Chronic Hepatitis C InfectionFIVE-CCNCT06899542
HEPATITIS C SCREENING in ADULTS with RISK FACTORS in FIVE CITIES of COLOMBIA'S CARIBBEAN COAST (FIVE-CC)
An observational study of Chronic Hepatitis C Infection, run by Diana Rocio Chavez Bejarano.
Trial summary
Hepatitis C virus (HCV) infection is a significant cause of chronic hepatitis, cirrhosis, and liver cancer (1). The risk of developing cirrhosis in people with chronic HCV infection ranges between 15% and 30% over a period of 20 years (2). Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Chronic Hepatitis C Infection
- How many people
- 4,000 participants
- Where
- No sites listed yet
- Study dates
- Apr 2025to Oct 2025
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: All individuals over the age of 18 with HCV risk factors, including the general population and vulnerable populations at higher risk of chronic hepatitis C infection, recruited from healthcare institutions or during screening campaigns in various settings.
Who may be able to join
- Present at least one of the following risk factors for hepatitis C:
- People over 50 years old with or without risk factors.
- People aged 18 and under 50 years old with risk factors for hepatitis C:
- Individuals who have undergone medical or dental interventions in healthcare settings, Individuals with tattoos, body piercings, or scarification, Individuals co-infected with HIV or hepatitis B, People who inject drugs, Individuals who have used intranasal drugs, Individuals currently or previously incarcerated, Anyone with abnormal liver tests or liver disease, Healthcare students, workers, or public safety personnel (e.g., prison officers or police) who have been exposed to blood at work through needle-stick injuries or sharp objects, Sex workers, Men who have sex with men, Users of port health services, Reinserted or reintegrated individuals, Anyone who has undergone hemodialysis, Individuals who received blood transfusions in Colombia before 1996, People with comorbidities potentially associated with HC: diabetes, ischemic heart disease, cryoglobulinemia, chronic kidney disease, Sjögren's syndrome, hypothyroidism, lichen planus, rheumatoid arthritis, HIV, non-Hodgkin's lymphoma, acute lymphoblastic leukemia, Waldenström's macroglobulinemia, Individuals previously treated for HCV with a sustained viral response, where reinfection is suspected (individuals who continue to engage in risk behaviors). Confirmation testing through HCV viral load (PCR HCV) will be considered for inclusion in the study.
- Agree to participate in the study by signing an informed consent form.
Who cannot join
- Have had hepatitis C within the last three months with a confirmed cure by viral load 12 weeks after treatment or are actively receiving treatment for HCV and do not continue to engage in risk behaviors for reinfection.
- Voluntarily and knowingly refuse to sign the informed consent form or are unable to provide consent due to any type of physical and/or mental disability.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: HEPATITIS C SCREENING in ADULTS with RISK FACTORS in FIVE CITIES of COLOMBIA'S CARIBBEAN COAST
Hepatitis C virus (HCV) infection is a significant cause of chronic hepatitis, cirrhosis, and liver cancer (1). The risk of developing cirrhosis in people with chronic HCV infection ranges between 15% and 30% over a period of 20 years (2).
In 2016, the World Health Organization (WHO) defined the global strategy for eliminating viral hepatitis (Hepatitis C and Hepatitis B). The goals for hepatitis C include a 90% reduction in new cases of infection and a 65% reduction in mortality (3). To achieve this target by 2030, 90% of people living with hepatitis C need to be diagnosed, and 80% of those individuals must receive treatment, along with reducing the incidence of HCV in high-risk groups (4, 5).
Read more
According to 2019 data from the World Health Organization (WHO), 58 million people are living with chronic hepatitis C infection, (2).
Based on information from Colombia's High-Cost Account (CAC), between January 1 and December 31, 2021, 962 people with the infection were identified in Colombia (6). The CAC report for 2021 indicates that the prevalence of chronic HCV was 442, 173, 102, 089, and 25 cases per 100,000 inhabitants for Barranquilla, Soledad, Montería, Cartagena, and Santa Marta, respectively (7). The most common modes of transmission were sexual (72.1%) and parenteral/percutaneous (11.8% of cases) (8).
According to data published by the Polaris Observatory as of 2021, the prevalence in Colombia was estimated at 0.67% (320,000 cases), According to their projections, Colombia is expected to achieve the WHO targets by 2051 under current conditions (9).
Fewer than half of Latin American countries have conducted prevalence studies for HCV, and most of those studies have poor design quality. When extrapolating data from countries with records, the estimated HCV prevalence rate in Latin America is less than 1%. According to the Polaris Observatory's 2019 epidemiological data,only Brazil treated enough patients to achieve a net annual cure rate above 1% of those infected (10).
This study seeks to evaluate the prevalence of hepatitis C through rapid antibody testing and subsequent confirmatory quantitative viral load in the adult population with risk factors in five cities of the Colombian Caribbean coast: Barranquilla, Soledad, Montería, Cartagena, and Santa Marta.
