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NCT05545930 · ClinicalTrials.gov registry record · NA
Analysis of Red Blood Cell Integrity and Efficiency of Recovery Using a Novel Surgical Sponge-Blood Recovery Device (ProCell)
A NA study of Blood Recovery, sponsored by University Hospitals Cleveland Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT05545930 is a NA study of Blood Recovery that is actively recruiting participants, run by University Hospitals Cleveland Medical Center. The registered enrollment target is 20 participants. The trial reports 1 study location across 1 state.
The verdict
NCT05545930, a NA study of Blood Recovery, is actively recruiting participants, sponsored by University Hospitals Cleveland Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this research study is to compare two methods of recovering blood from surgical sponges used during heart and lung surgeries. The two methods are: 1) manually wringing sponges by hand, and 2) automated wringing sponges by an FDA approved suction device. Both methods are already in use in heart and lung surgeries at University Hospitals at the discretion of the surgeon.
Conditions Studied
Interventions
- PROCEDURE Hand Wrung
- DEVICE ProCell Wrung
Study Locations (1)
Ohio
- University Hospitals Cleveland Medical Center - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2022-09-20 |
| Est. Completion | 2026-07-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05545930
The ClinicalTrials.gov registry entry for NCT05545930 describes a study currently listed as recruiting, 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 Hospitals Cleveland Medical Center, which has 230 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Blood Recovery appearing as the primary indexed condition, and to 2 interventions - of which Hand Wrung is the first listed.
NCT05545930 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT05545930 about?
NCT05545930 is a clinical study titled "Analysis of Red Blood Cell Integrity and Efficiency of Recovery Using a Novel Surgical Sponge-Blood Recovery Device (ProCell)". The purpose of this research study is to compare two methods of recovering blood from surgical sponges used during heart and lung surgeries. The two methods are: 1) manually wringing sponges by hand, and 2) automated wringing sponges by an FDA approved suction device. Both methods are already in use...
What is the current status of trial NCT05545930?
This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2022-09-20. Estimated completion is 2026-07-01.
What conditions does trial NCT05545930 study?
This clinical trial studies the following conditions: Blood Recovery.
What interventions are being tested in trial NCT05545930?
The interventions under investigation include: Hand Wrung (PROCEDURE), ProCell Wrung (DEVICE).
Who is sponsoring clinical trial NCT05545930?
This trial is sponsored by University Hospitals Cleveland Medical Center, which has 230 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05545930 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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