Depression ChronicDaliaMonitorinNCT07211984
Evaluation of Dalia Solution For Depressed Patient
A study testing Dalia Monitoring and Conventional healthcare in people with Depression Chronic and Depressed, run by Dalia Care at 1 site in France.
Trial summary
The goal of this superiority clinical investigation, prospective, multicenter, controlled, randomized, open-label is to evaluate the clinical impact of the Dalia medical telemonitoring device on the management of depressive patients. Read more about this study
- Who is it for?
- Ages 18 to 76 years
- Conditions the study is for
- Depression Chronic, Depressed, Depressed Mood
- What is being tested?
- Dalia Monitoring and Conventional healthcare
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 644 participants
- Where
- 1 siteFrance
- Study dates
- 10 Oct 2025to 31 Mar 2026
- Phase
- Interventional
- 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 to 76 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age ≥ 18 years
- Patient with a diagnosis of depressive episode, as defined by ICD-11, and with a PHQ-9 score ≥ 15 confirmed by a psychiatrist or general practitioner
- Patient receiving a first antidepressant treatment (treatment-naïve) OR having had a modification of antidepressant treatment in the two weeks prior to inclusion
- Patient equipped with a smartphone or a computer or a tablet with internet access
- Patient affiliated to a health insurance scheme
- Patient able to read and understand French
- Patient having signed informed consent
Who cannot join
- Patient under non-cardioselective beta-blocker (carvedilol, labetalol, propranolol, pindolol) and beta-mimetic (salbutamol, terbutaline)
- Patient with a pacemaker or with a known cardiac arrhythmia
- Patient with major neurocognitive disorder (e.g., dementia) or psychotic disorders likely to compromise participation in the study
- Patient hospitalized at the time of inclusion whose discharge is not planned within the next two weeks
- Patient treated with esketamine
- Patient with excessive consumption of psychoactive substances (alcohol or drugs), which may interfere with the course or follow-up of the study
Show all 11Show fewer
- Patient unable to wear the bracelet during the study due to dermatological conditions
- Patient under guardianship, curatorship, or legal protection, or any other administrative or judicial measure depriving rights and freedom
- Patient considered non-autonomous by the investigator
- Patient already included in another interventional research study
- Vulnerable persons referred to in Articles L.1121-5 to 8 and L.1122-1-2 of the French Public Health Code are excluded from the study
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
France1 site
Neurostim Luxembourg
Paris, 75005
Alexis Bourla, paris5@neurostimfrance.com
Stéphane Mouchabac, Pr
About this study
Official title: Evaluation of the Clinical and Organizational Impact of the Digital Medical Device Dalia in the Management of Depression
The goal of this superiority clinical investigation, prospective, multicenter, controlled, randomized, open-label is to evaluate the clinical impact of the Dalia medical telemonitoring device on the management of depressive patients. The main question it aims to answer is: the percentage of patients with clinically significant improvement at 3 months. A clinically significant improvement is defined as a decrease of at least 5 points from the initial PHQ-9 score AND/OR a PHQ-9 score lower than 15. The threshold of 5 points is the Minimal Clinically Important Difference (MCID) of the PHQ-9 scale
Read the detailed description
Worldwide, depression is a disease that affects 3.8% of the population, i.e., about 280 million people [1]. INSERM specifies that major depressive disorder affects all ages of life and concerns about 15 to 20% of the general population [2]. In France, 12.5% of people aged 18-85 years had a history of major depressive episode (MDE) during the past 12 months in 2021 [3]. In 2017, the prevalence of MDE during the past 12 months was 8.2% among the employed French active population [4].
The diagnosis of MDE is clinical. The symptoms of an MDE must persist for at least 2 weeks, and each of them at a certain degree of severity, almost every day. These symptoms must represent a change compared to the patient's usual functioning (professional, social, family) and cause significant distress. Among the main symptoms: depressed mood, loss of interest, dejection, loss of energy, increased fatigability [5]. Standardized assessment tools are diagnostic aids, notably the Patient Health Questionnaire-9 (PHQ-9), the Montgomery-Åsberg Depression Rating Scale (MADRS), the Beck Depression Inventory-II (BDI-II), the Hospital Anxiety and Depression Scale (HADS), and the Hamilton Depression Rating Scale (HDRS) [5].
