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Veron Scabies Education and Eradication Program (VSEEP)

Primary Purpose

Scabies

Status
Completed
Phase
Not Applicable
Locations
Dominican Republic
Study Type
Interventional
Intervention
Ivermectin
Permethrin 5% lotion
Sponsored by
Edward Via Virginia College of Osteopathic Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Scabies focused on measuring Scabies, Ivermectin, Lindane, Mass Eradication

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

IVERMECTIN ARM:

  • able to swallow pills
  • no known allergy to Ivermectin
  • not pregnant
  • not breastfeeding
  • 5 years or older
  • taller than 90cm
  • willingness to participate in study and give written consent

PERMETHRIN ARM:

  • no known allergy to Permethrin 5% lotion
  • able to apply lotion to self or to other person if a child
  • pregnant
  • breastfeeding
  • younger than 5 years
  • shorter than 90cm
  • willingness to participate in study and give written consent

Exclusion Criteria:

IVERMECTIN ARM:

  • unable to swallow pills
  • allergy to Ivermectin
  • pregnant
  • breastfeeding
  • younger than 5 years
  • shorter than 90cm
  • unwilling to participate in study or give written consent

PERMETHRIN ARM:

  • unable to apply lotion to self
  • allergy to Permethrin 5% lotion
  • not pregnant
  • not breastfeeding
  • 5 years or older
  • taller than 90cm
  • unwilling to participate in study or give written consent

Sites / Locations

  • Barrio Nuevo

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Ivermectin

Permethrin

Arm Description

Non-pregnant, non-breastfeeding, taller than 90cm and 5 years or older

Pregnant, breastfeeding, children under 90cm or under 5 years old

Outcomes

Primary Outcome Measures

Scabies incidence

Secondary Outcome Measures

Scabies-induced skin abscess incidence
Incidence of Lindane prescription and use
Incidence of Ivermectin prescription and use
Scabies disease, treatment, and prevention awareness