Read the detailed description
As of 2017, according to a WHO report, only 20% of people with HCV worldwide had been diagnosed (18). Micro- elimination strategies targeting small populations, rather than nationwide elimination programs, have been shown to improve diagnosis and treatment rates, yielding significant benefits for expanding the HCV care cascade and achieving WHO goals (14).
In the general population and the most affected populations, HCV screening recommendations from countries like Spain, the United Kingdom, Germany, France, Ireland, Canada, and Australia include population and opportunistic screening. This involves HCV screening in people exposed to risk factors such as intravenous or inhaled drug use, high-risk sexual behavior, HIV/HBV coinfection, aesthetic procedures involving sharp instruments without proper safety precautions, and imprisonment (17). Anyone who received blood transfusions before serological testing of blood donors for HCV, underwent medical or dental procedures in healthcare settings with substandard infection control practices, is also included.
Risk-based screening recommendations, as opposed to population screening, focus efforts and resources, ensuring equity in the design, implementation, and evaluation of HCV screening programs. These allow for addressing access barriers in each context (17). Targeted screening would identify a high number of infected individuals due to the higher infection rate related to risk factors, while simultaneously reducing viral transmission by eliminating HCV from individuals at higher risk of spreading the infection (20).
The study conducted by Rosato et al. (2022) highlight the need to increase awareness among general practitioners and other healthcare specialists who treat patients with different comorbidities to address HCV disease control. This is important as HCV eradication has been shown to significantly improve not only liver disease outcomes but also various comorbidities such as cryoglobulinemic vasculitis, diabetes, cardiovascular, and kidney diseases, etc. (21).
Monitoring the care cascade (CoC) is an essential component of the global response to the hepatitis C virus (HCV) epidemic. The findings allow healthcare decision-makers to determine where the most significant gaps in testing, care linkage, and treatment exist among people with chronic HCV infection (22).
Micro-elimination strategies in populations at high risk of transmitting HCV may contribute to the concept of "treatment as prevention." This concept involves successfully treating an HCV-infected individual who is at risk of transmitting the virus to others, thereby eliminating the possibility of further transmission, achieving "prevention." Due to its potential to prevent additional infections, many of which would incur high costs for treating end-stage liver disease, this approach could be highly cost-effective in the long term (18).
Targeting those at greatest risk of contracting the disease can generate broader community benefits and long-term cost-effectiveness. Supporting this approach to HCV eradication, model studies conducted by Martin and colleagues (2011 and 2013) have indicated that chronic HCV prevalence could be reduced by treating individuals at risk of continuous HCV transmission (23).
Since 2017, Colombia's High-Cost Account (CAC) has monitored identified chronic hepatitis C cases in accordance with Resolution 1692 of 2017, which is part of the strategy for negotiating and centrally purchasing direct-acting antivirals (24).
The most frequently used treatment in 98.2% of cases in the 2019-2020-2021 cohorts was sofosbuvir/velpatasvir, achieving 98.7% effectiveness in 2021 (25).
However, efforts are needed to incentivize screening in people over 50 years old and according to risk exposure, as established by Resolution 3280 of 2018 (25).
- Research Question What is the prevalence of HCV in populations with risk factors for hepatitis C infection, detected through rapid testing in five cities on the Caribbean coast of Colombia? 4. Objectives
General Objective:
Determine the prevalence of HCV in patients with HCV risk factors, detected through opportunistic screening in five cities on the Caribbean coast of Colombia.
Specific Objectives:
- Characterize the sociodemographic profile of the study population.
- Describe the epidemiological characteristics of patients with positive HCV antibodies.
- Determine the proportion of patients with positive HCV antibodies and positive (quantitative) viral load for HCV.
- Conduct an exploratory analysis of the association between positive cases and various HCV infection risk factors.
- Methodology
Study Type:
Descriptive, cross-sectional, multicenter study.
- Conditions
- Chronic Hepatitis C Infection
- Keywords
- Hepatitis C, general population.
- Medical subject headings
- Hepatitis C
What is being measured
The primary outcome is the main question the study is designed to answer.
hepatitis C viremic
HCV RNA detectable by quantitative method.
