Hepatitis CPhase 4CICHepCNCT02745132
Cognitive Impairments in Chronic Hepatitis C Patients and Potential Reversibility With New Agents (CICHepC)
A Phase 4 study testing Neuropsychological evaluation and Brain MRI in people with Hepatitis C, run by Instituto de Investigación Marqués de Valdecilla at 1 site in Spain.
Trial summary
The overall aim of this study is to evaluate the prevalence of cognitive impairments and brain anomalies in Chronic Hepatitis C infected individuals and to investigate likely changes in cognition and brain structure and function after treatment with Direct-acting Antivirals (DAAs). Read more about this study
- Who is it for?
- Ages 18 to 75 years
- Conditions the study is for
- Hepatitis C
- What is being tested?
- Neuropsychological evaluation and Brain MRI
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteSpain
- Study dates
- Jun 2016to Dec 2017
- Phase
- Phase 4
- Are there results?
- None posted in the registry
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 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- CHC patients 18-75 years old
- Liver fibrosis ≤ F3 in Fibroscan/liver biopsy
- Naive or previous failure to a treatment
- Accept the study and sign the CI
Who cannot join
- Does not meet the above criteria
- VIH or other viral coinfection
- Hepatocarcinoma
- Other systemic inflammatory diseases (i.e. RA, etc)
- Neurodegenerative diseases
Trial locations and contacts
1 site in 1 country.
Spain1 site
Hospital Universitario Marqués de Valdecilla
Santander, Cantabria, 39008
Javier Crespo García, MDPhD, 34 942202544, javiercrespo1991@gmail.com
Benedicto Crespo Facorro, MDPhD, 34 942202520, bcfacorro@humv.es
About this study
Official title: Personalized Medicine in HCV Infection: Cognitive Impairments and Brain Anomalies in Chronic Hepatitis C Infected Individuals. Characterization and Potential Reversibility With Direct Antiviral Agents.
The overall aim of this study is to evaluate the prevalence of cognitive impairments and brain anomalies in Chronic Hepatitis C infected individuals and to investigate likely changes in cognition and brain structure and function after treatment with Direct-acting Antivirals (DAAs).
Read the detailed description
Design: Prospective interventional study.
Chronic HCV infected patients who are going to initiate a DAA-based antiviral regimen according to clinical practice will be recruited to participate in the study. Patients will be treated according to the current national and international guidelines for the treatment of HCV chronic hepatitis. The participation in the study will not influence neither the indication for de treatment nor the type of treatment prescribed. The only intervention in this study refers to the performance of extraordinary neuro-psychological evaluations and MRI studies at different times along the study.
Patients and methods:
This study will be performed in a cohort of 80 patients with CHC (≤ F3). The number of subjects required to test effects with sufficient power over the entire cortex varies between cortical measures (cortical thickness: N=39, surface area: N=21, volume: N=81; 10mm smoothing, power=0.8, α =0.05). For subcortical regions this number is between 16 and 76 subjects, depending on the region (Liem et al., 2015). Sample size calculations performed for functional magnetic resonance using values of medium Cohen's d effect size of 0.6 and 0.7 yield sample sizes of 88, 66 respectively to achieve 80% power at a significance level of 0.05 (Guo et al., 2012). Therefore, the sample size estimated in this project would yield enough power to detect small and medium effects size.
The following studies will be conducted:
- - Cognitive assessment: The assessment with widely-used neuropsychological test batteries may yield summary scores for the domains: attention and reaction time (Continuous Performance Test (CPT), working memory (digits forward and backward WAIS-III subtest), information processing speed (digit symbol WAIS-III subtest and Trail making test Part A), verbal fluency (letter FAS and category animals subtest), learning and memory (Rey Auditory 2.- Verbal Learning Test (RAVLT) and Rey Copy Figure(RCF)), motor functioning (Grooved Pegboard) and executive functions (Tower of London, Trail making test Part B and Stroop color-word test).
- - MRI scanning: Imaging data will be acquired at the neurorradiology section of the Hospital Marques de Valdecilla, on a 3T MRI scanner (Achieva, Philips Medical Systems, Best, The Netherlands) at the Neuroradiology Department of "Marques de Valdecilla" University Hospital. Subjects will undergo a 30 minutes protocol that will include a high resolution T1- weighted image, a 64 directions DWI sequence and A BOLD resting state fMRI sequence.
- - MRI data analysis: It will involve structural, diffusion and functional MRI analyses. These analyses will be conducted by Neuroimaging Platform at the IDIVAL.
