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Not yet recruiting NCT07140835

Evaluation of the Pedal-Controlled Surgistep Platform to Improve Ergonomics

No phase Interventional Ergonomics

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: SurgiStep Platform, Standard Foot stool.
Who it may be relevant to
Registry conditions: Ergonomics. Basic parameters: 36 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

A Prospective Crossover Study Evaluating the Pedal-Controlled Surgistep Platform to Improve Ergonomics in Neurosurgical Operations

Overview

Primary Aim: Assess improvement in ergonomics and musculoskeletal discomfort with the Surgistep compared to a standard footstool.

Interventions

  • Device SurgiStep Platform
    The Surgistep (pedal-controlled, adjustable platform) allows real-time height adjustment during surgery. The surgeons can adjust the height of the platform.
  • Device Standard Foot stool
    Foot stool is considered as the standard of care during surgery.

Primary outcome measures

  • Rapid Entire Body Assessment (REBA) Scale Score [Time frame: During the surgery upto 60 minutes]
  • Rapid Upper Limb Assessment (RULA) Scale Score [Time frame: During the surgery upto 60 minutes]

Eligibility criteria

Inclusion criteria

  • Regularly perform neurosurgical procedures (cranial/spine)
  • Willing to use both devices (multiple times each).

Exclusion criteria

  • Severe MSK conditions preventing device usage
  • Inability/refusal to participate in observation or surveys.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Crossover
Masking
Open label
Primary purpose
Device feasibility

Study locations

United States · 1 center
  • Stanford Health Care — Palo Alto

Identifiers

NCT: NCT07140835 · 80476

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