Pulmonary ComplicationsPOINTNCT06608849
The Incidence of Pulmonary, Cardiovascular and Renal System Non-communicable Complications Associated With the Post-acute Phase of the Infection by Covid-19
An observational study of Pulmonary Complications and Cardiovascular Complications, run by Hellenic Institute for the Study of Sepsis at 6 sites in Greece.
Trial summary
More than 660 million cases of COVID-19 have been reported worldwide, with 183 million cases in the EU alone. In several people, after recovery, the effects of the first waves of COVID-19 persisted beyond the acute phase and increased the risk of chronic multiorgan symptoms and disease. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Pulmonary Complications, Cardiovascular Complications, Renal Complications
- What is being tested?
- Blood samples and Six-minute walk test, Spirometry, HRCT, Heart ultrasound, Completion of questionnaires of symptoms
- How many people
- 345 participants
- Where
- 6 sitesGreece
- Study dates
- 10 Dec 2024to 4 Nov 2027
- 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: POINT will include patients who have participated in the studies ESCAPE, SAVE, SAVE-MORE and SAVE-LONG. For these patients blood samples and clinical data are already available (Baseline - Year 0 from ESCAPE, SAVE \& SAVE-MORE and Year 1 from SAVE-LONG). POINT needs to enroll three groups of patients (selected by the existing biobank mentioned above, based on the inclusion and exclusion study criteria) to cover the magnitude of the spectrum of COVID-19: * Group A (115 Comparators): Comparators without medical history of acute infection by SARS-CoV-2. * Group B (115 with NO dysfunction): Patients fully recovered by acute COVID-19 who did not present any acute organ injury during acute infection by SARS-CoV-2. * Group C (115 with Dysfunctions): Patients who presented signs of lung, heart, and kidney dysfunction during acute infection by SARS-CoV-2.
Who may be able to join
- Group A (comparators)
- Adults (18 years or more) of both genders
- Negative history of acute COVID-19
- Group B (patients with ΝΟ dysfunction)
- Adults (18 years or more) of both genders
- History of acute COVID-19 hospitalized or non-hospitalized. All cases appearing from start of the pandemic until the last six months may apply
Show all 12Show fewer
- Absence of any current overt organ dysfunction
- Absence of signs of any organ dysfunction during acute COVID-19
- Group C (patients with dysfunctions)
- Adults (18 years or more) of both genders
- History of acute COVID-19 hospitalized or non-hospitalized. All cases appearing from start of the pandemic until the last six months may apply
- Presence of signs of organ dysfunction of the lung, the kidneys or the heart during acute COVID-19
Who cannot join
- Group A (comparators)
- Any other co-existing disorder generating clinical symptoms
- Failure to thrive according to the attending physicians
- Pregnancy or lactation
- Group B (patients with ΝΟ dysfunction)
- Any other co-existing disorder generating clinical symptoms
Show all 19Show fewer
- Failure to thrive according to the attending physicians
- Pregnancy or lactation
- Group C (patients with dysfunctions)
- Any other co-existing disorder generating clinical symptoms
- Medical history of any of:
- stage III or IV chronic obstructive pulmonary disease according to the GOLD criteria
- pulmonary fibrosis or pulmonary hypertension
- stage IV solid tumour malignancy under chemotherapy or radiotherapy
- systemic sclerosis
- congestive heart failure
- stage II, III or IV dyspnoea according to the New York Heart Association classification before the acute COVID-19
- Limited chance of survival for at least six months due to co-existing comorbidity(-ies) according to the judgement of the attending physicians
- Pregnancy or lactation
Trial locations and contacts
6 sites in 1 country. Contact the study team or a site near you to ask about taking part.
