Recruiting soon
A Review of Clinical Trial Experiences and Trends From Spinal Cord Injury Patients
What is being collected
Data Collection
Collected from today forward - ProspectiveWho is being recruted
Central Nervous System Diseases+3
+ Nervous System Diseases
+ Spinal Cord Diseases
Over 18 Years
+6 Eligibility Criteria
How is the trial designed
Case-Crossover
Comparing exposures during disease occurrence and non-occurrence in order to assess the short-term effects of triggers.Observational
Study Start: May 2024
Summary
Principal SponsorPower Life Sciences Inc.
Study ContactMichael B Gill
Last updated: January 28, 2026Sourced from a government-validated database.Claim as a partner
Study start date: May 1, 2024
Actual date on which the first participant was enrolled.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.
Official TitleA Review of Clinical Trial Experiences and Trends From Spinal Cord Injury Patients
Principal SponsorPower Life Sciences Inc.
Study ContactMichael B Gill
Last updated: January 28, 2026Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
500 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-Crossover
In this design, participants serve as their own control. Researchers compare a person's exposures just before a health event with exposures at other times, helping identify short-term triggers or risk factors.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Central Nervous System DiseasesNervous System DiseasesSpinal Cord DiseasesSpinal Cord InjuriesWounds and InjuriesTrauma, Nervous System
Criteria
3 inclusion criteria required to participate
Aged ≥ 18 years old
Ability to understand and the willingness to sign a written informed consent document.
Diagnosis of spinal cord injury
3 exclusion criteria prevent from participating
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
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has no location dataSave this study to your profile to know when the location data is available.
Recruiting soonNo study centers