A first depressive episode may be isolated and resolve spontaneously within six to nine months without specific treatment. However, in most cases, drug treatment is necessary. As a rule, after 8 weeks of a well-conducted drug treatment, one third of patients show complete remission of symptoms, one third show partial remission, and one third do not respond to treatment [2]. One of the main clinical aspects of depression is its recurrent nature. The risk of having another depressive episode gradually increases after each decompensation. Thus, after a first decompensation, more than 50% of individuals will develop a second depressive episode. After two episodes, the relapse rate increases to 70%, and beyond three episodes, to 90% [6].
Due to its consequences at the individual and societal level, depression is a major public health issue, generating high costs related to absenteeism but also to the overall management of affected individuals [7-9]. Indeed, depression impairs the daily functioning, social and professional relationships of affected individuals, and is associated with suicidal behaviors that are very frequent in these individuals. In France, mental health is now a priority, with health insurance expenditures exceeding 23 billion euros in 2023 [8,9]. When including indirect costs, total expenditures related to psychiatric illnesses could exceed 163 billion euros, with depressive and anxiety disorders being among the main causes of years of life lost due to disability [10].
Based on data from the literature, during a major depressive episode, several physical and physiological parameters (heart rate, physical activity, oxygen saturation, and body temperature) are disrupted [13-23]. Continuous monitoring of these parameters would make it possible to better characterize depressive patients and to detect early relapse/recurrence. Early detection of the risk of relapse and recurrence of MDEs could allow for early management.
In France, geographical disparities in the distribution of psychiatrists, with a high concentration in Île-de-France compared to other regions, limit access to care for patients requiring their expertise [22-24]. General practitioners have become the main resource for patients suffering from mental disorders or psychological distress. Indeed, it is estimated that 15 to 40% of the active patient load of general practitioners present a mental disorder or psychological distress [25,26]. However, although trained in the management of somatic pathologies, general practitioners sometimes lack specific skills to recognize, support, and thoroughly treat mental disorders. This often leads to limited management and high prescription of psychotropic drugs. It is estimated that 90% of first-line antidepressant prescriptions come from general practitioners, but follow-up remains insufficient [25,27].
In the literature, digital solutions such as mobile applications have demonstrated their effectiveness in improving mental well-being and reducing symptoms of depression and anxiety [28-31]. Indeed, several systematic reviews and meta-analyses have reported the effectiveness of mHealth interventions based on applications for the management of anxiety and depression symptoms, with effects ranging from small to moderate compared to control groups [32-34]. Medical telemonitoring could play a key role in facilitating this coordination and follow-up of patients by generating alerts adapted to their situation. These data, integrated via dedicated solutions, allow real-time adjustment of the specific management of each patient according to the needs and circumstances generating this alert. However, in France, there is currently no medical telemonitoring device in mental health reimbursed by Health Insurance. Standard follow-up consultations do not always allow continuous monitoring of the patient's condition fluctuations; hence the need for tools enabling early detection of worsening depressive symptoms.
Telemonitoring interventions for depressive patients are generally based on digital tools allowing patients to report their symptoms and health behaviors. This information, called ePROs (electronic Patient-Reported Outcomes), is transmitted to healthcare professionals for continuous monitoring. This approach facilitates the early detection of symptoms, improves communication between patients and caregivers, and allows rapid intervention if necessary. The integration of a telemonitoring solution, Dalia, which continuously collects physiological parameters, offers a considerable advantage compared to a simple collection of ePROs. Indeed, ePROs rely on the patient's subjective reports, which may lead to biases related to the perception or memory of symptoms, and their collection is generally limited to fixed intervals. On the other hand, continuous monitoring of physiological parameters, such as heart rate, oxygen saturation, physical activity, and body temperature, makes it possible to obtain objective and real-time data, thus offering a more complete and accurate picture of the patient's condition. This approach not only allows subtle changes and early signs of worsening to be detected before they are even perceived by the patient, but also to personalize interventions proactively, thus reducing the risks of relapse or hospitalization.
By cross-referencing these physiological data with ePROs, it becomes possible to identify therapeutic needs more quickly and adjust treatment, thereby optimizing depression management and improving long-term outcomes.
We therefore hypothesize that the monitoring of depressive patients through Dalia telemonitoring would improve the response to antidepressant treatment, and reduce the risk of relapse, recurrence, as well as the risk of rehospitalization, emergency room visits, and the number of unscheduled consultations; hence the interest of this clinical investigation evaluating the clinical and organizational impact of the Dalia telemonitoring device.