6 sites in 1 country
Greece6 sites, 6 recruiting
- Recruiting
10th Department of Pulmonary Medicine, Sotiria Athens Hospital of Chest Diseases
Athens
Dr. Ilias Kainis, 00302107771118, elikas60@gmail.com
- Recruiting
4th Department of Internal Medicine, ATTIKON University General Hospital
Athens
Prof. Evangelos Giamarellos-Bourboulis, 00302105831994, egiamarel@med.uoa.gr
- Recruiting
Obstructive Diseases Clinic, Sotiria Athens Hospital of Chest Diseases
Athens
Assoc. Prof. Nikoletta Rovina, 00302107763452, nikrovina@med.uoa.gr
- Recruiting
Out-patient department of Infectious Diseases, Sotiria Athens Hospital of Chest Diseases
Athens
Assoc. Prof. Garyfallia Poulakou, 00302107763439, gpoulakou@gmail.com
- Recruiting
1st Department of Internal Medicine, Thriasio General Hospital of Elefsina
Elefsina
Dr. Styliani Symbardi, 00302132028497, lianasympa@hotmail.com
- Recruiting
2nd Department of Internal Medicine, Thriasio General Hospital of Elefsina
Elefsina
Dr. Konstantina Iliopoulou, 00302132028441, dr.iliopoulou@gmail.com
About this study
Official title: A Non-interventional, Prospective, Cross-sectional Study of the Incidence of Pulmonary, Cardiovascular and Renal System Non-communicable Complications Associated With the Post-acute Phase of the Infection by Sars-Cov-2
More than 660 million cases of COVID-19 have been reported worldwide, with 183 million cases in the EU alone. In several people, after recovery, the effects of the first waves of COVID-19 persisted beyond the acute phase and increased the risk of chronic multiorgan symptoms and disease. Up to 70% of people affected by COVID-19 showed reduced organ function even four months or more after COVID-19 diagnosis. Such a functional decline is associated with an increased risk of the development of non-communicable diseases (NCDs). Thus, there is an essential need for a better knowledge, tools, clinical guidelines and recommendations that it will make it possible to reduce this overrepresentation of NCDs as a consequence of the post-acute phase (PAP) of COVID-19.
The overall concept underpinning "POINT" is to i) build detailed knowledge on the link between the PAP of COVID-19 caused by previous, current, and future SARS-CoV-2 variants in vaccinated and unvaccinated people, and NCDs, ii) identify robust biomarkers and build predictive tools that help early identification and management of risk of NCDs, and iii) develop guidelines and recommendations for all parts of the healthcare value chain, allowing best prevention and care acknowledging vulnerability. The investigators will focus on the NCDs affecting pulmonary, cardiovascular and renal systems.
Read the detailed description
Post-acute phase of COVID and Non-communicable diseases
Following the emergence of SARS-CoV-2, more than 660 million cases of COVID-19 have been reported worldwide, with 183 million cases in the EU alone. These numbers will continue to grow even after the disease becomes endemic. In some people, after recovery, the effects of the first waves of COVID-19 persisted beyond the acute phase and increased the risk of chronic multiorgan symptoms and disease. Up to 70% of people affected by COVID-19 showed reduced organ function even four months or more after COVID-19 diagnosis. Such a functional decline is associated with an increased risk of the development of non-communicable diseases (NCDs). This is especially true for individuals aged 65 and older as the risk of NCDs increases with age.
Diseases of the pulmonary, cardiovascular, and renal systems are the three major NCDs carrying the most significant burden for the individual as well as society. Studies have documented compromised function of these 3 organ systems in the PAP of COVID-19 in 30%-70% of patients, regardless of the severity of the acute-phase. As homeostasis of these three organs depends on interorgan communication with each other, the impact of PAP of COVID-19 on one will impact the others. The added stress of the PAP of COVID-19 increases the risk of a higher incidence and/or the risk of an accelerated progression of disease.
The prevalence and socioeconomic cost of the three NCDs is already extremely high. Without a strong focus on minimmising the increased risk of incidence and accelerated progression of the NCDs as a result of the PAP of COVID-19, up to 9 million Europeans may be affected and result in an added direct attributable cost of between 19.564 € - 31.064 € per year for each person who develop an NCD.
Beyond state of the art: pulmonary, cardiovascular and renal complications after the PAP of COVID-19
Post-acute COVID-19 and pulmonary complications - Respiratory conditions have been reported as occurring twice as often after severe COVID-19 as in the general population. In a study of 135 individuals, the incidence of impaired lung diffusing capacity (DLCO) and persistent lung damage was demonstrated in 30% of patients 12 months after acute COVID-19. In another study of 142 individuals, pulmonary abnormalities were observed by CT scans in 54% of individuals a year after acute COVID-19.
Post-acute COVID-19 and cardiovascular complications - The PAP of COVID-19 is associated with an increased risk of deep vein thrombosis up to three months after COVID-19 infection, pulmonary embolism up to six months, and a bleeding event up to two months. In a registry study of 153,760 individuals with COVID-19, the 12 month period following the acute phase was characterized by an increased risk and an excess disease burden of cardiovascular diseases, including heart failure, dysrhythmias and stroke. The risks were evident regardless of age, race, sex, and other cardiovascular risk factors. MRI revealed cardiac impairment in 78% of 100 individuals in the PAP of COVID-19.
