NCT07173517

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
268

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 7, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

September 15, 2025

Completed
16 days until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2026

Completed
Last Updated

September 15, 2025

Status Verified

July 1, 2025

Enrollment Period

7 months

First QC Date

September 7, 2025

Last Update Submit

September 7, 2025

Conditions

Keywords

neurogenic lower urinary tract dysfunctioncost-savingssacral neuromodulationrechargeable

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

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Qilu Hospital

Jinan, Shandong, China

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

No biological samples were involved and only patient information was collected

Central Study Contacts

Yan Li, Ph.D degree

CONTACT

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

Locations