- Conditions
- Depression Chronic, Depressed, Depressed Mood, Depression and Quality of Life, Depression Diagnosis
- Being tested
- Dalia Monitoring, Conventional healthcare
- Keywords
- Depression, PHQ-9, MADRS, Depressive episode, Anxiety disorder, Antidepressant prescriptions, Smartwatch
- Medical subject headings
- Consciousness Disorders, Depression, Anxiety Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dalia MonitoringDevice
All patients consulting psychiatrists and general practitioners in participating centers, meeting all eligibility criteria and agreeing to participate in the study, will be consecutively selected and randomized into one of the two groups. For iInterventional arm: Patients will benefit from Dalia telemonitoring, in addition to conventional care.
Conventional healthcareOther
All patients consulting psychiatrists and general practitioners in participating centers, meeting all eligibility criteria and agreeing to participate in the study, will be consecutively selected and randomized into one of the two groups. For Control arm: Patients in this group will benefit from the conventional care pathway.
| Study group | Role | What they receive |
|---|---|---|
| Control Group | Active comparator | Patients assigned to the "control" group will follow conventional healthcare. According to french "Haute Autorité de Santé", conventional management includes advice on adopting a healthy lifestyle, psychotherapy with a contracted psychologist, and the prescription of antidepressants if necessary. In this case, regular medical follow-up by the general practitioner or psychiatrist is recommended, particularly at the start of antidepressant treatment (notably after the first and second week). Follow-up consultations to assess treatment response should be performed by the physician between M1 and M2, then at M3, M6, and M12, with a frequency adapted according to the clinical evolution of the patient Receives: Other: Conventional healthcare |
| Interventional Arm | Experimental | Patients assigned to the "intervention" group will benefit from Dalia telemonitoring in addition to conventional management. Receives: Device: Dalia Monitoring |
What is being measured
The primary outcome is the main question the study is designed to answer.
Primary Endpoint
The primary endpoint will be the percentage of patients with clinically significant improvement at 3 months.
A clinically significant improvement is defined as a decrease of at least 5 points from the initial PHQ-9 score AND/OR a PHQ-9 score lower than 15.
The threshold of 5 points is the Minimal Clinically Important Difference (MCID) of the PHQ-9 scale
Measured: 12 months after inclusion
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Oct 2025
- Study start10 Oct 2025 (estimated)
- Primary completion31 Mar 2026 (estimated)
- Study completion31 Mar 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Depression ChronicStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 644 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Dalia Care
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Stéphane Mouchabac, Doctor, Principal investigator, Dalia Care
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07211984
- Sponsor's protocol ID
- 2025-A01266-43
- Acronym
- DaliaMonitorin
- Status last verified
- Oct 2025
- First submitted
- 1 Oct 2025
- Last updated
- 8 Oct 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 8 Oct 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of the Clinical and Organizational Impact of the Digital Medical Device Dalia in the Management of Depression
- ClinicalTrials.gov ID
- NCT07211984
- Acronym / sponsor ID
- DaliaMonitorin / 2025-A01266-43
- Conditions
- Depression Chronic, Depressed, Depressed Mood, Depression and Quality of Life, Depression Diagnosis
- Keywords
- Depression, PHQ-9, MADRS, Depressive episode, Anxiety disorder, Antidepressant prescriptions, Smartwatch
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 644 participants (estimated)
- Lead sponsor
- Dalia CareIndustry (pharma, biotech, devices)
- Study start
- 10 Oct 2025 (estimated)
- Primary completion
- 31 Mar 2026 (estimated)
- Study completion
- 31 Mar 2026 (estimated)
- First posted
- 8 Oct 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.
The goal of this superiority clinical investigation, prospective, multicenter, controlled, randomized, open-label is to evaluate the clinical impact of the Dalia medical telemonitoring device on the management of depressive patients. The main question it aims to answer is: the percentage of patients with clinically significant improvement at 3 months. A clinically significant improvement is defined as a decrease of at least 5 points from the initial PHQ-9 score AND/OR a PHQ-9 score lower than 15. The threshold of 5 points is the Minimal Clinically Important Difference (MCID) of the PHQ-9 scale
Detailed description
Worldwide, depression is a disease that affects 3.8% of the population, i.e., about 280 million people [1]. INSERM specifies that major depressive disorder affects all ages of life and concerns about 15 to 20% of the general population [2]. In France, 12.5% of people aged 18-85 years had a history of major depressive episode (MDE) during the past 12 months in 2021 [3]. In 2017, the prevalence of MDE during the past 12 months was 8.2% among the employed French active population [4].
