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SKED© for Patient Packaging and Transport Methods

N/A

Waitlist Available

Led By Christopher Davis, MD

Research Sponsored by Wake Forest University Health Sciences

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 minute 5

Awards & highlights

Study Summary

This trial is testing different ways of strapping patients onto a SKED stretcher to see if it affects their respiratory system or how comfortable they are.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ minute 5

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~minute 5

This trial's timeline: 3 weeks for screening, Varies for treatment, and minute 5 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Borg Dyspnea scale

Change in End-Tidal Carbon Dioxide (ETCO2)

Change in Heart Rate

+6 more

Trial Design

4Treatment groups

Experimental Treatment

Group I: Arm1: SKED© only firstExperimental Treatment1 Intervention

Each participant will be packaged using a SKED© system with no assumed spinal injury. Each arm will consist of the same interventions in a specified, but unique order. Arm 1 will be in the following order: SKED© only; SKED©+OSS-II©; SKED©+Vacuum mattress; SKED©+foam padding

Group II: Arm 4: SKED©+foam padding firstExperimental Treatment1 Intervention

Each participant will be packaged using a SKED© system with no assumed spinal injury. Each arm will consist of the same interventions in a specified, but unique order. Arm 4 will be in the following order: SKED©+foam padding, SKED©+Vacuum mattress; SKED© only; SKED©+OSS-II

Each participant will be packaged using a SKED© system with no assumed spinal injury. Each arm will consist of the same interventions in a specified, but unique order. Arm 3 will be in the following order: SKED©+OSS-II©;SKED©+Vacuum mattress; SKED© only; SKED©+foam padding

Each participant will be packaged using a SKED© system with no assumed spinal injury. Each arm will consist of the same interventions in a specified, but unique order. Arm 2 will be in the following order: SKED©+Vacuum mattress; SKED©+OSS-II©; SKED©+foam padding, SKED© only

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Who is running the clinical trial?

Wake Forest University Health SciencesLead Sponsor

1,250 Previous Clinical Trials

1,007,178 Total Patients Enrolled

Christopher Davis, MDPrincipal InvestigatorWake Forest University Health Sciences

~0 spots leftby Jun 2025

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