Perminova Respiratory Effort Accuracy Validation 09-12-2013-Rev 2

ClinicalTrials.gov ID: NCT02048436

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Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to validate the accuracy of the Perminova N4 Monitoring system Respiration Rate technology.

Study identification

NCT ID: NCT02048436
Recruitment status: Completed
Study type: Observational
Phase: Not listed
Lead sponsor: Clinimark, LLC; Other
Enrollment: 20 participants

Conditions and interventions

Conditions

Respiratory Rate Accuracy Test

Interventions

Not listed

Eligibility (public fields only)

Age range: 18 Years to 45 Years
Sex: All
Healthy volunteers: Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Sep 2013 (Type not available)
Primary completion: Sep 2013 (Actual)
Completion: Sep 2013 (Actual)
Last update posted: Jan 29, 2014

2013

United States locations

U.S. sites: 1
U.S. states: 1
U.S. cities: 1

Facility	City	State	ZIP	Site status
Clinimark Laboratory	Louisville	Colorado	80027	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT02048436, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Jan 29, 2014 · Synced Nov 15, 2026