The diagnosis of MDE is clinical. The symptoms of an MDE must persist for at least 2 weeks, and each of them at a certain degree of severity, almost every day. These symptoms must represent a change compared to the patient's usual functioning (professional, social, family) and cause significant distress. Among the main symptoms: depressed mood, loss of interest, dejection, loss of energy, increased fatigability [5]. Standardized assessment tools are diagnostic aids, notably the Patient Health Questionnaire-9 (PHQ-9), the Montgomery-Åsberg Depression Rating Scale (MADRS), the Beck Depression Inventory-II (BDI-II), the Hospital Anxiety and Depression Scale (HADS), and the Hamilton Depression Rating Scale (HDRS) [5].
A first depressive episode may be isolated and resolve spontaneously within six to nine months without specific treatment. However, in most cases, drug treatment is necessary. As a rule, after 8 weeks of a well-conducted drug treatment, one third of patients show complete remission of symptoms, one third show partial remission, and one third do not respond to treatment [2]. One of the main clinical aspects of depression is its recurrent nature. The risk of having another depressive episode gradually increases after each decompensation. Thus, after a first decompensation, more than 50% of individuals will develop a second depressive episode. After two episodes, the relapse rate increases to 70%, and beyond three episodes, to 90% [6].
Due to its consequences at the individual and societal level, depression is a major public health issue, generating high costs related to absenteeism but also to the overall management of affected individuals [7-9]. Indeed, depression impairs the daily functioning, social and professional relationships of affected individuals, and is associated with suicidal behaviors that are very frequent in these individuals. In France, mental health is now a priority, with health insurance expenditures exceeding 23 billion euros in 2023 [8,9]. When including indirect costs, total expenditures related to psychiatric illnesses could exceed 163 billion euros, with depressive and anxiety disorders being among the main causes of years of life lost due to disability [10].
Based on data from the literature, during a major depressive episode, several physical and physiological parameters (heart rate, physical activity, oxygen saturation, and body temperature) are disrupted [13-23]. Continuous monitoring of these parameters would make it possible to better characterize depressive patients and to detect early relapse/recurrence. Early detection of the risk of relapse and recurrence of MDEs could allow for early management.
In France, geographical disparities in the distribution of psychiatrists, with a high concentration in Île-de-France compared to other regions, limit access to care for patients requiring their expertise [22-24]. General practitioners have become the main resource for patients suffering from mental disorders or psychological distress. Indeed, it is estimated that 15 to 40% of the active patient load of general practitioners present a mental disorder or psychological distress [25,26]. However, although trained in the management of somatic pathologies, general practitioners sometimes lack specific skills to recognize, support, and thoroughly treat mental disorders. This often leads to limited management and high prescription of psychotropic drugs. It is estimated that 90% of first-line antidepressant prescriptions come from general practitioners, but follow-up remains insufficient [25,27].
In the literature, digital solutions such as mobile applications have demonstrated their effectiveness in improving mental well-being and reducing symptoms of depression and anxiety [28-31]. Indeed, several systematic reviews and meta-analyses have reported the effectiveness of mHealth interventions based on applications for the management of anxiety and depression symptoms, with effects ranging from small to moderate compared to control groups [32-34]. Medical telemonitoring could play a key role in facilitating this coordination and follow-up of patients by generating alerts adapted to their situation. These data, integrated via dedicated solutions, allow real-time adjustment of the specific management of each patient according to the needs and circumstances generating this alert. However, in France, there is currently no medical telemonitoring device in mental health reimbursed by Health Insurance. Standard follow-up consultations do not always allow continuous monitoring of the patient's condition fluctuations; hence the need for tools enabling early detection of worsening depressive symptoms.
Telemonitoring interventions for depressive patients are generally based on digital tools allowing patients to report their symptoms and health behaviors. This information, called ePROs (electronic Patient-Reported Outcomes), is transmitted to healthcare professionals for continuous monitoring. This approach facilitates the early detection of symptoms, improves communication between patients and caregivers, and allows rapid intervention if necessary. The integration of a telemonitoring solution, Dalia, which continuously collects physiological parameters, offers a considerable advantage compared to a simple collection of ePROs. Indeed, ePROs rely on the patient's subjective reports, which may lead to biases related to the perception or memory of symptoms, and their collection is generally limited to fixed intervals. On the other hand, continuous monitoring of physiological parameters, such as heart rate, oxygen saturation, physical activity, and body temperature, makes it possible to obtain objective and real-time data, thus offering a more complete and accurate picture of the patient's condition. This approach not only allows subtle changes and early signs of worsening to be detected before they are even perceived by the patient, but also to personalize interventions proactively, thus reducing the risks of relapse or hospitalization.