Full Information

First Posted
January 16, 2008
Last Updated
July 18, 2019
Sponsor
Edward Via Virginia College of Osteopathic Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT00604084
Brief Title
Veron Scabies Education and Eradication Program
Acronym
VSEEP
Official Title
Veron Scabies Education and Eradication Program
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
May 2007 (undefined)
Primary Completion Date
May 2008 (Actual)
Study Completion Date
May 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Edward Via Virginia College of Osteopathic Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this project is to develop a community scabies eradication and education program for the highly endemic areas surrounding the Veron community on the eastern tip of the Dominican Republic. It proposes the use of oral Ivermectin as a replacement for topical Lindane--a readily available medical formulation, pesticide, and environmental toxin that is reported to be banned in the Dominican Republic as well as over 80 other countries throughout the world.
Detailed Description
Introduction The Secretaría de Estado de Salud Pública y Asistencia Social public health clinic in Veron, Dominican Republic continually reports a subjectively high prevalence and incidence of scabies infections among its general patient population without any means of direct measurement, proper intervention, or control, raising concerns that long-term infestation may lead to multiple other secondary medical and environmental problems. The purpose of this project is to develop a community scabies eradication and education program for the highly endemic areas surrounding the Veron community. It proposes the use of oral Ivermectin as a replacement for topical Lindane, a readily available and prescribed pesticide and environmental toxin that is reportedly banned for all uses in the Dominican Republic as well as over 80 other countries throughout the world (Boffa, Brough, & Ead, 1995; Davies, Dedhia, Mergade, Banquet, & Maibach, 1983). Ivermectin, on the other hand, is a remarkably safe, effective, cost-comparative oral medication with a substantially broader scope of coverage, duration of effectiveness, and ease of delivery and compliance when compared to Lindane, as well as over 20 years of use in global mass eradication campaigns for other parasites on the order of more than 50 million doses to date (Alexander, Bockarie, Kastens, Kazra, & Alpers, 1998; del Guidice, Chosidow, & Caumes, 2003; Madan, Jaskiran, Gupta, & Gupta, 2001). Specific program goals include: the quantification of community disease prevalence, a statistically significant reduction in both scabies incidence as well as secondary disease sequelae, improved community scabies awareness and prevention abilities, and decreased environmental impact on the Veron area by eliminating the use of Lindane for scabies treatment. The research is designed to employ a door-to-door survey and treatment campaign in a typical Veron neighborhood aimed at evaluating and treating every member in this target population to create a mass prophylaxis that breaks the parasite-host cycle. Another round of treatment will occur 6 months later, per pharmacologic dosage interval recommendations (del Guidice et al., 2003). Individual and group scabies education programs will occur at the Veron clinic, as well as at the local schools to target the highly susceptible youth populations throughout the Veron area. Incidence measurements will occur on a monthly basis for one year after program start, coinciding with two 6-month treatment intervals. At the end of one year, final scabies prevalence and incidence data will be evaluated for statistical significance. While mass treatments will cease at this time, oral Ivermectin will become the standard of care for ectoparasite coverage at the Veron clinic assuming a statistically significant reduction in scabies prevalence is achieved. To date, no mass scabies eradication programs using oral Ivermectin have been reported in the Caribbean, despite it remarkable success in other countries against scabies as well as other parasites, namely onchocerciasis and filariasis (Walker & Johnstone, 2000; Walton & Holt, 2004). This project has the potential to be an important contribution to the effort to eradicate a source of significant morbidity for both the people of Veron and the global community as a whole. Methodology The Veron Scabies Eradication and Education Program will obtain all its priority population data via door-to-door interviews within the Barrio Nuevo neighborhood. A survey team of medical personnel will walk door-to-door program in an attempt to survey and treat every inhabitant of Barrio Nuevo, unless there is refusal or absolute contraindications. Subjects will first be informed of the program and its intent, asked to sign a letter of patient confidentiality, and assigned a number identifier for tracking purposes. After consent is obtained, a survey will be administered to collect basic demographic information, scabies knowledge indicators, as well as pertinent past and current medical history related to scabies infection and contraindications to treatment with Ivermectin. The subject will then be asked to undergo a brief skin exam that assesses scabies infectivity and results recorded using the following criteria: the presence of erythematous popular, vesicular, pustular, or bullous lesions associated with itching. Information will be recorded and used to guide treatment protocol. After the skin exam, subjects will be instructed on scabies medical treatment and prevention, given a patient information and education pamphlet, asked if they have any specific questions or concerns, informed of ongoing community scabies education workshops at the clinic, and instructed to return to the clinic in 2 weeks if they have an active scabies infection. Otherwise, they will be informed that the researchers will return to their neighborhood each month to collect more information and in 6 months to administer another treatment. Finally, the subject will be given 200μg/kg oral Ivermectin dosed by height if they are male or non-pregnant/non-lactating female, 5 years of age or older, and taller than 90 cm. If the subject is a female and of childbearing age (still menstruating on a monthly basis), not currently menstruating, not able to show proof of using oral contraceptives (birth control pills) or injectable contraceptives (scheduled Depo Provera), not surgically sterile (hysterectomy or tubal ligation) they will be asked to undergo a rapid urine pregnancy test. If the test is negative they will be given 200μg/kg oral Ivermectin dosed by height. If the subject is knowingly pregnant or lactating, the rapid pregnancy test is positive, or a child under 5 years and shorter than 90 cm they will be instructed on how to properly use Permethrin 5% lotion and given a 60gm bottle. This protocol will be followed until every household is visited and treated within Barrio Nuevo at time = 0 and again at time = 6 months. Investigators will conduct monthly scabies incidence surveys via door-to-door skin checks within Barrio Nuevo looking for current scabies symptomatology and recording results on the form described above. At the end of one year, final scabies prevalence and incidence data will be evaluated for statistical significance. While mass treatments will cease at this time, oral Ivermectin will become the standard of care for ectoparasite coverage at the Veron clinic assuming a statistically significant reduction in scabies prevalence is achieved.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Scabies
Keywords
Scabies, Ivermectin, Lindane, Mass Eradication

