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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05313945
Other study ID # 69HCL21_0171
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 21, 2022
Est. completion date August 5, 2024

Study information

Verified date July 2023
Source Hospices Civils de Lyon
Contact Camille BENETON, Nurse
Phone 0472119111
Email camille.beneton@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In usual practice, the removal of the bladder catheter is performed by a nurse a few days after the surgery. The nurse deflates the balloon and removes the catheter from the urethra by manual traction. To date, there are no solid data on the impact of passive catheter removal on patient satisfaction. It is therefore necessary to estimate the effect on patient satisfaction of active catheter removal by a nurse versus passive catheter removal under gravity. The effect on pain and anxiety will also be compared between the two techniques. The methodology used was that of an open-label randomized controlled trial.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date August 5, 2024
Est. primary completion date August 5, 2024
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Male = 18 years old 2. With an indwelling urinary catheter placed after any of the following procedures: A uro-endoscopic surgery from the list below: - Endoscopic prostate resection (or transurethral prostate resection). - Laser prostate enucleation - Prostate thermotherapy by radiofrequency - A high-intensity focused ultrasound treatment for prostate cancer - Cervico-prostatic incision or internal urethrotomy - Endoscopic/Transurethral Resection of Bladder Tumor (TURBT) - Surgical treatment of bladder stones, ureter stones (rigid ureteroscopy) and kidney stones (flexible ureteroscopy with laser stone fragmentation) 3. Patient who has given written consent to participate Exclusion Criteria: 1. Patient who is unable to perform intimate hygiene alone in a standing position 2. Patient with a painful genital lesion 3. Patient with an extended pelvic pathology 4. Need to remove the indwelling urinary catheter at the patient's home instead of hospital 5. Patient under guardianship or curator 6. Patient unable to understand the objectives of the study or unwilling to comply with postoperative instructions

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Passive indwelling urinary catheter removal
After washing the patient's perineal area with water and mild soap, the nurse deflates the indwelling urinary catheter balloon and instructs the patient to take a shower (standing). During this time, the catheter will fall under gravity.
Active indwelling catheter removal by a nurse
After washing the patient's perineal area with water and mild soap, the nurse deflates the balloon and removes the catheter from the urethra by manual traction.

Locations

Country Name City State
France CHU Grenoble Grenoble
France Hôpita Edouard Herriot Lyon

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient satisfaction score Patient satisfaction score using a numerical rating scale (NRS) from the minimum value 0 (The worse score) to the maximum value 10 (The better Score) Within one hour after indwelling urinary catheter removal at day 0
Secondary The pain experienced by patients The pain experienced by patients will be measured using a numerical scale (EN) ranging from the minimum value 0 (The better score) to the maximum value 10 (The worse Score) Prior to catheter removal (within 30 minutes before the start of the procedure) and in the immediate aftermath (within one hour after the removal of the catheter)
Secondary The anxiety experienced by patients The anxiety experienced by patients will be measured using a numerical scale (EN) ranging from the minimum value 0 (The better score) to the maximum value 10 (The worse Score) Prior to catheter removal (within 30 minutes before the start of the procedure) and in the immediate aftermath (within one hour after the removal of the catheter)
Secondary Patient satisfaction Patient satisfaction will be evaluated using a satisfaction questionnaire without score at Day 0, at Day 2, at Day 15
Secondary Patient satisfaction Patient satisfaction score using a numerical rating scale (NRS) from the minimum value 0 (The worse score) to the maximum value 10 (The better Score) at Day 2, at Day 15
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