Clinical Trials Logo

Clinical Trial Summary

The study is a cohort study. Between 2005 and 2008, a total of 54 patients were examined with ultrasound before and after TOT surgery. The collected data has not been previously published. Now these same patients are to be examined again with a more advanced ultrasound device. The subjects underwent a urogynecological ultrasound examination before surgery and during the follow-up examination 2-3 months after the procedure. In connection with the follow-up examination, the success of the procedure and the satisfaction of the patients have been evaluated. The data was collected between 2005 and 2008, and the purpose is to invite the patients in question to a research visit, so that the long-term effect of the procedure can be evaluated and the position of the band can be determined with a newer technology ultrasound device. The patients' subjective satisfaction with the procedure is assessed using questionnaires.


Clinical Trial Description

The study is a retrospective cohort study. Between 2005 and 2008, a total of 54 patients were examined with ultrasound before and after TOT surgery. The collected data has not been previously published. Now these same patients are to be examined again with a more advanced ultrasound device. The study's inclusion criterion has been stress or mixed incontinence, for which surgical treatment has been indicated. The cough test must have been positive with a 300 ml bladder filling and the separation points <7 in the incontinence charts.. Exclusion criteria included previous incontinence surgery, simultaneous other gynecological surgery, residual urine volume >100 ml, lower urinary tract anomaly, urinary tract infection, more than three urinary tract infections per year, more than second-degree gynecological organ deposition, BMI >35, previous pelvic radiation therapy or active malignancy. Patients with anticoagulant therapy, anticholinergic or duloxetine medication, hemophilia or neurological disease that could cause bladder dysfunction were also not included in the study. Patients who did not understand the importance of research and treatment or who were unable to exercise were also not suitable for the study. The subjects underwent a urogynecological ultrasound examination before surgery and during the follow-up examination 2-3 months after the procedure. In connection with the follow-up examination, the success of the procedure and the satisfaction of the patients have been evaluated. The data was collected between 2005 and 2008, and the purpose is to invite the patients in question to a research visit, so that the long-term effect of the procedure can be evaluated and the position of the band can be determined with a newer technology ultrasound device. The patients' subjective satisfaction with the procedure is assessed using questionnaires. The research visit is carried out at Tyks' Gynecology Outpatient Clinic. During the research visit, the subject is subjected to a gynecological clinical examination, which includes a cough test, and a urogynecological ultrasound examination. Prior to the study visit, the subject is provided with written information about the study and questionnaire forms, which the patient brings with her to the study visit. Written consent to the study has been requested from all women participating in the study. Now the subjects will be asked for their consent again. Permission for the research has been requested from the Ethics Committee. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05787730
Study type Interventional
Source Turku University Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date January 1, 2005
Completion date April 1, 2024

See also
  Status Clinical Trial Phase
Completed NCT06136975 - Low-level Laser Therapy for Genitourinary Syndromes and Stress Urinary Incontinence
Not yet recruiting NCT04390204 - Evaluation of the Effect of a Postural Reflex Rehabilitation Program on a Foam Surface on Stress Urinary Incontinence in Women N/A
Enrolling by invitation NCT05404386 - Effect of Mobile Application on Urinary Incontinence N/A
Completed NCT05096936 - Pilates Method and/or Photobiomodulation in Women With Stress Urinary Incontinence N/A
Completed NCT05751213 - Knack Technique in Post-menopausal Women With Stress Urinary Incontinence N/A
Completed NCT04912830 - Tension Free Vaginal Tape Surgery - Follow up After 10 and 20 Years
Completed NCT05154760 - Effectiveness of Video Conferencing in Urinary Incontinence N/A
Completed NCT04643353 - Use of Non-ablative Vaginal Erbium YAG Laser for the Treatment of Stress Urinary Incontinence. N/A
Completed NCT03763097 - Sonographic Evaluation of the Single-incision Needleless (Contasure-needleless®) Mini-sling Placement to Predict Success
Recruiting NCT03650244 - Nationwide Observation Study to Evaluate the Efficacy and Tolerance of the Adjustable Medical Device REMEEX® in the Treatment of Male Stress Urinary Incontinence
Not yet recruiting NCT06109623 - Correlation Between Changes in Sex Hormone Levels and Stress Urinary Incontinence in Women
Active, not recruiting NCT05390970 - Platelet-Rich Plasma for Stress Urinary Incontinence N/A
Completed NCT03703843 - ARTUS MONO Artificial Urinary Sphincter N/A
Recruiting NCT05828979 - Clinical Investigation to Assess a New Artificial Urinary Sphincter to Treat Urinary Incontinence in Women N/A
Completed NCT05527639 - Kegel Exercises Prior to Strength Training to Improvestress Urinary Incontinence N/A
Completed NCT02407145 - Safety and Efficacy of PVDF (DynaMesh®-SIS Soft) Retropubic Midurethral Slings in Stress Urinary Incontinence in Women
Completed NCT04433715 - Identification of the UDI-6 and the IIQ-7 Cutoff Scores in Urinary Incontinent Women
Completed NCT05529238 - Kegel Exercises for Stress Urinary Incontinence N/A
Completed NCT05721807 - Physiotherapy in Stress Urinary Incontinence N/A
Not yet recruiting NCT06369922 - TENS Analgesia During Outpatient Urethral Bulking for Stress Urinary Incontinence. N/A