A Phase 2 interventional study of IR3535 and Permethrin lower dose in Trachoma, sponsored by London School of Hygiene and Tropical Medicine. Completed at 2 sites in 2 countries. Open to participants aged 3 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-04-08.
Sponsored by London School of Hygiene and Tropical Medicine · Phase 2, Interventional, and Prevention
Musca sorbens, a fly that feeds from ocular and nasal discharge on humans, is thought to be the vector of trachoma. We are developing methods of fly control that specifically target this species, in the hope of interrupting Ct transmission. To our knowledge, the use of commercially available insect repellents has never been tested for prevention of Musca sorbens fly-eye contact (i.e. nuisance and landing in the peri-ocular area). Given the likely necessity for prolonged and/or high frequency fly-eye contact for Ct transmission, the reduction of these contacts through the use of fly repellents presents an exciting opportunity for disease control. Here we propose a within-subject, non-masked, trial of the use of commercially available insect repellents against Musca sorbens, with two consecutive participant groups in the laboratory and in the field, and a primary endpoint of measuring the protective efficacy of each repellent product. Repellent products will be chosen from: DEET (N,N-diethyl-3-methylbenzamide), IR3535 (3-[N-butyl-N-acetyl]-aminopropionic acid ethyl ester), Picaridin (2-(2-hydroxyethyl)-1-piperidinecarboxylic acid 1-methylpropyl ester); PMD (para-Menthane-3,8-diol) or permethrin (m-Phenoxybenzyl)-cis,trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate). Products tested will be either (1) topical repellents, or (2) in long-lasting, plastic formulations of repellents that can be worn on the body (wearable repellent technologies). The insect repellent synergist Vanillin (4-Hydroxy-3-methoxybenzaldehyde) may be added to the long-lasting plastic formulations, to improve the duration of protection.
Introduction
Trachoma
Trachoma, a Neglected Tropical Disease (NTD), is the commonest infectious cause of blindness globally, affecting some of the world's poorest communities. Trachoma is caused by repeated ocular infection with the bacterium Chlamydia trachomatis (Ct). Active trachoma begins in childhood with recurrent episodes of follicular conjunctivitis (TF). Chronic inflammation results in immunologically mediated conjunctival scarring and in-turned eyelashes scratching the eye: trichiasis. Eventually sight is lost from irreversible corneal opacification.
Trachoma is currently endemic in 42 countries. The latest estimates from the Global Trachoma Mapping Programme (GTMP) suggest that 180 million people live in trachoma endemic areas and 3.2 million people have trachomatous trichiasis. Around 2.2 million people are visually impaired, of whom 1.2 million are blind. More than 80% of the burden of active trachoma is concentrated in 14 countries, mainly in the Sahel of West Africa and savannahs of East and Central Africa, where water supplies are often scarce.
Trachoma in Ethiopia
Ethiopia is working towards eliminating trachoma by 2020 and began implementing the SAFE strategy as part of national policy in 2003. This has focused on the provision of improved trichiasis surgery, mass drug administration (MDA) and the distribution of public health messages by radio, video, and printed material. From 2001-2015 more than one million trichiasis surgeries were performed, over 170 million doses of azithromycin were given through MDA and more than 24 million latrines were built. Despite these encouraging efforts, trachoma remains a public health problem in many regions of the country, and the burden of disease is far above the elimination targets set by the World Health Organisation (WHO). In many of these communities, despite seven years of annual or biannual high-coverage MDA, the prevalence of TF remains well above threshold for continuing MDA. Data on Ct prevalence after repeated rounds of MDA in hyperendemic settings such as Ethiopia, indicate that reliable long-term control is not consistently achieved, with gradual re-emergence of infection being typical.
Flies and Trachoma
Flies are likely to contribute to Ct transmission in some locations. The three members of the species complex Musca sorbens live in close association with humans across the Old World tropics and sub-tropics, Asia, the Pacific Islands and Australasian regions. The African species, M. sorbens and Musca biseta, are collectively known as The Bazaar fly, but all are also known as 'face flies', because of their habit of aggressively visiting the face to obtain the protein and liquid found in ocular and nasal secretions. When M. sorbens flies visit the face to feed, they can pick up Ct and transfer it on their bodies to another person. This is called mechanical transmission. Sometimes the house fly, Musca domestica, will also display eye-seeking behaviour, but across most trachoma-endemic regions, the vast majority of fly-eye contacts are made by M. sorbens. As well as transmitting trachoma, M. sorbens has been found to harbour enteric pathogens. In communities without adequate sanitation such as pit latrines, filth flies including M. sorbens have direct access to faecal breeding sites in the form of open defection. Here, they contact diarrhoea-causing pathogens, and subsequent contact to children's faces, or contamination of eating surfaces, can lead to pathogen transmission.
Ct can be cultured from guts and limbs of M. domestica fed on Ct-infected egg yolk. Using a tightly controlled guinea pig trachoma model, Chlamydia psittaci was transmitted by flies from infected to uninfected eyes. Infection was established consistently if the time between flies feeding on infected guinea pig ocular secretions and being exposed to uninfected guinea pigs was under one hour. Other, circumstantial, evidence suggests that flies contribute to the transmission of trachoma. In randomised controlled trials, significantly decreasing the M. sorbens population through long-term insecticide spraying led to decreases in the prevalence of clinical signs of active trachoma (infection not tested). However, azithromycin MDA combined with intensive insecticide spraying in other regions had no effect. Multiple transmission routes complicate trachoma epidemiology, and the extent to which flies contribute to transmission must also be dependent on local factors such as fly seasonality, abundance and local environmental factors that influence fly population dynamics. Two studies tested M. sorbens caught leaving faces of Ethiopian children for Ct by polymerase chain reaction (PCR); 15-23% of flies were positive. In The Gambia, Ct positive flies were also caught from children's faces. These data strongly suggest M. sorbens is a vector of trachoma, however, its relative importance probably varies by setting. Although it is probable that flies are involved in transmission, this pathway is poorly understood.
Olfactory cues have been exploited for monitoring and control of vector populations for many years, through the deployment of odour-baited traps. However, in recent years the use of such traps for population suppression of disease vectors has received increased attention, and recently the potential of these methods for malaria control was empirically demonstrated for the first time. One of the most long-standing and established examples of the use of odour-baited traps is the control of tsetse flies and Human African Trypanosomiasis in East Africa.
The investigators have recently conducted field studies in Oromia, Ethiopia, during Phase 1 and Phase 2 of the Stronger SAFE programme, designing a trap from locally sourced and cheaply available materials. The performance of this trap was tested, baited with a commercial lure, relative to several other commercially available fly traps and found to be superior. A major advantage of odour-baited trapping for fly control is that it is not associated with environmental impact concerns. This is in contrast to widespread insecticide spraying, which although has been shown to suppress fly populations very successfully, can be damaging to the environment.
Insect repellents are used world-wide to prevent nuisance biting by non-vector species, and to prevent disease transmission by vectors in disease-endemic regions. Although the use of plants with repellent qualities, either by burning leaves or presenting fresh foliage, is prevalent in many regions, commercially available topical repellents are rarely used by people in low-income and disease-endemic countries. This is because of cost, availability, and the impracticality of a product that requires repeat application. However, when use of insect repellents has been successfully adopted by communities, they have been found to be protective against malaria. Repellents have also been successfully used to control other arthropods of public health significance, including lice and the chigoe flea. A recent review of the evidence that topical insect repellents can be used to protect against clinical malaria or malaria infection found insufficient evidence, and called for better designed trials to generate higher-certainty evidence.
There is growing interest in the use of repellents as personal protection from disease transmission, particularly around the use of insecticide-treated clothing, which can repel biting insects. In these instances, the insecticide used has spatially repellent properties or is a contact irritant, which protects the individual user and the insecticides are not sprayed into the environment. Insecticide-treated clothing has been shown to provide protection from both malaria and leishmaniasis. Another study looked at the use of permethrin-treated headscarves for Afghan women in a Pakistani refugee camp, and found a reduction in the incidence of malaria in people under 20 years old. There is better evidence for the use of insecticide-treated clothing against malaria transmission, particularly advocated in areas where more evidence-based vector control strategies such as long-lasting insecticide-treated bed nets are not appropriate. Again, however, further high-quality studies are required to improve the efficacy evidence base.