Post-acute COVID-19 and renal complications - A study of 1733 individuals documented reduced renal function in 35% 6 months after the acute phase of COVID-19 and 13% of patients who did not have acute kidney injury (AKI) during the acute phase showed a disproportionate reduction in renal function during follow-up. A study including \>89,000 individuals revealed an increased risk of adverse renal outcomes in the PAP of COVID-19.
The main unmet needs requiring action at the European level There is an urgent need to enable a better understanding of the causality between PAP of COVID-19 and the increased risk of pulmonary, cardiovascular, and renal complications and thereby an increased risk of onset of disease or aggravation of existing disease. Even though recent studies suggest such a link, there is a need for a more nuanced study of the correlation on much larger cohorts to determine the incidence and risk ratio more accurately. Furthermore, there is a need to compare the outcomes between the early, present, and potential future strains of SARS-CoV-2 variants responsible for the disease. An increased cohort size will also allow a better understanding of the impact of socioeconomic status, difference between sexes, the compounding effects of genotype, pre-existing comorbidities, and use of prescription drugs and of differences between the PAP of early strains of SARS-CoV-2 in mostly unvaccinated individuals compared with current strains in mostly vaccinated people. As this knowledge is currently incomplete, there is an immediate risk that a large part of the European population will not receive optimal and timely care.
Thus far, investigators have concluded that the functional decline of organs caused by COVID-19 cannot be explained by known risk factors. A review of the recent literature suggests that the PAP of COVID-19 is associated with immune dysregulation, elevated levels of autoantibodies, microbiota disruption and clotting and endothelial abnormalities. However, the same review also concludes that the current understanding is not sufficient to improve outcomes and calls for additional research. This underscores the involvement of unidentified molecular mechanisms responsible for the aetiology. A lack of understanding of these inhibits the development of effective biomarkers and drug candidates that allow optimal prediction of the prognosis and treatment of patients following resolution of the initial symptoms of COVID-19.
There is an urgent need for updated clinical practice guidelines and new tools to diagnose and prevent the development and aggravation of NCDs caused by the PAP of COVID-19. Currently, there are very few clinical guidelines and recommendations related to the PAP of COVID-19 and NCDs in general, and there are even fewer clinical guidelines and recommendations that focus on the effects of the PAP of COVID-19 on pulmonary, cardiovascular, and renal health. Modern clinical practice guidelines and recommendations that efficiently bridge the gap between research and current practice are invaluable for securing best quality of care, patient outcomes and cost effectiveness. Unfortunately, the development of a guideline or a recommendation does not necessarily lead to changes in clinical practice. Clinical guidelines and recommendations are not always followed, and it is estimated that approximately 30%-40% of patients receive treatment that is not based on scientific evidence and 20%-25% receive treatments that are not needed or potentially harmful.
- Being tested
- Blood samples, Six-minute walk test, Spirometry, HRCT, Heart ultrasound, Completion of questionnaires of symptoms
- Keywords
- Covid-19, SARS-CoV-2, Pulmonary complications, Cardiovascular complications, Renal complications, Post-acute phase, Non communicable diseases, Biomarkers, Prevention
- Medical subject headings
- COVID-19, Noncommunicable Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Blood samplesOther
Blood sampling for proteomics and transcriptomics, suPAR measurement \& isolation and stimulation of peripheral blood mononuclear cells, eGFR, serum creatinine, cystatin c \& urea
Six-minute walk test, Spirometry, HRCT, Heart ultrasound, Completion of questionnaires of symptomsOther
Spirometry for forced expiratory volume in the first, second, total lung capacity and diffusion capacity of carbon monoxide.
| Study group | Role | What they receive |
|---|---|---|
| Comparators | Comparators without medical history of acute infection by SARS-CoV-2. Receives: Other: Blood samples; Other: Six-minute walk test, Spirometry, HRCT, Heart ultrasound, Completion of questionnaires of symptoms | |
| Participants with NO dysfunction | Patients fully recovered by acute COVID-19 who did not present any acute organ injury during acute infection by SARS-CoV-2. Receives: Other: Blood samples; Other: Six-minute walk test, Spirometry, HRCT, Heart ultrasound, Completion of questionnaires of symptoms | |
| Participants with Dysfunctions | Patients who presented signs of lung, heart, and kidney dysfunction during acute infection by SARS-CoV-2. Receives: Other: Blood samples; Other: Six-minute walk test, Spirometry, HRCT, Heart ultrasound, Completion of questionnaires of symptoms |
What is being measured
The primary outcome is the main question the study is designed to answer.
