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Analyzing Clinical Research Participation of Patients With Spinal Cord Injury

P

Power Life Sciences

Status

Not yet enrolling

Conditions

Spinal Cord Injuries

Study type

Observational

Funder types

Industry

Identifiers

NCT05831163
83050803

Details and patient eligibility

About

The percentages of participants in clinical studies haven't always been perfectly representative of a particular group.

This research examines the variables that affect a patient's choice to enroll in, discontinue participation in, or resume participation in a clinical trial for spinal cord injury.

It will also try to analyze data from the perspective of different demographic groups to check for recurring trends which might yield insights for the sake of future spinal cord injury research.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged ≥ 18 years old
  • Ability to understand and the willingness to sign a written informed consent document.
  • Diagnosis of spinal cord injury

Exclusion criteria

  • Is pregnant, breastfeeding or expecting to conceive within the projected duration of the study
  • Has a serious medical or psychiatric illness likely to interfere with participation in this clinical study.
  • Inability to provide written informed consent

Trial design

Trial documents
1

Trial contacts and locations

0

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Central trial contact

Michael B Gill

Data sourced from clinicaltrials.gov

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