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NCT Number: NCT02331979

Improving Bladder Function in SCI by Neuromodulation

This trial will investigate the safety and utility of spinal cord neuromodulation to improve urinary bladder function in the context of spinal cord injury.

Recruiting

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Key information

Age range

18 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

University of California, Los Angeles

Los Angeles, California, 90095, United States

Location status: Recruiting

Location contact

Daniel C Lu, MD PhD

CONTACT

[email protected]

310-267-2975

About this study

This trial will investigate the safety and utility of spinal cord neuromodulation to improve urinary bladder function in the context of spinal cord injury. Neuromodulation will be in the form of transcutaneous electrical stimulation and/or magnetic stimulation.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male 18-45 years;
  • At least 1 year post-injury;
  • Non-progressive SCI at C2-T8 (non-conus injury);
  • Motor Complete ASIA (A or B);
  • Neurogenic bladder requiring clean intermittent straight catheterization;
  • Able to attend twice weekly testing sessions for 6 months.
  • Have intact lower extremity anatomy and able to use lower extremity for assistive standing and stepping.

Exclusion criteria

  • History of autonomic dysreflexia;
  • Ventilator dependency;
  • Musculoskeletal dysfunction, unhealed fracture, pressure ulcer, active infection;
  • Clinically significant depression or ongoing drug abuse;
  • Received botox injection, or bladder surgery (suprapubic access, Brindley procedure, etc.); 6. Prostatic hypertrophy or bladder outlet disorder;
  • Cardiopulmonary disease that precludes lower extremity training or rehabilitation.

Treatment and study plan

Electromagnetic Neuromodulation

Device

Electromagnetic stimulation to neuromodulate the spinal cord in the context of spinal cord injury.

Other names: Transcutaneous Electrical Stimulation, Magnetic Stimulation

Primary outcomes

  1. Urine flow and volume

    Time frame: Months 1-48

Study contacts

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

Daniel Lu, MD PhD

CONTACT

[email protected]

310-825-4321

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Registry information

Important dates

Study start
2015
Primary completion
2026
Study completion
2027
First posted
Jan 6, 2015
Registry last updated
Feb 13, 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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