The incidence of any organ dysfunction during the first 48 months among patients of group C compared to group B
This is a composite endpoint which includes the development of chronic failures of at least one of lung, heart and/or kidneys
Measured: From enrollment to Month 48
Secondary outcomes (5)
The incidence of any organ dysfunction during the first 48 months among patients of group C compared to group A.
This is a composite endpoint which includes the development of chronic failures of at least one of lung, heart and/or kidneys.
Measured: From enrollment to Month 48.
The incidence of any organ dysfunction during the first 48 months among patients of group B compared to group A.
This is a composite endpoint which includes the development of chronic failures of at least one of lung, heart and/or kidneys.
Measured: From enrollment to Month 48.
The incidence of chronic lung failure during the first 48 months among patients of group C compared to group B.
Measured: From enrollment to Month 48.
• The incidence of chronic heart failure during the first 48 months among patients of group C compared to group B.
Measured: From enrollment to Month 48.
• The incidence of chronic renal disease during the first 48 months among patients of group C compared to group B.
Measured: From enrollment to Month 48.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Sep 2024
- Study start10 Dec 2024
- Primary completion4 Nov 2027 (estimated)
- Study completion4 Nov 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pulmonary ComplicationsStudies 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
- Cross-sectional
- Enrolment
- 345 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hellenic Institute for the Study of Sepsis
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Prof. Evangelos Giamarellos-Bourboulis, Study chair, Hellenic Institute for the Study of Sepsis
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06608849
- Sponsor's protocol ID
- POINT
- Acronym
- POINT
- Status last verified
- Nov 2025
- First submitted
- 17 Sep 2024
- Last updated
- 17 Nov 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Non-interventional, Prospective, Cross-sectional Study of the Incidence of Pulmonary, Cardiovascular and Renal System Non-communicable Complications Associated With the Post-acute Phase of the Infection by Sars-Cov-2
- ClinicalTrials.gov ID
- NCT06608849
- Acronym / sponsor ID
- POINT / POINT
- Keywords
- Covid-19, SARS-CoV-2, Pulmonary complications, Cardiovascular complications, Renal complications, Post-acute phase, Non communicable diseases, Biomarkers
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 345 participants (estimated)
- Lead sponsor
- Hellenic Institute for the Study of SepsisUniversity, hospital or other
- Study start
- 10 Dec 2024 (actual)
- Primary completion
- 4 Nov 2027 (estimated)
- Study completion
- 4 Nov 2027 (estimated)
- First posted
- 23 Sep 2024 (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.
More than 660 million cases of COVID-19 have been reported worldwide, with 183 million cases in the EU alone. In several people, after recovery, the effects of the first waves of COVID-19 persisted beyond the acute phase and increased the risk of chronic multiorgan symptoms and disease. Up to 70% of people affected by COVID-19 showed reduced organ function even four months or more after COVID-19 diagnosis. Such a functional decline is associated with an increased risk of the development of non-communicable diseases (NCDs). Thus, there is an essential need for a better knowledge, tools, clinical guidelines and recommendations that it will make it possible to reduce this overrepresentation of NCDs as a consequence of the post-acute phase (PAP) of COVID-19.
The overall concept underpinning "POINT" is to i) build detailed knowledge on the link between the PAP of COVID-19 caused by previous, current, and future SARS-CoV-2 variants in vaccinated and unvaccinated people, and NCDs, ii) identify robust biomarkers and build predictive tools that help early identification and management of risk of NCDs, and iii) develop guidelines and recommendations for all parts of the healthcare value chain, allowing best prevention and care acknowledging vulnerability. The investigators will focus on the NCDs affecting pulmonary, cardiovascular and renal systems.
Detailed description
Post-acute phase of COVID and Non-communicable diseases
Following the emergence of SARS-CoV-2, more than 660 million cases of COVID-19 have been reported worldwide, with 183 million cases in the EU alone. These numbers will continue to grow even after the disease becomes endemic. In some people, after recovery, the effects of the first waves of COVID-19 persisted beyond the acute phase and increased the risk of chronic multiorgan symptoms and disease. Up to 70% of people affected by COVID-19 showed reduced organ function even four months or more after COVID-19 diagnosis. Such a functional decline is associated with an increased risk of the development of non-communicable diseases (NCDs). This is especially true for individuals aged 65 and older as the risk of NCDs increases with age.
