mesh attachment to vagina in robotic assisted sacrocolpopexy on the length of surgery for this portion of the procedure. 2. SECONDARY OBJECTIVES: i. To assess intraoperative and ii. postoperative complication rates, iii. Intraoperative 10 cm visual analog scale (VAS), to subjectively assess surgeon satisfaction with the technique iv. post-operative Pelvic Organ Prolapse Quantification (POPQ) evaluation for anatomic failure and v. a VAS of the vaginal walls overall appearance

NCT ID: NCT03375879 Recruiting - Blepharoptosis Clinical Trials

Bandage Contact Lens in Post Operative Ptosis Patients

Start date: February 21, 2018
Phase: N/A
Study type: Interventional

This study is being conducted to determine whether the use of bandage contact lens after ptosis surgery provides any benefits for the patient or is unnecessary.

NCT ID: NCT03373812 Not yet recruiting - Involutional Ptosis Clinical Trials

Comparison Between Different Surgical Approaches for the Treatment of INVOLUTIONAL PTOSIS

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

Involutional ptosis is a known eyelid pathology in which the eyelid margin obscures part of the visual axis (MRD1).Patients usually complains of visual field disturbance, deterioration in quality of life and a poor cosmetic appearance. In clinical practice, two main surgical approaches are performed to the repair of involutional ptosis: 1. anterior approach - skin incision and levator muscle insertion advancement. 2. posterior approach - eyelid reversion and tarsectomy Both approaches has its pro's and con's, but to this date, no solid evidence exists to prove which of these techniques is superior in manner of anatomical and functional results. in this prospective study, patients with involutional ptosis will be randomized to each of surgical approaches groups, parameters concerning surgical and post surgical periods will be evaluated.

NCT ID: NCT03349736 Completed - Clinical trials for Urinary Incontinence

Pelvic Floor Muscle Training Programme in Pregnant Nepalese Women- a Feasibility Study

PFMT
Start date: June 25, 2017
Phase: N/A
Study type: Interventional

To our knowledge, no studies in Nepal have reported the feasibility of performing the pelvic floor muscle training in Nepalese women. The aim of the study is to develop and a pelvic floor muscle training programme based on information, education (leaflet, video) and pelvic floor muscles (PFM) exercise in order to prevent or reduce Pelvic organ prolapse(POP) and Urinary Incontinence (UI) in pregnant Nepalese women. The women will receive information (leaflet, video, posters) and guidance on PFMT. Following this, the women are advised to perform daily home PFM exercise Women will record their home PFMT using an exercise diary.

NCT ID: NCT03338400 Completed - Clinical trials for Nausea and Vomiting, Postoperative

Dexamethasone Administration To Improve Patient Recovery In Ambulatory Vaginal Prolapse Surgery: Is There A Role?

Start date: May 1, 2017
Phase: Phase 2
Study type: Interventional

To the investigators knowledge there are no studies in the literature evaluating the effect of Dexamethasone administration on patients undergoing outpatient vaginal prolapse surgeries.

NCT ID: NCT03333811 Not yet recruiting - Vaginal Prolapse Clinical Trials

Sexual Function After Vaginal Repair With Perineorrhaphy

Start date: February 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if perineorrhaphy performed with surgical vaginal prolapse repair improves sexual function.

NCT ID: NCT03322527 Completed - Hemorrhoids Clinical Trials

Evaluation of the Technique LHP (Laser HemorrhoidoPlasty) in Haemorrhoidal Prolapse Mini Invasive Surgery

Start date: December 19, 2016
Phase: N/A
Study type: Observational

Hemorrhoids surgery technics evolved during the past 20 years. Recently a new one using laser have been developped. It aims at reducing the blood flow towards hemorroïdal plexuses by photocoagulating with a fiber laser the terminal branches of the superior rectal artery. The aim is to evaluate the efficacy of this technic and note the post surgery pain and events

NCT ID: NCT03315715 Completed - Clinical trials for Pelvic Organ Prolapse

Dynamic Magnetic Resonance Imaging Before and After Vaginal Prolapse Repair

Start date: March 1, 2018
Phase:
Study type: Observational

This study is to describe the impact of vaginal reconstruction, including an intraperitoneal vaginal vault suspension for pelvic organ prolapse (POP) on pelvic anatomy using dynamic magnetic resonance imaging (MRI) of the pelvis.

NCT ID: NCT03311685 Completed - Clinical trials for Pelvic Organ Prolapse

Vaginal Tactile Imaging for the Assessment of Pelvic Organ Prolapse Repair Efficiency

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

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. Surgical repair will be performed by a single surgeon who will perform either a laparoscopic or vaginal repair.

NCT ID: NCT03307824 Completed - Prolapse Clinical Trials

Operative Time During the Use of the Synthetic Glue IFABONDTM in Laparoscopic Sacrocolpopexy

Procolle 2
Start date: November 20, 2017
Phase: N/A
Study type: Interventional

Laparoscopic sacrocolpopexy has now become the gold standard technique for correction of anterior and apical prolapse. In order to provide an alternative to stapling system and sutures involving vaginal erosion and shrinkage phenomena, there is a technique to fix material meshes by the use of a liquid, tissue, synthetic adhesive and sterile. The investigator hypothesizes that the use of IFABOND ™ adhesive in laparoscopic sacrocolpopexy significantly reduces the time of surgery compared to the classic suture technique. The prospective, randomized, multicenter study therefore aims to compare the time of surgery when using the IFABOND™ synthetic adhesive and the technique by sutures to fix material meshes in laparoscopic sacrocolpopexy.