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Effectiveness of Garlic Oil in the Treatment of Arsenical Palmer Keratosis

Effectiveness of Garlic Oil in the Treatment of Arsenical Palmer Keratosis

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01748669
Enrollment
60
Registered
2012-12-12
Start date
2011-10-31
Completion date
2012-07-31
Last updated
2012-12-12

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

Conditions

Chronic Arsenic Poisoning

Keywords

Arsenic, Arsenicosis, Garlic oil, Keratosis

Brief summary

Twenty patients of mild to moderate degree of arsenical palmer keratosis will be treated with garlic oil capsule orally for 12 weeks to examine its effectiveness in reducing body arsenic load and clinical symptoms. Similar treatment with similar number of arsenic exposed controls and healthy volunteers will be included for comparison.

Detailed description

Thousands of Bangladeshi are suffering from arsenic-induced keratosis affecting palms and soles. Palmer keratosis, particularly in young female, affects the socioeconomic condition. Till today there is no effective treatment. Twenty patients of mild to moderate degree of arsenical palmer keratosis will be treated with garlic oil in soft capsule (10 mg/day) orally for 12 weeks. Similar treatment will be given to 20 arsenic exposed controls and 20 healthy volunteers for comparison. The aim of this study is to examine the effectiveness of oral administration of garlic oil to reduce body arsenic load and clinical symptoms of arsenical palmer keratosis.

Interventions

DIETARY_SUPPLEMENTGarlic oil

Oral administration

Sponsors

Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

(Patients): * history of taking arsenic contaminated water (\>50 ppb) for more than 6 months * patients having mild to moderate arsenical keratosis present on palm of the hand * patients those voluntarily agree to participate Inclusion Criteria (Arsenic exposed controls): * family member of the patient * drinking arsenic contaminated water from the same source as patient * those voluntarily agree to participate * no sign/symptom of palmer keratosis Inclusion Criteria (Healthy volunteers): * drinking arsenic safe water (\<50 ppb) * those voluntarily agree to participate

Exclusion criteria

* pregnancy * lactating mother * patient receiving treatment of arsenicosis * any other chronic disease like tuberculosis, diabetes mellitus, bronchial asthma

Design outcomes

Primary

MeasureTime frame
Change in the clinical symptom of keratosis in palm0 week (baseline) to 12 weeks (end)

Secondary

MeasureTime frame
Change in biochemical parameters (blood sugar, cholesterol and transaminase) after treatment0 week (baseline), 12 weeks (end)
Adverse effects following treament0 week (baseline), 12 weeks (end)
Change in the amount of arsenic in nail0 week (baseline), 20 weeks (end)

Countries

Bangladesh

Outcome results

None listed

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