Nocturia
Conditions
Interventions
Wearing compression stockings during the daytime for one month
Wearing compression stockings during the daytime for one month under different conditions for Intervention 1
Sponsors
Chiba Prefectural Sawara Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with nocturia (two or more night time frequency) Patients aged 20 years or older at the time of consent acquisition Patients who did not refuse participation in this study
Exclusion criteria
Exclusion criteria: Patients with hypersensitivity to the materials in compression stockings Patients with a history of urinary tract infections (e.g., cystitis), urinary tract stones (e.g., ureteral stones, urethral stones, bladder stones), urethral disorders (e.g., urethral polyps, urethral diverticula), or recurrent urinary tract infections (occurring three or more times within 180 days prior to compression stocking use) Patients who underwent pelvic organ surgery (e.g., radical hysterectomy, radical rectal cancer resection, extensive pelvic lymph node dissection) within 30 days prior to compression stocking application Patients who received physical therapy (pelvic floor muscle training, feedback training, biofeedback training, vaginal cones, bladder training, electrical stimulation therapy, magnetic stimulation therapy, etc.) within 30 days prior to wearing compression stockings Patients with severe arterial circulatory disorders, congestive heart failure, or painful cyanotic varicose veins Patients with suppurative phlebitis Other patients deemed unsuitable for this study by the principal investigator or others
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of nighttime frequency in the frequency volume chart | — |
Countries
Japan
Contacts
Public ContactKanya Kaga
Chiba Prefectural Sawara Hospital Department of Urology
Outcome results
None listed