CClinicalTrials.gg
CompletedNCT04144777Updated Feb 15, 2021

Efficacy of Solarplast for Health and Oxidative Stress

An interventional study of Solarplast in Oxidative Stress, Healthy Aging and Skin Health, sponsored by Deerland Enzymes. Completed at 1 site in United States. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-02-15.

Sponsored by Deerland Enzymes · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Jul 2019, registered Oct 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
84
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Solarplast is a unique mixture of antioxidant enzymes and single antioxidant molecules that are capable of attack oxidants that cause damage to the cells in the human body and cause premature aging. This mechanism may provide protection from stress, such as free radicals, heat, infection, as well as reduce inflammation and participate in the repair mechanism of the intestinal tract. Participants will consume Solarplast, or placebo, for 45 days with blood draws at day-0 and -45 in order to assess antioxidant capacity.

Read the detailed description

Solarplast is currently sold on the market, which is a unique mixture of antioxidant enzymes and single antioxidant molecules that attack oxidants through chaperone activity. Chaperones, are naturally occurring proteins that assist the non-covalent folding/unfolding and the assembly/disassembly of other macromolecular structures and can provide stability and restore function of many unfolded proteins. Chaperones may provide protection from stress, such as free radicals, heat, infection, as well as reduce inflammation and participate in the repair mechanism of the intestinal tract. Solarplast is derived from Spinach (Spinacia oleracea), a leafy green vegetable of high nutritional value grown and consumed worldwide. Spinach is rich in iron, vitamin A, riboflavin, and lutein, a carotenoid that acts as a natural antioxidant protecting the body from toxins and free radicals. The potential mechanistic role of Solarplast consists of serving an antioxidant role against peroxyl radicals, hydroxyl radicals, peroxynitrite, super oxide anion, singlet oxygen, among others. Additionally, Solarplast contains photosynthetic complexes with high concentrations of ATP, NADPH, ADP, AMP, NADP, niacin, B12, adenine, and ribose. Therefore, this naturally occurring antioxidant supplement may provide the components required to scavenge free radicals and mitigate oxidative stress with no harmful side effects.

The purpose of this study is to determine the antioxidant and health effects of Solarplast in 40 healthy human subjects, 20 smokers, and 20 pre-diabetics; both male and female (n=80). An equal number of males and females will be recruited for the project. Only participants between the ages of 18 and 55 will be recruited for this research. Smokers and pre-diabetics are known to have increased oxidative stress; therefore, these two populations are being included in this research.

A single capsule of Solarplast containing 100 mg (1 x 10\^6 light converting units (LCU)) is to be consumed once a day per participant for a total of 45 days, following pre-screening and enrollment (detailed below). Twenty healthy (of the 40 healthy) human subjects will be used as control subjects and consume a placebo (maltodextrin - 100 mg).

A medical doctor will approve the enrollment (Dr. Karleena Tuggle) of all participants and oversee this clinical trial.

Participants will be asked to visit the laboratory (KSU Human Performance Laboratory) on 2 separate occasions for blood draws by a CITI approved/IRB approved research team member trained in phlebotomy under the supervision of Dr. VanDusseldorp.

02

Conditions studied

  • Oxidative Stress
  • Healthy Aging
  • Skin Health

Keywords

  • Smokers
  • Prediabetes
  • Cognitive Health
03

In context

Lead sponsor

Deerland Enzymes is the lead sponsor of 7 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Healthy smokers
  • Healthy non-smokers
  • Prediabetics (elevated fasting blood glucose of 100-125mg/dL).

Exclusion criteria

Exclusion Criteria:

  • No specific pulmonary disease
  • No medication or specifically any inhaled bronchodilators or corticosteroids.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
84 participants (actual)

Study arms

  • Experimental
    Treatment

    Subjects will be administered one daily dose of Solarplast (100mg), in a capsule, for 45 days.

    Dietary Supplement: Solarplast

  • No intervention
    Placebo

    Subjects will be administered one daily dose of maltodextrin (100mg), in a capsule, for 45 days.

Interventions

  • Dietary supplementSolarplast

    Subjects will take one capsule of Solarplast (100mg) daily for 45 days.

06

What researchers measure

Primary outcomes

  1. Oxidative Stress

    Analyze change in reactive oxygen species obtained from blood from baseline to 45 days using reactive oxygen species testing kits

    Time frame: 45 days

  2. Blood glucose

    Analyze change in fasting blood glucose obtained from blood from baseline to 45 days using metabolic panel

    Time frame: 45 days

  3. Change in skin health using questionnaires

    Analyze skin health using questionnaires

    Time frame: 45 days

  4. Change in joint pain using questionnaires

    Analyze change in joint pain using questionnaires

    Time frame: 45 days

07

Study locations

1 site
  • Kennesaw State University
    Kennesaw, Georgia 30144, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 15, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04144777
Lead sponsor
Deerland Enzymes
Collaborators
Kennesaw State University
Responsible party
Sponsor
First posted
Oct 30, 2019
Start date
Jul 15, 2019
Primary completion
May 1, 2020
Completion
May 1, 2020
Last update
Feb 15, 2021

Study contacts

Trisha VanDusseldorp, PhD
principal investigator · Kennesaw State University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2019. You cannot join it, but the record below documents what was studied.

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