3.1.- Structural MRI: we will use the software FreeSurfer (http://freesurfer.net/) to quantify the volume of subcortical structures (amygdala, hippocampus, thalamus, putamen, globus pallidus, and caudate nucleus) and the area, thickness, and volume of 34 cortical structures (Desikan-Killiany atlas).
3.2.- Diffusion MRI: we will use FSL's TBSS and Probtracx tools http://www.fmrib.ox.ac.uk/fsl/index.html) to compare fractional anisotropy values (a measure based on restricted movement of water molecules) in whole brain voxelwise analysis and identify regions (clusters) where white matter is more disorganized.
Also we will perform fiber tracking and study connectivity between different brain areas.
3.3.- Functional MRI (fMRI): resting state fmri will be used to evaluate regional interactions that occur when non performing and specific task. This analysis will be carried out with using SPM software http://www.fil.ion.ucl.ac.uk/spm/) and the toolbox PRONTO (http://www.mlnl.cs.ucl.ac.uk/pronto ).
- Conditions
- Hepatitis C
- Being tested
- Neuropsychological evaluation and Brain MRI
- Keywords
- Chronic, Cognition Disorders, Neurocognition Disorders, Cognitive Impairments, Diffusion Magnetic Resonance Imaging, MRI functional, Verbal fluency
- Medical subject headings
- Hepatitis C, Bronchiolitis Obliterans Syndrome, Cognition Disorders, Cognitive Dysfunction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Neuropsychological evaluation and Brain MRIOther
This is a prospective study. The only intervention planned will consist of performing neuropsychological tests and cerebral MRI that will be carried out on a single group cohort at different times.
Notwithstanding, we will record the exposure to DAA to assess any change in neurocognitive function and MRI imaging.
Anti-HCV regimens will be used according to clinical practice as indicated into the current guidelines (1)
(1)European Association for Study of Liver. EASL Recommendations on Treatment of Hepatitis C 2015. J Hepatol. 2015 Jul;63(1):199-236. doi: 10.1016/j.jhep.2015.03.025. Epub 2015 Apr 21. PubMed PMID: 25911336.
| Study group | Role | What they receive |
|---|---|---|
| Cognitive evaluation in HCV patients | Other | Neuropsychological evaluation and Brain MRI
Intervention: The only intervention to be carried out along the study will consist of complete neuro-psychological tests and MRI studies performed at different times.
Chronic HCV patients who are going to be treated with new DAAs according to current guidelines will be studied: A neuro-psychological battery of tests and brain MRI studies will be performed at different times before and after the end of the treatment. The participation in the study will not influence neither the indication to treat nor the treatment used.
Anti-HCV regimens will be used according to clinical practice as indicated into the current guidelines Receives: Other: Neuropsychological evaluation and Brain MRI |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in Continuous Performance Test (CPT) score
Neuropsychological test to assess Cognitive impairment, particularly Attention and reaction time
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Secondary outcomes (15)
Changes in Digits forward and backward WAIS-III subtest scores
Neuropsychological test to assess Cognitive impairment, particularly Working memory
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Digit symbol WAIS-III subtest score
Neuropsychological test to assess Information processing speed
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Trail Making Test (TMT) Parts A & B scores
Neuropsychological test to assess Information processing speed
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Letter FAS score
Neuropsychological test to assess Verbal fluency
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in animal category subtest score
Neuropsychological test to assess Verbal fluency
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Rey Auditory Verbal Learning Test (RAVLT) scores
Neuropsychological test to assess Learning and memory
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Rey Copy Figure(RCF) scores
Neuropsychological test to assess Learning and memory
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Grooved Pegboard score
Neuropsychological test to assess Motor functioning
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Tower of London score
Neuropsychological test to assess Executive functions
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Stroop color-word test scores
Neuropsychological test to assess Executive functions
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in cortical thickness
Basal Neuroimaging findings in HCV infected patients and changes after DAA treatment (Assesed through structural, diffusion and functional MRI).
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in cortical surface área assessed by MRI
Basal Neuroimaging findings in HCV infected patients and changes after DAA treatment (Assesed through structural, diffusion and functional MRI).
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in cortical surface volumen assessed by MRI
Basal Neuroimaging findings in HCV infected patients and changes after DAA treatment (Assesed through structural, diffusion and functional MRI).