Diseases of the pulmonary, cardiovascular, and renal systems are the three major NCDs carrying the most significant burden for the individual as well as society. Studies have documented compromised function of these 3 organ systems in the PAP of COVID-19 in 30%-70% of patients, regardless of the severity of the acute-phase. As homeostasis of these three organs depends on interorgan communication with each other, the impact of PAP of COVID-19 on one will impact the others. The added stress of the PAP of COVID-19 increases the risk of a higher incidence and/or the risk of an accelerated progression of disease.
The prevalence and socioeconomic cost of the three NCDs is already extremely high. Without a strong focus on minimmising the increased risk of incidence and accelerated progression of the NCDs as a result of the PAP of COVID-19, up to 9 million Europeans may be affected and result in an added direct attributable cost of between 19.564 € - 31.064 € per year for each person who develop an NCD.
Beyond state of the art: pulmonary, cardiovascular and renal complications after the PAP of COVID-19
Post-acute COVID-19 and pulmonary complications - Respiratory conditions have been reported as occurring twice as often after severe COVID-19 as in the general population. In a study of 135 individuals, the incidence of impaired lung diffusing capacity (DLCO) and persistent lung damage was demonstrated in 30% of patients 12 months after acute COVID-19. In another study of 142 individuals, pulmonary abnormalities were observed by CT scans in 54% of individuals a year after acute COVID-19.
Post-acute COVID-19 and cardiovascular complications - The PAP of COVID-19 is associated with an increased risk of deep vein thrombosis up to three months after COVID-19 infection, pulmonary embolism up to six months, and a bleeding event up to two months. In a registry study of 153,760 individuals with COVID-19, the 12 month period following the acute phase was characterized by an increased risk and an excess disease burden of cardiovascular diseases, including heart failure, dysrhythmias and stroke. The risks were evident regardless of age, race, sex, and other cardiovascular risk factors. MRI revealed cardiac impairment in 78% of 100 individuals in the PAP of COVID-19.
Post-acute COVID-19 and renal complications - A study of 1733 individuals documented reduced renal function in 35% 6 months after the acute phase of COVID-19 and 13% of patients who did not have acute kidney injury (AKI) during the acute phase showed a disproportionate reduction in renal function during follow-up. A study including \>89,000 individuals revealed an increased risk of adverse renal outcomes in the PAP of COVID-19.
The main unmet needs requiring action at the European level There is an urgent need to enable a better understanding of the causality between PAP of COVID-19 and the increased risk of pulmonary, cardiovascular, and renal complications and thereby an increased risk of onset of disease or aggravation of existing disease. Even though recent studies suggest such a link, there is a need for a more nuanced study of the correlation on much larger cohorts to determine the incidence and risk ratio more accurately. Furthermore, there is a need to compare the outcomes between the early, present, and potential future strains of SARS-CoV-2 variants responsible for the disease. An increased cohort size will also allow a better understanding of the impact of socioeconomic status, difference between sexes, the compounding effects of genotype, pre-existing comorbidities, and use of prescription drugs and of differences between the PAP of early strains of SARS-CoV-2 in mostly unvaccinated individuals compared with current strains in mostly vaccinated people. As this knowledge is currently incomplete, there is an immediate risk that a large part of the European population will not receive optimal and timely care.
Thus far, investigators have concluded that the functional decline of organs caused by COVID-19 cannot be explained by known risk factors. A review of the recent literature suggests that the PAP of COVID-19 is associated with immune dysregulation, elevated levels of autoantibodies, microbiota disruption and clotting and endothelial abnormalities. However, the same review also concludes that the current understanding is not sufficient to improve outcomes and calls for additional research. This underscores the involvement of unidentified molecular mechanisms responsible for the aetiology. A lack of understanding of these inhibits the development of effective biomarkers and drug candidates that allow optimal prediction of the prognosis and treatment of patients following resolution of the initial symptoms of COVID-19.
There is an urgent need for updated clinical practice guidelines and new tools to diagnose and prevent the development and aggravation of NCDs caused by the PAP of COVID-19. Currently, there are very few clinical guidelines and recommendations related to the PAP of COVID-19 and NCDs in general, and there are even fewer clinical guidelines and recommendations that focus on the effects of the PAP of COVID-19 on pulmonary, cardiovascular, and renal health. Modern clinical practice guidelines and recommendations that efficiently bridge the gap between research and current practice are invaluable for securing best quality of care, patient outcomes and cost effectiveness. Unfortunately, the development of a guideline or a recommendation does not necessarily lead to changes in clinical practice. Clinical guidelines and recommendations are not always followed, and it is estimated that approximately 30%-40% of patients receive treatment that is not based on scientific evidence and 20%-25% receive treatments that are not needed or potentially harmful.
