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NCT Number: NCT04527445

Fluoroscopy Radiation Reduction During Sacral Neuromodulation Lead Placement

Fluoroscopy is performed when placing a lead during a sacral neuromodulation procedure. During lead placement, subjects will receive either conventional or experimental fluoroscopic settings. The radiation exposure will be compared between the two groups.

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Key information

About this study

Patients scheduled for lead implantation during sacral neuromodulation in the operating room and consent will be included in this study. Placement of the lead in the operating room with fluoroscopy is the standard of care in this procedure. Fluoroscopy is performed with a C-arm and there are settings that change the radiation exposure. Patients scheduled to undergo lead placement will be randomized to: a) the investigational (reduced radiation with fluoroscopic settings) or b. the control (conventional fluoroscopy).

The surgeon can change fluoroscopy radiation exposure by changing C-arm settings from the reduced radiation to conventional fluoroscopic options. During the surgery, the surgeon may change the settings from reduced radiation (intervention) to conventional fluoroscopy (control) to safely place lead. The surgeon will use their judgment to optimally place lead and maintain safety during placement. Any deviation from randomization will be recorded.

The intervention arm is defined: Reduced radiation fluoroscopy technique is performed by the C-arm set at 1 pulses-per-second and reduction of current.

The control arm is defined: The standard of care in the conventional fluoroscopy, the C-arm is set at 30 pulses-per-second and the current set at the default.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients undergoing lead implantation for sacral neuromodulation that have overactive bladder as defined by urinary urgency, frequency, nocturia with or without urgency incontinence.

Exclusion criteria

  • neurogenic bladder, BMI >40, or peripheral neuropathy.

Treatment and study plan

Reduced radiation fluoroscopy

Procedure

See previous information about each arm

Conventional fluoroscopy

Procedure

See previous information about each arm

Primary outcomes

  1. Radiation Exposure

    Time frame: At time of procedure

    measure radiation exposure, milligray (mGy)

Secondary outcomes

  1. Optimal lead placement

    Time frame: At time of procedure

    based on intraoperative motor response

  2. Voiding log (Bladder Record)

    Time frame: 3 months after surgery

    Clinical Outcome

  3. Clinical Outcome assessed by validated questionnaire

    Time frame: 3 months after surgery

  4. Inoperative complications

    Time frame: At time of procedure

    surgery complication

  5. Operative times

    Time frame: At time of procedure

    minutes

Study contacts

Contact information is provided by the study sponsor or research team.

Forrest Jellison, MD

CONTACT

[email protected]

909 558-2830

Sponsors and collaborators

Lead sponsor

Loma Linda University

Other

Registry information

Official study title

Reduction in Fluoroscopy Radiation Exposure During Lead Implantation for Sacral Neuromodulation: A Randomized Prospective Study

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Aug 26, 2020
Registry last updated
Mar 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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