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
1057 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ivermectin
Arm Type
Experimental
Arm Description
Non-pregnant, non-breastfeeding, taller than 90cm and 5 years or older
Arm Title
Permethrin
Arm Type
Experimental
Arm Description
Pregnant, breastfeeding, children under 90cm or under 5 years old
Intervention Type
Drug
Intervention Name(s)
Ivermectin
Other Intervention Name(s)
Ivermectina
Intervention Description
Ivermectin 200ug/kg, 1 dose Q 6 months x 2, total duration = 12 months
Intervention Type
Drug
Intervention Name(s)
Permethrin 5% lotion
Other Intervention Name(s)
Permethrina locion
Intervention Description
apply lotion to entire body, excluding head, at bedtime, rinse off following morning, wait one week, repeat application for a total of 2 applications, PRN frequency, NMT 6 applications in 12 months, total duration = 12 months.
Primary Outcome Measure Information:
Title
Scabies incidence
Time Frame
monthly
Secondary Outcome Measure Information:
Title
Scabies-induced skin abscess incidence
Time Frame
monthly
Title
Incidence of Lindane prescription and use
Time Frame
monthly
Title
Incidence of Ivermectin prescription and use
Time Frame
monthly
Title
Scabies disease, treatment, and prevention awareness
Time Frame
monthly

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: IVERMECTIN ARM: able to swallow pills no known allergy to Ivermectin not pregnant not breastfeeding 5 years or older taller than 90cm willingness to participate in study and give written consent PERMETHRIN ARM: no known allergy to Permethrin 5% lotion able to apply lotion to self or to other person if a child pregnant breastfeeding younger than 5 years shorter than 90cm willingness to participate in study and give written consent Exclusion Criteria: IVERMECTIN ARM: unable to swallow pills allergy to Ivermectin pregnant breastfeeding younger than 5 years shorter than 90cm unwilling to participate in study or give written consent PERMETHRIN ARM: unable to apply lotion to self allergy to Permethrin 5% lotion not pregnant not breastfeeding 5 years or older taller than 90cm unwilling to participate in study or give written consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeremy J White, DO
Organizational Affiliation
Virginia College of Osteopathic Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dean Sutphin, PhD
Organizational Affiliation
Virginia College of Osteopathic Medicine
Official's Role
Study Chair
Facility Information:
Facility Name
Barrio Nuevo
City
Veron
State/Province
La Altagracia
Country
Dominican Republic

12. IPD Sharing Statement

Citations:
PubMed Identifier
8547026
Citation
Boffa MJ, Brough PA, Ead RD. Lindane neurotoxicity. Br J Dermatol. 1995 Dec;133(6):1013. doi: 10.1111/j.1365-2133.1995.tb06950.x. No abstract available.
Results Reference
background
PubMed Identifier
6186202
Citation
Davies JE, Dedhia HV, Morgade C, Barquet A, Maibach HI. Lindane poisonings. Arch Dermatol. 1983 Feb;119(2):142-4. doi: 10.1001/archderm.1983.01650260050017.
Results Reference
background
PubMed Identifier
9861413
Citation
Alexander ND, Bockarie MJ, Kastens WA, Kazura JW, Alpers MP. Absence of ivermectin-associated excess deaths. Trans R Soc Trop Med Hyg. 1998 May-Jun;92(3):342. doi: 10.1016/s0035-9203(98)91035-5. No abstract available.
Results Reference
background
PubMed Identifier
12852376
Citation
del Giudice P, Chosidow O, Caumes E. Ivermectin in dermatology. J Drugs Dermatol. 2003 Jan;2(1):13-21.
Results Reference
background
PubMed Identifier
11603388
Citation
Madan V, Jaskiran K, Gupta U, Gupta DK. Oral ivermectin in scabies patients: a comparison with 1% topical lindane lotion. J Dermatol. 2001 Sep;28(9):481-4. doi: 10.1111/j.1346-8138.2001.tb00015.x.
Results Reference
background
PubMed Identifier
10908470
Citation
Walker GJ, Johnstone PW. Interventions for treating scabies. Cochrane Database Syst Rev. 2000;(3):CD000320. doi: 10.1002/14651858.CD000320.
Results Reference
background
PubMed Identifier
15504541
Citation
Walton SF, Holt DC, Currie BJ, Kemp DJ. Scabies: new future for a neglected disease. Adv Parasitol. 2004;57:309-76. doi: 10.1016/S0065-308X(04)57005-7.
Results Reference
background

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Veron Scabies Education and Eradication Program

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