Measured: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Sustained Viral Response
Data on efficacy of treatments
Measured: 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Advers events
Data on safety
Measured: up to 24 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Apr 2016 (estimated)
- Study startJun 2016
- Primary completionDec 2017 (estimated)
- Study completionDec 2017 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Hepatitis CStudies 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 4
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Instituto de Investigación Marqués de Valdecilla
- Sponsor type
- University, hospital or other
- Collaborators
- Ministerio de Economía y Competitividad, Spain
- Responsible party
- Sponsor
- Investigators
- Javier Crespo García, MDPhD, Principal investigator, Head of Gastroenterology and Hepatology at Hospital Universitario Marqués de Valdecilla. Professor at the Universidad de CantabriaBenedicto Crespo Facorro, MDPhD, Principal investigator, Head of section Of Psychiatry at University Hospital Marqués de Valdecilla. Proffesor of Psychiatry at Department of Psychiatry, School of Medicine
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02745132
- Sponsor's protocol ID
- CICHepC-PIE15/00079-JCG
- Other IDs
- PIE15/00079
- Acronym
- CICHepC
- Status last verified
- Apr 2016
- First submitted
- 10 Apr 2016
- Last updated
- 21 Apr 2016
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Publications
Byrnes V, Miller A, Lowry D, Hill E, Weinstein C, Alsop D, Lenkinski R, Afdhal NH. Effects of anti-viral therapy and HCV clearance on cerebral metabolism and cognition. J Hepatol. 2012 Mar;56(3):549-56. doi: 10.1016/j.jhep.2011.09.015. Epub 2011 Oct 23.
PubMed 22027578Fletcher NF, Wilson GK, Murray J, Hu K, Lewis A, Reynolds GM, Stamataki Z, Meredith LW, Rowe IA, Luo G, Lopez-Ramirez MA, Baumert TF, Weksler B, Couraud PO, Kim KS, Romero IA, Jopling C, Morgello S, Balfe P, McKeating JA. Hepatitis C virus infects the endothelial cells of the blood-brain barrier. Gastroenterology. 2012 Mar;142(3):634-643.e6. doi: 10.1053/j.gastro.2011.11.028. Epub 2011 Dec 1.
PubMed 22138189Kraus MR, Schafer A, Teuber G, Porst H, Sprinzl K, Wollschlager S, Keicher C, Scheurlen M. Improvement of neurocognitive function in responders to an antiviral therapy for chronic hepatitis C. Hepatology. 2013 Aug;58(2):497-504. doi: 10.1002/hep.26229. Epub 2013 Jun 24.
PubMed 23300053Bajaj JS, Forton DM. Cognitive improvement after HCV eradication: Extending the benefits. Hepatology. 2013 Aug;58(2):480-2. doi: 10.1002/hep.26481. Epub 2013 Jun 25. No abstract available.
PubMed 23696270
Study at a glance
From the registry record, last updated by the sponsor on 21 Apr 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Personalized Medicine in HCV Infection: Cognitive Impairments and Brain Anomalies in Chronic Hepatitis C Infected Individuals. Characterization and Potential Reversibility With Direct Antiviral Agents.
- ClinicalTrials.gov ID
- NCT02745132
- Acronym / sponsor ID
- CICHepC / CICHepC-PIE15/00079-JCG
- Conditions
- Hepatitis C
- Keywords
- Chronic, Cognition Disorders, Neurocognition Disorders, Cognitive Impairments, Diffusion Magnetic Resonance Imaging, MRI functional, Verbal fluency
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- Instituto de Investigación Marqués de ValdecillaUniversity, hospital or other
- Collaborators
- Ministerio de Economía y Competitividad, Spain
- Study start
- Jun 2016
- Primary completion
- Dec 2017 (estimated)
- Study completion
- Dec 2017 (estimated)
- First posted
- 20 Apr 2016 (estimated)
- 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 overall aim of this study is to evaluate the prevalence of cognitive impairments and brain anomalies in Chronic Hepatitis C infected individuals and to investigate likely changes in cognition and brain structure and function after treatment with Direct-acting Antivirals (DAAs).
Detailed description
Design: Prospective interventional study.
Chronic HCV infected patients who are going to initiate a DAA-based antiviral regimen according to clinical practice will be recruited to participate in the study. Patients will be treated according to the current national and international guidelines for the treatment of HCV chronic hepatitis. The participation in the study will not influence neither the indication for de treatment nor the type of treatment prescribed. The only intervention in this study refers to the performance of extraordinary neuro-psychological evaluations and MRI studies at different times along the study.
Patients and methods:
This study will be performed in a cohort of 80 patients with CHC (≤ F3). The number of subjects required to test effects with sufficient power over the entire cortex varies between cortical measures (cortical thickness: N=39, surface area: N=21, volume: N=81; 10mm smoothing, power=0.8, α =0.05). For subcortical regions this number is between 16 and 76 subjects, depending on the region (Liem et al., 2015). Sample size calculations performed for functional magnetic resonance using values of medium Cohen's d effect size of 0.6 and 0.7 yield sample sizes of 88, 66 respectively to achieve 80% power at a significance level of 0.05 (Guo et al., 2012). Therefore, the sample size estimated in this project would yield enough power to detect small and medium effects size.
