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NCT03678116
Effects of a Thermogenic Dietary Supplement on Metabolic, Hemodynamic, and Mood Responses
NA trial testing Sugar Pill (placebo) in Energy Metabolism in 14 participants. Completed in 31 October 2018.
31 October 2018
Quick facts
| Lead sponsor | University of Mary Hardin-Baylor |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | double |
| Primary purpose | other |
| Enrollment | 14 |
| Start date | 23 July 2018 |
| Primary completion | 31 October 2018 |
| Estimated completion | 31 October 2018 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Sugar Pill (placebo) — full drug profile →
- Caffeine (plus Teacrine and Cayenne)
- Caffeine (plus Teacrine)
Conditions studied
- Energy Metabolism — all drugs for Energy Metabolism →
- Heart Rate — all drugs for Heart Rate →
- Blood Pressure — all drugs for Blood Pressure →
- Mood — all drugs for Mood →
Sponsor
University of Mary Hardin-Baylor
Who can join
Adults 18 to 35, any sex, with Energy Metabolism or Heart Rate. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This a randomized, double blind, placebo controlled, crossover design study which measures the effect of an available thermogenic dietary supplement on resting energy expenditure (REE), blood pressure and heart rate, and mood changes in moderate caffeine consumers. Participants will complete baseline measurements then ingest one of three pills. Once the pill is ingested, subjects will complete four REEs along with heart rate and blood pressure and appropriate questionnaires. Participants will return two more times, each after a one week washout period, and complete the same protocol with the remaining supplements.
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 NCT03678116
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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- Google Scholar
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Other University of Mary Hardin-Baylor trials
Trials by the same sponsor.
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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 NCT03678116 (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 University of Mary Hardin-Baylor
- Last refreshed: 28 March 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/NCT03678116.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing