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Splint for Extremity Injury
N/A
Waitlist Available
Led By Philipp Leucht, MD
Research Sponsored by NYU Langone Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 14 days
Awards & highlights
Study Summary
This trial will test whether using a stiff splint after surgery to fix upper-arm fractures leads to less pain than using a soft dressing.
Eligible Conditions
- Extremity Injury
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 14 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~14 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Percent Change in Euro Quality of Life (EQ-5D)
Percent change in Visual Analog Scale (VAS)
Trial Design
2Treatment groups
Active Control
Group I: SplintActive Control1 Intervention
Group II: Soft DressingActive Control1 Intervention
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Who is running the clinical trial?
NYU Langone HealthLead Sponsor
1,373 Previous Clinical Trials
840,957 Total Patients Enrolled
Philipp Leucht, MDPrincipal InvestigatorNew York Langone Medical Center
2 Previous Clinical Trials
190 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Splint
- Group 2: Soft Dressing
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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