Study design
- Observational model
- Other
- Time perspective
- Cross-sectional
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Comparators | – | Other: Blood samples, Other: Six-minute walk test, Spirometry, HRCT, Heart ultrasound, Completion of questionnaires of symptomsComparators without medical history of acute infection by SARS-CoV-2. |
| Participants with NO dysfunction | – | Other: Blood samples, Other: Six-minute walk test, Spirometry, HRCT, Heart ultrasound, Completion of questionnaires of symptomsPatients fully recovered by acute COVID-19 who did not present any acute organ injury during acute infection by SARS-CoV-2. |
| Participants with Dysfunctions | – | Other: Blood samples, Other: Six-minute walk test, Spirometry, HRCT, Heart ultrasound, Completion of questionnaires of symptomsPatients who presented signs of lung, heart, and kidney dysfunction during acute infection by SARS-CoV-2. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- POINT will include patients who have participated in the studies ESCAPE, SAVE, SAVE-MORE and SAVE-LONG. For these patients blood samples and clinical data are already available (Baseline - Year 0 from ESCAPE, SAVE \& SAVE-MORE and Year 1 from SAVE-LONG). POINT needs to enroll three groups of patients (selected by the existing biobank mentioned above, based on the inclusion and exclusion study criteria) to cover the magnitude of the spectrum of COVID-19: * Group A (115 Comparators): Comparators without medical history of acute infection by SARS-CoV-2. * Group B (115 with NO dysfunction): Patients fully recovered by acute COVID-19 who did not present any acute organ injury during acute infection by SARS-CoV-2. * Group C (115 with Dysfunctions): Patients who presented signs of lung, heart, and kidney dysfunction during acute infection by SARS-CoV-2.
Key inclusion criteria (12 listed)
- Group A (comparators)
- Adults (18 years or more) of both genders
- Negative history of acute COVID-19
- Group B (patients with ΝΟ dysfunction)
- Adults (18 years or more) of both genders
Key exclusion criteria (19 listed)
- Group A (comparators)
- Any other co-existing disorder generating clinical symptoms
- Failure to thrive according to the attending physicians
- Pregnancy or lactation
- Group B (patients with ΝΟ dysfunction)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Blood samplesBlood sampling for proteomics and transcriptomics, suPAR measurement \& isolation and stimulation of peripheral blood mononuclear cells, eGFR, serum creatinine, cystatin c \& urea | Other | Comparators, Participants with Dysfunctions, Participants with NO dysfunction |
| Six-minute walk test, Spirometry, HRCT, Heart ultrasound, Completion of questionnaires of symptomsSpirometry for forced expiratory volume in the first, second, total lung capacity and diffusion capacity of carbon monoxide. | Other | Comparators, Participants with Dysfunctions, Participants with NO dysfunction |
Primary outcome
The incidence of any organ dysfunction during the first 48 months among patients of group C compared to group B
Time frame: From enrollment to Month 48
This is a composite endpoint which includes the development of chronic failures of at least one of lung, heart and/or kidneys
5 secondary outcomes
The incidence of any organ dysfunction during the first 48 months among patients of group C compared to group A.
Time frame: From enrollment to Month 48.
The incidence of any organ dysfunction during the first 48 months among patients of group B compared to group A.
Time frame: From enrollment to Month 48.
The incidence of chronic lung failure during the first 48 months among patients of group C compared to group B.
Time frame: From enrollment to Month 48.
• The incidence of chronic heart failure during the first 48 months among patients of group C compared to group B.
Time frame: From enrollment to Month 48.
• The incidence of chronic renal disease during the first 48 months among patients of group C compared to group B.
Time frame: From enrollment to Month 48.
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 17 Nov 2025.
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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.
Prof. Evangelos Giamarellos-Bourboulis study chair
Hellenic Institute for the Study of Sepsis
6 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Pulmonary Complications and Cardiovascular Complications, run by Hellenic Institute for the Study of Sepsis at 6 sites in Greece.
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 12 inclusion and 19 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: looking for participants now, as of the sponsor's last update on 17 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 6 sites in Greece. Whether a site is taking part right now should be confirmed with that site. See every site.
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 Prof. Evangelos Giamarellos-Bourboulis (00302105831994, egiamarel@med.uoa.gr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The incidence of any organ dysfunction during the first 48 months among patients of group C compared to group B (time frame: From enrollment to Month 48). 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 17 Nov 2025.