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NCT03160170 · ClinicalTrials.gov registry record · NA
Efficacy of Suction Enabled Retraction Device
A NA study, sponsored by University of Miami.
- Terminated
- Registry status
- NA
- Development phase
- 20
- Enrollment target
NCT03160170 is a NA study that was terminated before completion, run by University of Miami. The registered enrollment target is 20 participants.
The verdict
NCT03160170, a NA study, was terminated before completion, sponsored by University of Miami.
- TERMINATED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
Study Summary
This is a prospective randomized controlled trial of the Suction-Integrated Surgical Tissue Elevator \& Retractor \[SISTER\] device to assess: * Effects on operative time and efficiency of exposure in open lumbar spine cases. * Effect on total blood loss during the exposure part of the operation. * Rate of clogging of suction device.
Interventions
- DEVICE SISTER device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2017-06-20 |
| Est. Completion | 2018-12-28 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03160170
The ClinicalTrials.gov registry entry for NCT03160170 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Miami, which has 721 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which SISTER device is the first listed.
NCT03160170 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03160170 about?
NCT03160170 is a clinical study titled "Efficacy of Suction Enabled Retraction Device". This is a prospective randomized controlled trial of the Suction-Integrated Surgical Tissue Elevator \& Retractor \[SISTER\] device to assess: * Effects on operative time and efficiency of exposure in open lumbar spine cases. * Effect on total blood loss during the exposure part of the operation. ...
What is the current status of trial NCT03160170?
This trial is currently terminated. It is a NA study. The enrollment target is 20 participants. The study started on 2017-06-20. Estimated completion is 2018-12-28.
What interventions are being tested in trial NCT03160170?
The interventions under investigation include: SISTER device (DEVICE).
Who is sponsoring clinical trial NCT03160170?
This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.
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