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Nitrosomonas Eutropha on Nitrolipids in the Skin

Assessing the Role of Nitrosomonas Eutropha on Nitrolipids in the Skin

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02938650
Enrollment
30
Registered
2016-10-19
Start date
2016-10-31
Completion date
2017-05-31
Last updated
2017-10-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammation

Keywords

nitrolipid, microbiome, inflammation, cytokine

Brief summary

We are looking to see how the addition of nitrosomonas alters the presence of nitrolipids and inflammatory cytokines on the skin.

Detailed description

We are looking to see how the nitrosomonas alters nitrolipids in the skin and the inflammatory cytokines of the skin. We will be using healthy subjects over the course of 2 weeks. Subjects will be using a neutral cleanser for one week prior to the study, skin microbiome,facial photography, lipid and cytokine measurements will be taken at baseline. Subjects will then start using nitrosomonas spray twice daily for one week. There is a portion of the study where the subjects will have skin microbiome, facial photography, lipid measurements, blood pressure measurements and a bloow draw before and after using the nitrosomonas spray for one week.

Interventions

DRUGNitrosomonas eutropha

Subjects will get nitrosomonas eutropha to apply for one week. There is only one arm to this study. Subjects will apply the medication twice a day for one week.

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

15 healthy controls will participate in the study Another set of healthy controls (n=20) will be recruited so that they participate in blood draws.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Those aged 18 and over * Healthy Subjects with clear skin

Exclusion criteria

* Adults unable to consent * Individuals who are not yet adults (infants, children, teenagers) * Pregnant women * Prisoners * Those with acne, eczema, seborrheic dermatitis, rosacea or polycystic ovarian syndrome * Those who have started new oral medication in the last four weeks * Those who have used systemic antibiotics in the last month * Those who have used isotretinoin in the last 6 weeks * Those who have used topical antibiotics or retinoid in the last two weeks. * Those who have autoimmune or metabolic diseases * Those who have changed brands of oral contraceptive within the last four weeks * Those who have chronic medical disorders * Those whose with active skin infections * Concomitant use of nitrates * Concomitant use of anti-hypertensive agents * Those with syncopal episodes

Design outcomes

Primary

MeasureTime frameDescription
Alteration in microbiome diversity and speciesone weekWe will assess the alteration in the skin microbiome over a one week period by assessing the Shannon Diversity Index
Alteration in nitrolipids in the skinone weekwe will assess the change in nitrolipid profile of sebum collections from the skin after application of the nitrosomonas spray.

Secondary

MeasureTime frameDescription
Alteration in blood lipidsone weekwe will assess the change in blood lipids by performing a blood draw
Alteration in skin cytokinesone weekwe will assess the change in skin cytokines with the use of a non-invasive skin collection.
Blood pressure readingsone weekblood pressure readings will be performed throughout the study

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026