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NCT06117280 · ClinicalTrials.gov registry record · NA
Effect of Different Dosages of Paraxanthine, the Major Caffeine Metabolite, on Energy and Focus
A NA study of Energy and Focus, sponsored by Iovate Health Sciences International.
- Completed
- Registry status
- NA
- Development phase
- 45
- Enrollment target
- 1
- Study location
NCT06117280 is a NA study of Energy and Focus that has completed, run by Iovate Health Sciences International. The registered enrollment target is 45 participants, below the 859-participant average among 7 other Energy trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06117280, a NA study of Energy and Focus, has completed, sponsored by Iovate Health Sciences International.
- COMPLETED
- Registry status
- NA
- Development phase
- 45 participants
- Enrollment target
- 1
- Study location
Study Summary
Research has shown that acute ingestion of Paraxanthine (1,7-dimethylxanthine, PXN) can enhance various markers of focus, including memory, reaction time, and attention in healthy adults. To assess these effects, this placebo-controlled crossover trial will compare the effects of 200 and 300mg of PXN to a placebo control. Participants will abstain from caffeine for 3 days, before taking the first test/placebo product for 3 consecutive days. Participants will complete questionnaires at 30, 60, 90, and 120 minutes after ingestion on Day 1 and Day 3 of ingestion. Participants will have a 3-day washout period before trialing the next test product/placebo.
Conditions Studied
Interventions
- OTHER Placebo
- OTHER Paraxanthine 200 mg
- OTHER Paraxanthine 300 mg
Study Locations (1)
California
- Citruslabs - Santa Monica
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 45 participants |
| Start Date | 2023-07-18 |
| Est. Completion | 2023-10-20 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06117280
The ClinicalTrials.gov registry entry for NCT06117280 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 859-participant average among 7 other Energy trials with a reported enrollment target (95% lower). The listed sponsor is Iovate Health Sciences International, which has 2 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Energy appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.
NCT06117280 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT06117280 about?
NCT06117280 is a clinical study titled "Effect of Different Dosages of Paraxanthine, the Major Caffeine Metabolite, on Energy and Focus". Research has shown that acute ingestion of Paraxanthine (1,7-dimethylxanthine, PXN) can enhance various markers of focus, including memory, reaction time, and attention in healthy adults. To assess these effects, this placebo-controlled crossover trial will compare the effects of 200 and 300mg of PX...
What is the current status of trial NCT06117280?
This trial is currently completed. It is a NA study. The enrollment target is 45 participants. The study started on 2023-07-18. Estimated completion is 2023-10-20.
What conditions does trial NCT06117280 study?
This clinical trial studies the following conditions: Energy, Focus, Caffeine Withdrawal.
What interventions are being tested in trial NCT06117280?
The interventions under investigation include: Placebo (OTHER), Paraxanthine 200 mg (OTHER), Paraxanthine 300 mg (OTHER).
Who is sponsoring clinical trial NCT06117280?
This trial is sponsored by Iovate Health Sciences International, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06117280 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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