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NCT02200055 · ClinicalTrials.gov registry record · NA
Using Electrical Bioimpedance Assessments to Estimate Perioperative Total Body Water and Postoperative Fluid Need
A NA study, sponsored by United States Naval Medical Center, Portsmouth.
- Completed
- Registry status
- NA
- Development phase
- 86
- Enrollment target
NCT02200055: Completed NA study, sponsored by United States Naval Medical Center, Portsmouth.
NCT02200055 is a NA study that has completed, run by United States Naval Medical Center, Portsmouth. The registered enrollment target is 86 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02200055, a NA study, has completed, sponsored by United States Naval Medical Center, Portsmouth.
- COMPLETED
- Registry status
- NA
- Development phase
- 86 participants
- Enrollment target
Study Summary
Being able to accurately monitor patient bodily fluid levels during and after surgery is very important, as there are a number of complications that can arise if a patient's fluid levels become unbalanced, such as swelling within or pressure on various bodily organ systems. There are several different ways that physicians can monitor a patient's fluid balance during and after surgery, such as measuring the amount of urine output or the use of central venous catheters which measure the pressure in the veins entering the heart. Most of these techniques are invasive since they require tubes to be inserted into the body. A potential alternative would be to use a noninvasive technique such as electrical bioimpedance (BIA). Bioimpedance assessments work by using small electrical currents that can accurately predict both the water surrounding the outside of cells in the body, as well as the total amount of water in the entire body. Electrical bioimpedance assessments have been used to estimate patient swelling following surgery (edema), to measure the volume of blood the heart is pumping out, as well as to calculate body fat percentages. The goal of this study is to relate this technology to fluid shifts within the body that occur as a result of surgery, in particular, major intra-abdominal surgeries. By using bioimpedance during and after surgery, the investigators will compare the data collected with that calculated by using traditional measures of body fluid status, such as urine output and intraoperative blood loss. During the study, the bioimpedance monitors will not replace the standard bodily fluid monitors and will not interfere with their readings. Additionally, the electrical current produced by the bioimpedance monitors is too small for patients to feel and will not interfere with medical devices such as pacemakers.
Primary Outcome
Bioimpedance assessment measurements were recorded for each participant before the surgical procedure
Interventions
- DEVICE Bodystat Quadscan 4000
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 86 participants |
| Start Date | 2012-05 |
| Est. Completion | 2015-07 |
| Phase | NA |
What the finished NCT02200055 record still lists
NCT02200055 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 86 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).
The record links to 0 conditions, and to 1 intervention - of which Bodystat Quadscan 4000 is the first listed.
NCT02200055 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02200055 about?
NCT02200055 is a clinical study titled "Using Electrical Bioimpedance Assessments to Estimate Perioperative Total Body Water and Postoperative Fluid Need". Being able to accurately monitor patient bodily fluid levels during and after surgery is very important, as there are a number of complications that can arise if a patient's fluid levels become unbalanced, such as swelling within or pressure on various bodily organ systems. There are several differe...
What is the current status of trial NCT02200055?
This trial is currently completed. It is a NA study. The enrollment target is 86 participants. The study started on 2012-05. Estimated completion is 2015-07.
What interventions are being tested in trial NCT02200055?
The interventions under investigation include: Bodystat Quadscan 4000 (DEVICE).
Who is sponsoring clinical trial NCT02200055?
This trial is sponsored by United States Naval Medical Center, Portsmouth, which has 7 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02200055's enrollment target sits among peer trials
86 976th of 2000 higher than 1,021 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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