Opioid-Related Disorders Clinical Trial
Official title:
Development of an Algorithm That Predicts Hypoventilation Due to an Opioid Overdose
NCT number | NCT03845699 |
Other study ID # | 20183438,18C.7 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | May 15, 2019 |
Est. completion date | May 14, 2020 |
RTM Vital Signs, LLC is developing a miniature wearable tracheal sound sensor that communicates with a cell phone containing a machine-learning diagnostic algorithm designed to detect and predict the onset of mild, moderate, and severe hypoventilation (respiratory depression) due to an opioid overdose. The purpose of this clinical trial is to develop/validate diagnostic algorithms capable of detecting/predicting the onset of hypoventilation induced by a controlled intravenous infusion of fentanyl. The wearable sensor and algorithms will provide a series of alerts and alarms to the person, caregiver, and/or emergency personnel.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | May 14, 2020 |
Est. primary completion date | May 14, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 40 Years |
Eligibility |
Inclusion Criteria: 1. Healthy women/men between 18 and 40 years of age. 2. Negative history of drug or alcohol abuse. 3. Negative history of cigarette smoking in previous 6 months. 4. Negative history of active cardiac, vascular, pulmonary, renal, hepatic, nervous, metabolic or immune disease. 5. BMI < 30 Exclusion Criteria: 1. Age < 18 years and > 40 years. 2. Pregnant or planning to become pregnant. 3. Positive history drug or alcohol abuse. 4. Positive drug screen for opioids, benzodiazepines, hypnotics. 5. Positive Drug Abuse Screening Test result (score of 6 or greater). 6. BMI > 30 7. History of sleep apnea. 8. History of cigarette smoking in previous 6 months. 9. History of difficult airway during anesthesia management. 10. History of allergy or skin sensitivity to tape, silicone, fentanyl, chlorhexidine. |
Country | Name | City | State |
---|---|---|---|
United States | Thomas Jefferson University | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
RTM Vital Signs, LLC | Thomas Jefferson University |
United States,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percent Sensitivity and Specificity of Detecting/Predicting the Onset of Mild Hypoventilation due to an Opioid Overdose | The investigators will evaluate the risk-index algorithm's ability to detect/predict at which point during the standardized fentanyl infusion protocol does mild hypoventilation actually occur. Calculate the percent sensitivity and specificity of detecting/predicting the onset of mild hypoventilation (PaCO2- 45 to 50 mm Hg) due to a fentanyl overdose. | 1 to 3 hours | |
Primary | Percent Sensitivity and Specificity of Detecting/Predicting the Onset of Moderate Hypoventilation due to an Opioid Overdose | The investigators will evaluate the risk-index algorithm's ability to detect/predict at which point during the standardized fentanyl infusion protocol does moderate hypoventilation actually occur. Calculate the percent sensitivity and specificity of detecting/predicting the onset of mild hypoventilation (PaCO2- 51 to 60 mm Hg) due to a fentanyl overdose. | 1 to 3 hours | |
Primary | Percent Sensitivity and Specificity of Detecting/Predicting the Onset of Severe Hypoventilation due to an Opioid Overdose | The investigators will evaluate the risk-index algorithm's ability to detect/predict at which point during the standardized fentanyl infusion protocol does severe hypoventilation actually occur. Calculate the percent sensitivity and specificity of detecting/predicting the onset of severe hypoventilation (PaCO2 > 60 mm Hg) due to a fentanyl overdose. | 1 to 3 hours | |
Secondary | Absolute Difference Between Trachea Sound Sensor's Measurements and Reference Sensor Measurements | Correlation between the trachea sound sensor's measurements and the reference sensor measurements of respiratory rate, tidal volume, activity level, and body position during an intravenous infusion of fentanyl (Bland-Altman plot of absolute difference). | 1 to 3 hours |
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