Clinical trial
Safety and Efficacy of an Ambulatory Biofeedback Device for Primary Insomnia
NCT00415714 · Helicor, Industry · Unknown status
Key facts
| NCT number | NCT00415714 |
|---|---|
| Title | Safety and Efficacy of an Ambulatory Biofeedback Device for Primary Insomnia |
| Official title | A Randomized Controlled Pilot Trial Testing the Safety and Efficacy of an Ambulatory Biofeedback Device for Primary Insomnia |
| Lead sponsor | Helicor, Industry |
| Status | Unknown status |
| Study type | Interventional |
| Conditions | Primary Insomnia |
| Intervention type | Device |
| Interventions | Portable Biofeedback |
| Enrollment | 132 |
| Start date | Sep 1, 2006 |
| Completion | Oct 1, 2007 |
| First posted | Dec 25, 2006 |
| Last update posted | Jan 29, 2007 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: