The Evaluation of Potential Zika, Chikungunya, and Dengue Infections in Mexico
NCT ID: NCT02831699
Last Updated: 2020-12-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
600 participants
OBSERVATIONAL
2016-06-21
2019-01-25
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Subjects with Guillain Barré with potential exposure to Zika virus are of special interest given the severity of disease. Subjects with Guillian Barré do not need to have a preceding illness suggestive of Zika or other viruses. As there are few subjects with Guillain Barré, subjects will be enrolled in two ways - a prospective cohort for subjects with acute Guillain Barré, and a cohort for subjects that had Guillain Barré in the last several years. Data collected systematically from these cohorts will improve the understanding of Zika/Chikungunya/Dengue virus infections.
There are many uncertainties about the number of subjects that meet this case definition. There are limits to the ability to enroll based on staffing and other resources. If there are many cases, an emphasis will be placed on enrolling pregnant subjects and adults with neurologic complications that meet the case definition, as this is the area of highest clinical need. If there are few pregnant women or subjects with neurologic problems that can be enrolled, then any adults or children meeting the criteria can be enrolled. Not all cohorts will be active at all sites, based on the type of facility and type of patients typically seen. If sufficient numbers of certain populations are enrolled (i.e. children born to women infected with Zika), the protocol may be amended to study those populations in more detail.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Febrile Rash
No interventions assigned to this group
Household
No interventions assigned to this group
Guillain-Barré prospective
No interventions assigned to this group
Prior Guillain-Barré
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
1. Meeting the WHO/PAHO case definition, as defined as (a and b and c):
1. One or both of the following primary signs:
* Rash
* Elevated body temperature (\> 37.2 °C) AND
2. One or more of the following symptoms (not explained by other medical conditions):
* Arthralgia
* Myalgia
* Non-purulent conjunctivitis or conjunctival hyperemia
* Headache
* Malaise AND
3. Onset of illness in the last 7 days
2. Modified case definition (a and b):
1. Any two of the following:
* Rash
* Elevated body temperature (\> 37.2 °C)
* Arthralgia
* Myalgia
* Non-purulent conjunctivitis or conjunctival hyperemia
* Headache
* Malaise AND
2. Onset of illness in the last 7 days
1. 1 year of age and older, and
2. Either live in the same household as a subject enrolled into the febrile rash cohort OR live in the same household as a subject who is experiencing an illness similar to Zika (fever and rash as previously described), regardless if said subject is enrolled in the study.
Either confirmed or suspected Guillain-Barré (areflexic flaccid paralysis) as defined either of the following:
1. Confirmed Guillain-Barré
1. Acute onset of weakness or paralysis (from baseline to full weakness in 20 days)
2. Weakness is symmetrical
3. Areflexic (reflexes are 0/4)
2. Suspected Guillain-Barré
1. Acute onset of illness
2. Areflexic flaccid paralysis
1. Confirmed Guillain-Barré
1. Acute onset of weakness or paralysis (from baseline to full weakness in 7 days)
2. Weakness is symmetrical
3. Areflexic (reflexes are 0/4)
4. Diagnosis since January 2014
2. Suspected Guillain-Barré
1. Acute onset of illness
2. Areflexic flaccid paralysis
3. Clinical diagnosis of Guillain-Barré
4. Diagnosis since January 2014
1 Year
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Secretaria de Salud, Mexico
OTHER_GOV
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Mexican Emerging Infectious Diseases Clinical Research Network
NETWORK
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sophia Siddiqui
Role: STUDY_CHAIR
National Institute of Allergy and Infectious Diseases (NIAID)
Guillermo Ruiz-Palacios
Role: STUDY_CHAIR
Mexican Emerging Infectious Diseases Clinical Research Network
Pablo Francisco Belaunzarán Zamudio
Role: PRINCIPAL_INVESTIGATOR
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hospital General de Tapachula
Tapachula, Chiapas, Mexico
Hospital Regional de Alta Especialidad Ciudad Salud
Chiapas, , Mexico
Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado (ISSSTE) Clínica Hospital Dr. Roberto Nettel Flores
Chiapas, , Mexico
Instituto Mexicano del Seguro Social (IMSS) Delegación Estatal / Hospital General de Zona con Medicina Familiar No. 1
Chiapas, , Mexico
Instituto Mexicano del Seguro Social (IMSS) Delegación Estatal / Unidad de Medicina Familiar No. 11
Chiapas, , Mexico
Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
Mexico City, , Mexico
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Belaunzaran-Zamudio PF, Rincon Leon HA, Caballero Sosa S, Ruiz E, Najera Cancino JG, de La Rosa PR, Guerrero Almeida ML, Powers JH 3rd, Beigel JH, Hunsberger S, Trujillo K, Ramos P, Arteaga-Cabello FJ, Lopez-Roblero A, Valdes-Salgado R, Arroyo-Figueroa H, Becerril E, Ruiz-Palacios G; Mexican Emerging Infectious Diseases Clinical Research Network (La Red). Different epidemiological profiles in patients with Zika and dengue infection in Tapachula, Chiapas in Mexico (2016-2018): an observational, prospective cohort study. BMC Infect Dis. 2021 Aug 28;21(1):881. doi: 10.1186/s12879-021-06520-x.
Belaunzaran-Zamudio PF, Ortega-Villa AM, Mimenza-Alvarado AJ, Guerra-De-Blas PDC, Aguilar-Navarro SG, Sepulveda-Delgado J, Hunsberger S, Salgado RV, Ramos-Castaneda J, Rincon Leon HA, Rodriguez de La Rosa P, Najera Cancino JG, Beigel J, Caballero Sosa S, Ruiz Hernandez E, Powers JH 3rd, Ruiz-Palacios GM, Lane C. Comparison of the Impact of Zika and Dengue Virus Infection, and Other Acute Illnesses of Unidentified Origin on Cognitive Functions in a Prospective Cohort in Chiapas Mexico. Front Neurol. 2021 Mar 22;12:631801. doi: 10.3389/fneur.2021.631801. eCollection 2021.
Gouel-Cheron A, Lumbard K, Hunsberger S, Arteaga-Cabello FJ, Beigel J, Belaunzaran-Zamudio PF, Caballero-Sosa S, Escobedo-Lopez K, Ibarra-Gonzalez V, Najera-Cancino JG, Rincon-Leon HA, Ruiz-Hernandez E, Sepulveda-Delgado J, Trujillo-Murillo K, Ruiz-Palacios G. Serial real-time RT-PCR and serology measurements substantially improve Zika and Dengue virus infection classification in a co-circulation area. Antiviral Res. 2019 Dec;172:104638. doi: 10.1016/j.antiviral.2019.104638. Epub 2019 Oct 28.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Zik01
Identifier Type: -
Identifier Source: org_study_id