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Pilot Study of Efficacy of Nail Gel in Finger Nail Surface Abnormality

Pilot Study of Efficacy of Nail Gel Containing Artemisia Abrotanum Extract and Glycerin in Finger Nail Surface Abnormality

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02582762
Enrollment
20
Registered
2015-10-21
Start date
2015-09-30
Completion date
2016-06-30
Last updated
2015-10-21

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

Conditions

Nail Abnormalities

Keywords

Nail gel, Nail surface abnormality, Efficacy

Brief summary

Nail surface abnormalities is any conditions that affect the nail matrix or nail bed which cause nail plates grow defectively. Common nail surface abnormalities are pitting nails, longitudinal ridging, and transverse ridging/Beau's line. Aging nails usually have nail surface abnormalities as well. Nail gels are artificial nails used widely for aesthetic purposes. Although, their cosmetic use is increasing with day by day, their usefulness in conditions such as nail biting, brittle nails, and ingrown toe nails has been reported. Moreover, a previous study reported the benefits of nail gels in terms of improving nail surface abnormalities like pitting nails, trachyonychia, and onychoschizia. This study was conducted to evaluate the efficacy of nail gel containing Glycerin which has humectant effect and Artemisia Abrotanum extract which has anti-fungal/bacterial activities in finger nail surface abnormalities.

Detailed description

Evaluation of nail surface abnormality can be done by using Visiometer® (bioengineering measurement) and dermoscope. Both techniques are non-invasive. Artemisia Abrotanum extract has been used as ingredient in cosmetic products and its safety has been declared. Undesirable events from external using products containing this substance have never been reported yet. Nail gel product in this study has been approved as a cosmetic product by Food and Drug Administration of Thailand (Thai FDA).

Interventions

DRUGNail gel

apply nail gel on affected nails twice daily for 2 months

Sponsors

Mahidol University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

1. Age 18 years old or above 2. Being diagnosed nail surface abnormalities stably more than 3 months

Exclusion criteria

1. Having severe or uncontrolled concomitant diseases 2. Having nail infection 3. History of manicure within the last 1 month 4. Use of Biotin or other nail modifying drugs within the previous 3 months 5. Pregnancy or lactation

Design outcomes

Primary

MeasureTime frameDescription
Improvement overall nail surface abnormalities2 weeks and 8 weeksNumber of nails of each participant with change/improvement nail surface using clinical assessment

Secondary

MeasureTime frameDescription
Improvement roughness of nail surface abnormalities2 weeks, and 8 weeksNumber of nails of each participant with change/improvement nail surface using bioengineering measurement
Increase nail hydration2 weeks, and 8 weeksNumber of nails of each participant with the increase of nail hydration using bioengineering measurement
Patients's satisfaction2 weeks and 8 weeksgood patients's satisfaction outcome by self-questionnaire

Countries

Thailand

Contacts

Primary ContactSumanas Bunyaratavej, MD
consultskin@yahoo.com6624194333

Outcome results

None listed

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