Measured: 5months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Mar 2025
- Study startApr 2025 (estimated)
- Primary completionSep 2025 (estimated)
- Study completionOct 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Hepatitis C InfectionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 4,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Diana Rocio Chavez Bejarano
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Diana Rocio Chavez Bejarano, Asociación Colombiana de Hepatología
- Investigators
- JAVIER E HERNANDEZ-BLANCO, DR, Principal investigator, Asociación Colombiana de HepatologíaISMAEL YEPES, DR, Principal investigator, Asociación Colombiana de Hepatología
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06899542
- Sponsor's protocol ID
- CO-US-987-7107
- Acronym
- FIVE-CC
- Status last verified
- Mar 2025
- First submitted
- 21 Mar 2025
- Last updated
- 28 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Not included in the approved protocol
Study at a glance
From the registry record, last updated by the sponsor on 28 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- HEPATITIS C SCREENING in ADULTS with RISK FACTORS in FIVE CITIES of COLOMBIA'S CARIBBEAN COAST
- ClinicalTrials.gov ID
- NCT06899542
- Acronym / sponsor ID
- FIVE-CC / CO-US-987-7107
- Conditions
- Chronic Hepatitis C Infection
- Keywords
- Hepatitis C, general population.
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 4,000 participants (estimated)
- Lead sponsor
- Diana Rocio Chavez BejaranoUniversity, hospital or other
- Study start
- Apr 2025 (estimated)
- Primary completion
- Sep 2025 (estimated)
- Study completion
- Oct 2025 (estimated)
- First posted
- 28 Mar 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Hepatitis C virus (HCV) infection is a significant cause of chronic hepatitis, cirrhosis, and liver cancer (1). The risk of developing cirrhosis in people with chronic HCV infection ranges between 15% and 30% over a period of 20 years (2).
In 2016, the World Health Organization (WHO) defined the global strategy for eliminating viral hepatitis (Hepatitis C and Hepatitis B). The goals for hepatitis C include a 90% reduction in new cases of infection and a 65% reduction in mortality (3). To achieve this target by 2030, 90% of people living with hepatitis C need to be diagnosed, and 80% of those individuals must receive treatment, along with reducing the incidence of HCV in high-risk groups (4, 5).
According to 2019 data from the World Health Organization (WHO), 58 million people are living with chronic hepatitis C infection, (2).
Based on information from Colombia's High-Cost Account (CAC), between January 1 and December 31, 2021, 962 people with the infection were identified in Colombia (6). The CAC report for 2021 indicates that the prevalence of chronic HCV was 442, 173, 102, 089, and 25 cases per 100,000 inhabitants for Barranquilla, Soledad, Montería, Cartagena, and Santa Marta, respectively (7). The most common modes of transmission were sexual (72.1%) and parenteral/percutaneous (11.8% of cases) (8).
According to data published by the Polaris Observatory as of 2021, the prevalence in Colombia was estimated at 0.67% (320,000 cases), According to their projections, Colombia is expected to achieve the WHO targets by 2051 under current conditions (9).
Fewer than half of Latin American countries have conducted prevalence studies for HCV, and most of those studies have poor design quality. When extrapolating data from countries with records, the estimated HCV prevalence rate in Latin America is less than 1%. According to the Polaris Observatory's 2019 epidemiological data,only Brazil treated enough patients to achieve a net annual cure rate above 1% of those infected (10).
This study seeks to evaluate the prevalence of hepatitis C through rapid antibody testing and subsequent confirmatory quantitative viral load in the adult population with risk factors in five cities of the Colombian Caribbean coast: Barranquilla, Soledad, Montería, Cartagena, and Santa Marta.
Detailed description
As of 2017, according to a WHO report, only 20% of people with HCV worldwide had been diagnosed (18). Micro- elimination strategies targeting small populations, rather than nationwide elimination programs, have been shown to improve diagnosis and treatment rates, yielding significant benefits for expanding the HCV care cascade and achieving WHO goals (14).
In the general population and the most affected populations, HCV screening recommendations from countries like Spain, the United Kingdom, Germany, France, Ireland, Canada, and Australia include population and opportunistic screening. This involves HCV screening in people exposed to risk factors such as intravenous or inhaled drug use, high-risk sexual behavior, HIV/HBV coinfection, aesthetic procedures involving sharp instruments without proper safety precautions, and imprisonment (17). Anyone who received blood transfusions before serological testing of blood donors for HCV, underwent medical or dental procedures in healthcare settings with substandard infection control practices, is also included.
Risk-based screening recommendations, as opposed to population screening, focus efforts and resources, ensuring equity in the design, implementation, and evaluation of HCV screening programs. These allow for addressing access barriers in each context (17). Targeted screening would identify a high number of infected individuals due to the higher infection rate related to risk factors, while simultaneously reducing viral transmission by eliminating HCV from individuals at higher risk of spreading the infection (20).
The study conducted by Rosato et al. (2022) highlight the need to increase awareness among general practitioners and other healthcare specialists who treat patients with different comorbidities to address HCV disease control. This is important as HCV eradication has been shown to significantly improve not only liver disease outcomes but also various comorbidities such as cryoglobulinemic vasculitis, diabetes, cardiovascular, and kidney diseases, etc. (21).
Monitoring the care cascade (CoC) is an essential component of the global response to the hepatitis C virus (HCV) epidemic. The findings allow healthcare decision-makers to determine where the most significant gaps in testing, care linkage, and treatment exist among people with chronic HCV infection (22).
