Cost Profile and Budget Implications of Rechargeable Versus Non-rechargeable Sacral Neuromodulation Devices for Neurogenic Lower Urinary Tract Dysfunction
SNM、NLUTD
1 other identifier
observational
268
1 country
1
Brief Summary
Traditional sacral neuromodulation devices are not rechargeable. In recent years, new rechargeable sacral neuromodulation devices have been developed and put into the market. The aim of this study was to evaluate the cost savings of a rechargeable sacral neuromodulation device versus a non-rechargeable sacral neuromodulation device for the treatment of neurogenic lower urinary tract dysfunction.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 7, 2025
CompletedFirst Posted
Study publicly available on registry
September 15, 2025
CompletedStudy Start
First participant enrolled
October 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedSeptember 15, 2025
July 1, 2025
7 months
September 7, 2025
September 7, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Costs associated with sacral neuromodulation therapy
Costs associated with sacral neuromodulation therapy
From August 2020 to January 2025
Study Arms (2)
rechargeable group
non-rechargeable group
Eligibility Criteria
They were treated with rechargeable or non-rechargeable sacral neuromodulation devices
You may qualify if:
- male and female patients with neurogenic lower urinary tract dysfunction who had failed conventional treatment
- obstructive urinary retention and contraindications to SNM
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Qilu Hospital of Shandong Universitylead
- Aerospace Center Hospitalcollaborator
- Shandong Provincial Hospitalcollaborator
- Second Affiliated Hospital of Xi'an Jiaotong Universitycollaborator
- Beijing Hospitalcollaborator
- Xi'an Honghui Hospitalcollaborator
- The First Affiliated Hospital of Zhengzhou Universitycollaborator
- Second Hospital of Jilin Universitycollaborator
- Sun Yat-Sen Memorial Hospital of Sun Yat-Sen Universitycollaborator
- Tongji Hospitalcollaborator
Study Sites (1)
Qilu Hospital
Jinan, Shandong, China
Biospecimen
No biological samples were involved and only patient information was collected
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 7, 2025
First Posted
September 15, 2025
Study Start
October 1, 2025
Primary Completion
April 30, 2026
Study Completion
April 30, 2026
Last Updated
September 15, 2025
Record last verified: 2025-07