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The Effectiveness of a Proprietary of a Botanical Extract on Sleep Quality

NCT06894108 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 89

Last updated 2025-09-23

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy and superiority of a botanical based sleep product on sleep quality as compared to melatonin, among healthy female participants.

Conditions

  • Sleep

Interventions

DIETARY_SUPPLEMENT

Proprietary Blend of Botanical Extracts

Participants consumed 2.4ml of the supplement each night before bed.

DIETARY_SUPPLEMENT

Melatonin

Participants consumed 1mg melatonin each night before bed.

Sponsors & Collaborators

  • Nutraceuticals Research Institute

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
35 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-10-01
Primary Completion
2025-03-31
Completion
2025-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06894108 on ClinicalTrials.gov