Using the M. sorbens colony that the investigators have established at LSHTM, preliminary studies have been conducted that demonstrate M. sorbens are susceptible to most commercially available repellents. The investigators have found evidence that the insecticide permethrin has some spatial repellency to M. sorbens, if impregnated at safe doses into fabric scarves. In areas of high fly density, it is expected that the nuisance caused by these flies may allow such an intervention to be successful, as the immediate benefit of reduced face contact would encourage continued uptake of this intervention. Attractant (odour-baited trap) and repellent (commercially available repellents) technologies will be combined to create a "push-pull" strategy to reduce vector-host contact and attract flies to lethal odour-baited traps that will supress populations.
Research hypothesis
Commercially available insect repellent products can be used to decrease contact to the face, particularly the eyes, nose and mouth, by the eye-seeking fly Musca sorbens. The protection afforded by insect repellents will prevent transmission of Chlamydia trachomatis by infected flies, as well as reducing the nuisance caused by this species.
39 studies on the registry are indexed under Trachoma; 3 are open to participants now.
This study's enrollment of 64 is below the median of 1,300 across 31 interventional studies indexed under Trachoma.
Browse Trachoma studies →London School of Hygiene and Tropical Medicine is the lead sponsor of 298 studies on the registry; 15 are open to participants now.
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Laboratory trial eligibility criteria
Field trial eligibility criteria
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Hypersensitivity
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Other: IR3535 · Other: Permethrin lower dose · Other: Permethrin higher dose
Other: IR3535
Other: Permethrin lower dose
Other: Permethrin higher dose
The topical repellent IR3535 (3-\[N-butyl-N-acetyl\]-aminopropionic acid ethyl ester) only
A fabric scarf, impregnated with the insecticide permethrin (m-Phenoxybenzyl)-cis,trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate) that has contact irritancy/spatial repellency. Dose appropriate to children of 10-20 kg.
A fabric scarf, impregnated with the insecticide permethrin (m-Phenoxybenzyl)-cis,trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate) that has contact irritancy/spatial repellency. Dose appropriate to children more than 20 kg.
Protective Efficacy (PE)
The protection (protective efficacy, p) afforded by a repellent product will be presented as a percentage. p will be estimated by comparing fly-arm contact duration and fly-eye contact frequency, in laboratory and field trials respectively, after application (or wearing) of the repellent product to that during the control period.
Time frame: 2 months
Complete Protection Time (CPT)
Median CPT will be estimated in stage two ('persistence') laboratory trials only, for those repellents that demonstrated more than 30 % PE. The complete protection time for a specific dose will be estimated as the time elapsed until the first fly landing on the arm in each replicate, and based on repeat estimates of CPT, the mCPT will be estimated using a Kaplan-Meier function.
Time frame: 3 months
PDFs hosted by the registry, ClinicalTrials.gov.
Plan to share: Yes — Formal reports will be written for the Ethiopian Federal and Regional health authority and the Federal Ministry of Science and Technology (FMOST). Reports will also be prepared for the Wellcome Trust and The Fred Hollows Foundation (Ethiopia and UK). To ensure operational uptake of the findings of the studies, we intend to present these data at the annual National Trachoma Task Force and NTD Research Symposium (Ethiopia). Additionally, we will present this research at the annual Trachoma Scientific Informal Workshop prior to the WHO GET2020 Alliance meeting. Scientific results will be published in Open Access in peer-reviewed journals and presented at relevant international conferences. The Sensitisation/Community Liaison Team will disseminate the results of the study to the study community in community dialogues and radio broadcasts in conjunction with The Fred Hollows Foundation Ethiopia Communications Team.
Ran from Jan 2019 to primary completion in Dec 2019, 11 months.
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This study is completed, as verified in Apr 2020. You cannot join it, but the record below documents what was studied.
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