- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03127670
Effect of Solanum Melongena Extract in the Treatment of Arsenical Skin Lesion
July 12, 2018 updated by: Prof. Mir Misbahuddin, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
Solanum melongena is a common vegetable contains phytochemicals which prevent, reduce or delay the oxidation of DNA and alter the cellular signal transduction pathways controlling cell proliferation and apoptosis of human cancer.
The skin of Solanum melongena peel contains nasunin an anthocyanins and chlorogenic acid which have anti-inflammatory, antioxidant, antimutagenic and antiangiogenic properties.
Extract of Solanum melongena is used in actinic keratosis and Squamous cell carcinoma of the skin.
This study will determine any change in arsenical skin lesion after administrating Solanum melongena extract cream.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Bangladesh is grappling with the world greatest ever environmental health disaster in history.
About three decades, more than thirty millions people subsistence with this problem without any potential treatment.
So, now arsenic crisis as a major issue and becomes a demand of era to find out the way to solve this problem.
Chronic ingestion of arsenic contaminated water is a silent killer of the human because even it may cause death by carcinoma.
Arsenic has an affinity to keratin-rich tissue like skin, hair, nail due to the presence of sulphydryl group, as a consequence, they manifest of clinical symptoms like hyperpigmentation or melanosis, diffuse dark brown spot of skin or characteristic rain drop appearance over the trunks, limbs; keratosis.
Even due to prolong exposure to arsenic e.g.
invasive skin lesion as Bown's disease and squamous cell carcinoma appear.
Arsenic as neglected disease arsenic patients has no established treatment except preventive and supportive treatment of melanosis by drinking arsenic free water and salicylic acid as keratolytic substance.
But the malignant condition of arsenic skin lesion treatment is not yet documented.
Solanum melongena belongs to Leptostemonum Clade (the "spine" solanums) species-rice in solanaceae.
It also called brinjal or eggplant.
Solanum melongena is a common vegetable contains phytochemicals which prevent, reduce or delay the oxidation of DNA and alter the cellular signal transduction pathways controlling cell proliferation and apoptosis of human cancer.
Polyphenols of Solanum melongena exhibit an anticancer effect both in vitro and in vivo experiments.
Polyphenol reduces scavenge free radicals, induce apoptosis, inhibit cell proliferation and angiogenesis and exhibit phytoestrogen activity.
On other hand, they suppress the NF-κB and the activating protein (AP-1), inhibit the mitogen-activated proteins (MAPKs), the protein kinase and growth factor receptor-mediated pathways which are involved in cell cycle arrest and possess anti-inflammatory properties.
Solanum melongena has solasodine glycoalkaloids which are cytotoxic and bind with endogenous endocytic lectin of cancer cell membrane and induce apoptosis and cell death both in vivo and in vitro.
The skin of Solanum melongena peel contains nasunin an anthocyanins and chlorogenic acid which have anti-inflammatory, antioxidant, antimutagenic and antiangiogenic properties.
It has a cytotoxic effect on brine shrimp.
Therefore, this study will be conducted to determine is there any change in the patient with arsenical skin lesions before and after application of topical Solanum melongena extract cream.
Twenty-five patients with arsenical skin lesions will be recruited on the basis of inclusion and exclusion criteria after IRB approval.
The patients will be applied Solanum melongena extract cream twice daily for 12 weeks without any interruption.
Water and nails samples will be collected for confirming the diagnosis.
Blood samples will be collected before and after treatment to evaluate the liver and renal function tests.
So, this study will determine any change in arsenical skin lesion after administrating Solanum melongena extract cream.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Faridpur, Bangladesh, 7830
- Bhanga
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age: 18-60 years
- Sex: Both male and female
- Arsenicosis: Severe arsenical skin lesions with Bowen's disease or Squamous cell carcinoma
- Drinking arsenic contaminated water (> 50 µg/L) for more than 6 months
- Patient voluntarily agreed to participate
- Patient who understood the instruction of applying medicine and apply it as he or she will be instructed
Exclusion Criteria:
- Age: Less than 18 and above 60 years
- Expectant, Pregnant and lactating mother
- Major health problems Tuberculosis, Hepatic diseases, Renal diseases, Systamic lupus erythrometosis,
- Rheumatoid arthritis
- Patient with other skin diseases like ectopic dermatitis, psoriasis, eczema, drug allergy
- Food allergy of Solanum melongena
- Patient who received treatment within last three months
- Patient with Bowen disease and Squamous cell carcinoma due to other cause
- Patient did not voluntarily agree to participants
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Solanum melongena peel extract 0.05%
25 Patients Solanum melongena peel extract 0.05% Twice daily applied topically for 12 weeks
|
Administered topically twice daily for 12 weeks
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in palmer arsenical keratosis
Time Frame: Clinical outcome [Time Frame:[0 week (baseline),12 weeks (end)] [Safety Issue: No]] [Safety Issue: No]]
|
Size of keratotic lesion will be decreased
|
Clinical outcome [Time Frame:[0 week (baseline),12 weeks (end)] [Safety Issue: No]] [Safety Issue: No]]
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in the liver function test
Time Frame: Change in lesion size [ Time Frame: [0 week (baseline), 12 weeks (end)] [Safety Issue: No]] [Safety Issue: No]]
|
Abnormal liver function tests will be returned toward normal
|
Change in lesion size [ Time Frame: [0 week (baseline), 12 weeks (end)] [Safety Issue: No]] [Safety Issue: No]]
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
November 14, 2016
Primary Completion (ACTUAL)
December 31, 2017
Study Completion (ACTUAL)
December 31, 2017
Study Registration Dates
First Submitted
April 12, 2017
First Submitted That Met QC Criteria
April 20, 2017
First Posted (ACTUAL)
April 25, 2017
Study Record Updates
Last Update Posted (ACTUAL)
July 13, 2018
Last Update Submitted That Met QC Criteria
July 12, 2018
Last Verified
July 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BSMMU-012-CT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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