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A randomised, double-blind, controlled study to evaluate the effect of Aloe Vera Examination Gloves, compared to Standard Powder Free Nitrite Examination Gloves, on trans-epidermal water loss and hand dermatitis among health care workers

A randomised, double-blind, controlled study to evaluate the effect of Aloe Vera Examination Gloves, compared to Standard Powder Free Nitrite Examination Gloves, on trans-epidermal water loss and hand dermatitis among health care workers

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001267
Enrollment
Unknown
Registered
2011-03-04
Start date
2011-03-11
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Hand condition

Interventions

1:Gloves with aloe vera for four weeks
2:Gloves with aloe vera for four weeks

Sponsors

Shen Wei, USA, Inc
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: A total of 20 subjects, who fulfil the following inclusion criteria, will be recruited: 1. Female or male health care workers (nurses, nursing students or laboratory personnel) working in a hospital setting; 2. Age 18-60 years (inclusive); 3. Subjects with history of or current dry skin condition or irritant contact dermatitis of hands; 4. Subjects otherwise healthy and free from other sickness and diseases; 5. Female subjects of childbearing potential, who agree to use physician-approved contraceptive regimen during the whole study period; 6. Subjects giving free consent to comply with the scheduled study procedures and clinical evaluations.

Exclusion criteria

Exclusion criteria: 1. Subjects with known allergy to latex; 2. Subjects with known allergy to aloe vera; 3. Subjects suffering from severe contact dermatitis or atopic dermatitis; 4. Subjects suffering from severe allergic skin conditions, psoriasis, urticaria or having skin fissures, excoriations etc. that would, in the opinion of the investigator, not be suitable to participate; 5. Subjects suffering from any active fungal or bacterial infection; 6. Subjects taking oral steroid for any condition or using topical steroid preparations for their hands; 7. Female subjects who are pregnant or lactating; 8. Any criteria which in the opinion of the investigator, suggests that the subjects would not be compliant with the study protocol.

Design outcomes

Primary

MeasureTime frame
Reduction in TEWL from baseline to Day 14, Day 28 ;

Secondary

MeasureTime frame
Reduction of Physician assessed contact dermatitis scores from baseline to Day 14, Day 28 and Day 3 2. Improvement in Subjects assessed skin condition scores from baseline to Day 14, Day 28 and Day 30;

Countries

China

Contacts

Public ContactHon KL
ehon@hotmail.com+852 26322859

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026