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Combined Effects of Prunus Cerasus and Apocynum Venetum On Sleep and Anxiety in Adults With Insomnia - Trial NCT06299488

Access comprehensive clinical trial information for NCT06299488 through Pure Global AI's free database. This phase not specified trial is sponsored by Lakshmi Nutraceuticals LLC and is currently Completed. The study focuses on Insomnia. Target enrollment is 77 participants.

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NCT06299488
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Trial Details
ClinicalTrials.gov โ€ข NCT06299488
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Combined Effects of Prunus Cerasus and Apocynum Venetum On Sleep and Anxiety in Adults With Insomnia
Combined Effects of Prunus Cerasus (Montmorency Tart Cherry) and Apocynum Venetum (Venetronยฎ) On Sleep and Anxiety in Adults With Insomnia

Study Focus

Insomnia

Sip2Sleep: Montmorency Cherry and Apocynum Venetum

Interventional

other

Sponsor & Location

Lakshmi Nutraceuticals LLC

West Hollywood, United States of America

Timeline & Enrollment

N/A

Apr 05, 2023

Jul 01, 2023

77 participants

Primary Outcome

Subjective Sleep Quality

Summary

Lay Summary: This study is about the effect of using a unique formula called Sip2Sleepยฎ, a
 product currently available on the market which is a combination of montmorency tart cherry
 extract and Venetronยฎ (Apocynum venetum leaf extract) on sleep. The purpose of this study is
 to evaluate the effects of taking this combination product on various aspects of sleep. This
 study is being conducted by People Science, and is sponsored by Lakshmi Nutraceuticals, LLC.
 The information we gather will help inform how people may use Sip2Sleepยฎ to affect the
 quality of sleep.
 
 Participants in this study will complete a number of surveys about their difficulties falling
 asleep and staying asleep (insomnia), their energy level during the day and health status
 regarding their quality of sleep.
 
 There are no major risks associated with this study.

ICD-10 Classifications

Nonorganic insomnia
Disorders of initiating and maintaining sleep [insomnias]
Sleep disorders
Sleep disorder, unspecified
Other sleep disorders

Data Source

ClinicalTrials.gov

NCT06299488

Non-Device Trial