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Fasting Mimicking Diet for Skin

N/A
Waitlist Available
Led By Summer Acevedo, PhD
Research Sponsored by L-Nutra Inc
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 0 (baseline) and day 71
Awards & highlights

Study Summary

This trial is testing the effects of a 5-day meal kit on the facial skin of women with mild to moderate skin concerns.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 0 (baseline) and day 71
This trial's timeline: 3 weeks for screening, Varies for treatment, and day 0 (baseline) and day 71 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Secondary outcome measures
Clinical grading of the facial skin
Digital Imaging
Digital Imaging by VISIA
+3 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Fasting Mimicking DietExperimental Treatment1 Intervention
Use the test products, ProLon(TM) Fasting Mimicking Diet, during the scheduled 5-day period in place of the usual meals (breakfast, lunch, dinner, snack) according to the instructions. Use the test product for 5 days for 3 cycles, beginning on day 1, day 30, and day 60.
Group II: ControlActive Control1 Intervention
No usage instructions. Continue regular eating habits for the duration of the study.

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Who is running the clinical trial?

L-Nutra IncLead Sponsor
7 Previous Clinical Trials
589 Total Patients Enrolled
Summer Acevedo, PhDPrincipal InvestigatorSGS Stephens, Inc
1 Previous Clinical Trials
41 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~14 spots leftby Apr 2025