By cross-referencing these physiological data with ePROs, it becomes possible to identify therapeutic needs more quickly and adjust treatment, thereby optimizing depression management and improving long-term outcomes.
We therefore hypothesize that the monitoring of depressive patients through Dalia telemonitoring would improve the response to antidepressant treatment, and reduce the risk of relapse, recurrence, as well as the risk of rehospitalization, emergency room visits, and the number of unscheduled consultations; hence the interest of this clinical investigation evaluating the clinical and organizational impact of the Dalia telemonitoring device.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control Group | Active comparator | Other: Conventional healthcarePatients assigned to the "control" group will follow conventional healthcare. According to french "Haute Autorité de Santé", conventional management includes advice on adopting a healthy lifestyle, psychotherapy with a contracted psychologist, and the prescription of antidepressants if necessary. In this case, regular medical follow-up by the general practitioner or psychiatrist is recommended, particularly at the start of antidepressant treatment (notably after the first and second week). Follow-up consultations to assess treatment response should be performed by the physician between M1 and M2, then at M3, M6, and M12, with a frequency adapted according to the clinical evolution of the patient |
| Interventional Arm | Experimental | Device: Dalia MonitoringPatients assigned to the "intervention" group will benefit from Dalia telemonitoring in addition to conventional management. |
Who may qualify
- Ages
- 18 to 76 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- Age ≥ 18 years
- Patient with a diagnosis of depressive episode, as defined by ICD-11, and with a PHQ-9 score ≥ 15 confirmed by a psychiatrist or general practitioner
- Patient receiving a first antidepressant treatment (treatment-naïve) OR having had a modification of antidepressant treatment in the two weeks prior to inclusion
- Patient equipped with a smartphone or a computer or a tablet with internet access
- Patient affiliated to a health insurance scheme
Key exclusion criteria (11 listed)
- Patient under non-cardioselective beta-blocker (carvedilol, labetalol, propranolol, pindolol) and beta-mimetic (salbutamol, terbutaline)
- Patient with a pacemaker or with a known cardiac arrhythmia
- Patient with major neurocognitive disorder (e.g., dementia) or psychotic disorders likely to compromise participation in the study
- Patient hospitalized at the time of inclusion whose discharge is not planned within the next two weeks
- Patient treated with esketamine
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 |
|---|---|---|
| Dalia MonitoringAll patients consulting psychiatrists and general practitioners in participating centers, meeting all eligibility criteria and agreeing to participate in the study, will be consecutively selected and randomized into one of the two groups. For iInterventional arm: Patients will benefit from Dalia telemonitoring, in addition to conventional care. | Device | Interventional Arm |
| Conventional healthcareAll patients consulting psychiatrists and general practitioners in participating centers, meeting all eligibility criteria and agreeing to participate in the study, will be consecutively selected and randomized into one of the two groups. For Control arm: Patients in this group will benefit from the conventional care pathway. | Other | Control Group |
Primary outcome
Primary Endpoint
Time frame: 12 months after inclusion
The primary endpoint will be the percentage of patients with clinically significant improvement at 3 months. A clinically significant improvement is defined as a decrease of at least 5 points from the initial PHQ-9 score AND/OR a PHQ-9 score lower than 15. The threshold of 5 points is the Minimal Clinically Important Difference (MCID) of the PHQ-9 scale
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 8 Oct 2025.
- Sponsor WebsiteLink provided by the sponsor.
- Individual participant dataSharing planned: Undecided
Related trials for Depression Chronic
Recruiting
Marine Lipids Ease Painful TMD
Temporomandibular Disorder (TMD)
Recruiting
Application of Meaning-Based Psychotherapy to a Sample of Patients With Chronic Pain
Chronic Pain
Recruiting
Virtual Reality-Based Hypnotherapy for Pain, Sleep, and Mood in Spinal Cord Injury
Spinal Cord Injuries (SCI), Chronic Pain
Not yet recruiting
Transcranial Direct Current Stimulation for Chemotherapy-Related Chronic Pain in Cancer Survivors
Chronic Pain, Neuropathic Pain
Active, not recruiting
Acceptance and Commitment Therapy-Based Group Psychotherapy for Chronic Headache
Chronic Headache
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.
Stéphane Mouchabac, Doctor principal investigator
Dalia Care
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Dalia Monitoring and Conventional healthcare in people with Depression Chronic and Depressed, run by Dalia Care at 1 site in France.
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 7 inclusion and 11 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 8 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. 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 Nour Hakiki Belhadi (+33758082693, nour@daliacare.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Primary Endpoint (time frame: 12 months after inclusion). 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 8 Oct 2025.