Micro-elimination strategies in populations at high risk of transmitting HCV may contribute to the concept of "treatment as prevention." This concept involves successfully treating an HCV-infected individual who is at risk of transmitting the virus to others, thereby eliminating the possibility of further transmission, achieving "prevention." Due to its potential to prevent additional infections, many of which would incur high costs for treating end-stage liver disease, this approach could be highly cost-effective in the long term (18).
Targeting those at greatest risk of contracting the disease can generate broader community benefits and long-term cost-effectiveness. Supporting this approach to HCV eradication, model studies conducted by Martin and colleagues (2011 and 2013) have indicated that chronic HCV prevalence could be reduced by treating individuals at risk of continuous HCV transmission (23).
Since 2017, Colombia's High-Cost Account (CAC) has monitored identified chronic hepatitis C cases in accordance with Resolution 1692 of 2017, which is part of the strategy for negotiating and centrally purchasing direct-acting antivirals (24).
The most frequently used treatment in 98.2% of cases in the 2019-2020-2021 cohorts was sofosbuvir/velpatasvir, achieving 98.7% effectiveness in 2021 (25).
However, efforts are needed to incentivize screening in people over 50 years old and according to risk exposure, as established by Resolution 3280 of 2018 (25).
- Research Question What is the prevalence of HCV in populations with risk factors for hepatitis C infection, detected through rapid testing in five cities on the Caribbean coast of Colombia? 4. Objectives
General Objective:
Determine the prevalence of HCV in patients with HCV risk factors, detected through opportunistic screening in five cities on the Caribbean coast of Colombia.
Specific Objectives:
- Characterize the sociodemographic profile of the study population.
- Describe the epidemiological characteristics of patients with positive HCV antibodies.
- Determine the proportion of patients with positive HCV antibodies and positive (quantitative) viral load for HCV.
- Conduct an exploratory analysis of the association between positive cases and various HCV infection risk factors.
- Methodology
Study Type:
Descriptive, cross-sectional, multicenter study.
Study design
- Observational model
- Other
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- All individuals over the age of 18 with HCV risk factors, including the general population and vulnerable populations at higher risk of chronic hepatitis C infection, recruited from healthcare institutions or during screening campaigns in various settings.
Key inclusion criteria (5 listed)
- People over 50 years old with or without risk factors.
- People aged 18 and under 50 years old with risk factors for hepatitis C:
- Individuals who have undergone medical or dental interventions in healthcare settings, Individuals with tattoos, body piercings, or scarification, Individuals co-infected with HIV or hepatitis B, People who inject drugs, Individuals who have used intranasal drugs, Individuals currently or previously incarcerated, Anyone with abnormal liver tests or liver disease, Healthcare students, workers, or public safety personnel (e.g., prison officers or police) who have been exposed to blood at work through needle-stick injuries or sharp objects, Sex workers, Men who have sex with men, Users of port health services, Reinserted or reintegrated individuals, Anyone who has undergone hemodialysis, Individuals who received blood transfusions in Colombia before 1996, People with comorbidities potentially associated with HC: diabetes, ischemic heart disease, cryoglobulinemia, chronic kidney disease, Sjögren's syndrome, hypothyroidism, lichen planus, rheumatoid arthritis, HIV, non-Hodgkin's lymphoma, acute lymphoblastic leukemia, Waldenström's macroglobulinemia, Individuals previously treated for HCV with a sustained viral response, where reinfection is suspected (individuals who continue to engage in risk behaviors). Confirmation testing through HCV viral load (PCR HCV) will be considered for inclusion in the study.
- Agree to participate in the study by signing an informed consent form.
Key exclusion criteria (2 listed)
- Have had hepatitis C within the last three months with a confirmed cure by viral load 12 weeks after treatment or are actively receiving treatment for HCV and do not continue to engage in risk behaviors for reinfection.
- Voluntarily and knowingly refuse to sign the informed consent form or are unable to provide consent due to any type of physical and/or mental disability.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
hepatitis C viremic
Time frame: 5months
HCV RNA detectable by quantitative method.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Mar 2025.
- Individual participant dataSharing planned: No. Not included in the approved protocol
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
JAVIER E HERNANDEZ-BLANCO, DR principal investigator
Asociación Colombiana de Hepatología
ISMAEL YEPES, DR principal investigator
Asociación Colombiana de Hepatología
Questions about this trial
What is this clinical trial studying?
An observational study of Chronic Hepatitis C Infection, run by Diana Rocio Chavez Bejarano.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 28 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact JAVIER E HERNANDEZ-BLANCO, DR (57 3183483581, JHERNANDEZBLANCO@GMAIL.COM), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
hepatitis C viremic (time frame: 5months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Mar 2025.