Clinical Trials Logo

Clinical Trial Summary

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.


Clinical Trial Description

It is a monocentric case-control study (1: 1). The inclusion of cases and witnesses will be prospective. For each case, a witness will be included with matching on parity (0, at least one child). Concerning the age, they will be matched according to the following age groups: 18-39 years old, 40-44 years old, 45-49 years old, 50-54 years old, over 55 years old. For cases and controls, before the intervention, a questioning (age, weight, height, parity, mode of delivery, hormonal status), clinical symptoms of POPs and urinary incontinence, a detailed clinical examination, and an urodynamic assessment (in case of POPs) will be noted. All cases and controls will have an ultrasound guided MEA biopsy. A fine needle will be used. The biopsy (5mm) will interest the medial part located between the vagina and the rectum. Patients will be seen on post-operative visits between 15 days and 2 months after surgery for an examination and clinical examination. From the biopsy, it will be performed a classic staining (Masson's trichrome) and specific immuno-markings to detect all the nerves, and to differentiate parasympathetic autonomic, sympathetic autonomic, erectile, and somatic nerves. Immunostaining for smooth muscle, striated muscle and relaxin system will also be performed. An immunofluorescence technique will be associated. Thus, some additional slides will be reserved for an actomyosin ATPase enzymatic reaction to differentiate muscle fiber types. Treated sections will be digitized with a Hamamatsu slide scanner for subsequent image analysis and analysis. The size of the different types of striated muscle fibers (1, 2a, 2b) will be measured using the NDPview (Hamamatsu) software. The labeling surface of the different antibodies will be quantified objectively by the NIS-Elements Viewer software. Benefits are collective : 1. Clinical impact: Find new medical therapeutic targets and improve rehabilitation techniques. 2. Repercussion in research: - To set up a PHRC with a randomized controlled multicenter study on the comparison of electrical stimulation and voluntary muscular contraction in postpartum with measurement of pelvic floor muscle strength and pelvic-perineal evaluation (search for pelvic prolapse , urinary incontinence). - To improve knowledge of anatomy and physiology of pelvic floor muscles by mapping neurotransmitters in LAM in adult patients with POPs and asymptomatic patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03947164
Study type Interventional
Source Rennes University Hospital
Contact Krystel Nyangoh Timoh, MD
Phone 02.99.28.37.15
Email Krystel.NYANGOH.TIMOH@chu-rennes.fr
Status Recruiting
Phase N/A
Start date July 17, 2019
Completion date July 17, 2024

See also
  Status Clinical Trial Phase
Not yet recruiting NCT06404931 - Transvaginal Human Acellular Dermal Matrix for Prolapse Treatment Phase 2
Completed NCT03077490 - Comparison of Single Versus Multicenter Outcomes for Pelvic Organ Prolapse Repair Using a Mesh-capturing Device
Completed NCT05571072 - Opioid Use After Urogynecologic Procedures: Using a Predictive Calculator N/A
Completed NCT04178473 - Total Versus Subtotal Abdominal Hysterectomy at Time of Abdominal Sacrocolpopexy N/A
Completed NCT03534830 - A Novel Assay for Predicting Surgical Outcomes in Pelvic Organ Prolapse
Completed NCT03772015 - The Change in Vaginal Axis on MRI After Uterus Preserving Laparoscopic Lateral Mesh Suspension
Recruiting NCT06430931 - Biological OviTex Versus Synthetic Graft in Robotic Prolapse Surgery N/A
Terminated NCT03200327 - Comparison of Anterior Vaginal Sacrospinofixation With Laparoscopic Promontofixation for the Treatment of Anterior and Apical Genitourinary Prolapse N/A
Completed NCT05463081 - Clinical Trial of "Magic Gyno" Laser Device N/A