Last reviewed · How we verify
NCT03819023
Validation of RespiLife for Detection of Respiratory Suppression
NA trial testing Respilife monitor in Respiration Disorders in 30 participants. Completed in 20 March 2019.
2 March 2019
Quick facts
| Lead sponsor | Bioresp Technologies, Inc. |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | diagnostic |
| Enrollment | 30 |
| Start date | 20 December 2018 |
| Primary completion | 2 March 2019 |
| Estimated completion | 20 March 2019 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Respilife monitor
Conditions studied
- Respiration Disorders — all drugs for Respiration Disorders →
Sponsor
Bioresp Technologies, Inc.
Who can join
Adults 18 to 80, any sex, with Respiration Disorders. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to evaluate the accuracy of RespiLife diagnostic technology for detection of respiratory rate and oxygen saturation in human subjects. This includes evaluation of Bioresp's RespiLife and its accuracy for measurement of respiratory rate and oxygen saturation.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT03819023
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Respiration Disorders
Currently open trials in the same condition.
- NCT06271213 — The Gut-Lung Axis and Respiratory Illness in Children · recruiting
- NCT06019949 — Spinal Cord Stimulation for Respiratory Rehabilitation in Patients With Chronic Spinal Cord Injury · NA · recruiting
- NCT03709199 — Long Term Follow up of Children Enrolled in the REDvent Study · active not recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03819023 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Bioresp Technologies, Inc.
- Last refreshed: 4 April 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03819023.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing