Percutaneous Posterior Tibial Nerve Stimulation in Post-operative Voiding Dysfunction After Deep Endometriosis Surgery
Endometriosis, Dysuria
About this trial
This is an interventional treatment trial for Endometriosis focused on measuring deep endometriosis surgery, voiding dysfunction, self-catheterization, posterior tibial nerve stimulation
Eligibility Criteria
Inclusion Criteria:
- Patients who are eligible for the French public healthcare system
- Patients who have given their consent for this research
Exclusion Criteria:
- Patients with cognitive, psychiatric or motor disturbances, that do not allow for independent use of the device
- Patients who do not speak French
- Patients who have had a surgery (bladder or ureters) for endometriosis or any other reason.
- Patients who were participating in another ongoing study, or within the exclusion time stipulated by another study (at the discretion of the investigator)
- Patients unable to give their consent (protected by law: under guardianship / trusteeship)
- Patients who are taking a pharmaceutical treatment for urological problem (anticholinergics, alpha-blockers, prostaglandin)
- Pregnant or breastfeeding women
- Patients with a pacemaker
- Patients with dermatological problem in the area where the device's electrodes have to be installed
Sites / Locations
- Hôpital de la Croix Rousse
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Self-catheterization only
Posterior tibial nerve stimulation + self-catheterization
Patients self-catheterized after each micturition, noting the volume of each spontaneous micturition as well as the volume obtained by subsequent self-catheterization, until self-catheterization is no longer necessary
Patients self-catheterized after each micturition, noting each volume of spontaneous micturition and each volume obtained by self-catheterization. Patients will have 2 sessions per day of PTN (10-20 min) until self-catheterization is no longer necessary.