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Pharmacokinetic Profile of Rosemary Extract Supplement

NCT ID: NCT05931341

Last Updated: 2023-11-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-12-01

Study Completion Date

2024-05-01

Brief Summary

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This study is a clinical trial to observe changes in biomarkers in the blood at pre- and post-supplementation of rosemary extract in healthy adults.

Detailed Description

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Conditions

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Pharmacokinetics

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Dosage 1

Group Type EXPERIMENTAL

Rosemary extract

Intervention Type DIETARY_SUPPLEMENT

Softgel capsule including rosemary extract

Dosage 2

Group Type EXPERIMENTAL

Rosemary extract

Intervention Type DIETARY_SUPPLEMENT

Softgel capsule including rosemary extract

Dosage 3

Group Type EXPERIMENTAL

Rosemary extract

Intervention Type DIETARY_SUPPLEMENT

Softgel capsule including rosemary extract

Interventions

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Rosemary extract

Softgel capsule including rosemary extract

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Healthy subjects aged between 25 and 55 years
* Non-smoker
* Body Mass Index (BMI) between 20 and 30 kg/m2

Exclusion Criteria

* Any history or presence of cardiovascular, pulmonary, gastro-intestinal, hepatic, renal, endocrine, metabolic, hematological, neurologic, psychiatric, systemic or infectious disease
Minimum Eligible Age

25 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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CJ CheilJedang

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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CJFNT000001

Identifier Type: -

Identifier Source: org_study_id