The following studies will be conducted:
- - Cognitive assessment: The assessment with widely-used neuropsychological test batteries may yield summary scores for the domains: attention and reaction time (Continuous Performance Test (CPT), working memory (digits forward and backward WAIS-III subtest), information processing speed (digit symbol WAIS-III subtest and Trail making test Part A), verbal fluency (letter FAS and category animals subtest), learning and memory (Rey Auditory 2.- Verbal Learning Test (RAVLT) and Rey Copy Figure(RCF)), motor functioning (Grooved Pegboard) and executive functions (Tower of London, Trail making test Part B and Stroop color-word test).
- - MRI scanning: Imaging data will be acquired at the neurorradiology section of the Hospital Marques de Valdecilla, on a 3T MRI scanner (Achieva, Philips Medical Systems, Best, The Netherlands) at the Neuroradiology Department of "Marques de Valdecilla" University Hospital. Subjects will undergo a 30 minutes protocol that will include a high resolution T1- weighted image, a 64 directions DWI sequence and A BOLD resting state fMRI sequence.
- - MRI data analysis: It will involve structural, diffusion and functional MRI analyses. These analyses will be conducted by Neuroimaging Platform at the IDIVAL.
3.1.- Structural MRI: we will use the software FreeSurfer (http://freesurfer.net/) to quantify the volume of subcortical structures (amygdala, hippocampus, thalamus, putamen, globus pallidus, and caudate nucleus) and the area, thickness, and volume of 34 cortical structures (Desikan-Killiany atlas).
3.2.- Diffusion MRI: we will use FSL's TBSS and Probtracx tools http://www.fmrib.ox.ac.uk/fsl/index.html) to compare fractional anisotropy values (a measure based on restricted movement of water molecules) in whole brain voxelwise analysis and identify regions (clusters) where white matter is more disorganized.
Also we will perform fiber tracking and study connectivity between different brain areas.
3.3.- Functional MRI (fMRI): resting state fmri will be used to evaluate regional interactions that occur when non performing and specific task. This analysis will be carried out with using SPM software http://www.fil.ion.ucl.ac.uk/spm/) and the toolbox PRONTO (http://www.mlnl.cs.ucl.ac.uk/pronto ).
Study design
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Cognitive evaluation in HCV patients | Other | Other: Neuropsychological evaluation and Brain MRINeuropsychological evaluation and Brain MRI Intervention: The only intervention to be carried out along the study will consist of complete neuro-psychological tests and MRI studies performed at different times. Chronic HCV patients who are going to be treated with new DAAs according to current guidelines will be studied: A neuro-psychological battery of tests and brain MRI studies will be performed at different times before and after the end of the treatment. The participation in the study will not influence neither the indication to treat nor the treatment used. Anti-HCV regimens will be used according to clinical practice as indicated into the current guidelines |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- CHC patients 18-75 years old
- Liver fibrosis ≤ F3 in Fibroscan/liver biopsy
- Naive or previous failure to a treatment
- Accept the study and sign the CI
Key exclusion criteria (5 listed)
- Does not meet the above criteria
- VIH or other viral coinfection
- Hepatocarcinoma
- Other systemic inflammatory diseases (i.e. RA, etc)
- Neurodegenerative diseases
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 |
|---|---|---|
| Neuropsychological evaluation and Brain MRIThis is a prospective study. The only intervention planned will consist of performing neuropsychological tests and cerebral MRI that will be carried out on a single group cohort at different times. Notwithstanding, we will record the exposure to DAA to assess any change in neurocognitive function and MRI imaging. Anti-HCV regimens will be used according to clinical practice as indicated into the current guidelines (1) (1)European Association for Study of Liver. EASL Recommendations on Treatment of Hepatitis C 2015. J Hepatol. 2015 Jul;63(1):199-236. doi: 10.1016/j.jhep.2015.03.025. Epub 2015 Apr 21. PubMed PMID: 25911336. | Other | Cognitive evaluation in HCV patients |
Primary outcome
Changes in Continuous Performance Test (CPT) score
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Neuropsychological test to assess Cognitive impairment, particularly Attention and reaction time
15 secondary outcomes
Changes in Digits forward and backward WAIS-III subtest scores
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Digit symbol WAIS-III subtest score
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Trail Making Test (TMT) Parts A & B scores
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Letter FAS score
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in animal category subtest score
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Rey Auditory Verbal Learning Test (RAVLT) scores
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Rey Copy Figure(RCF) scores
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Grooved Pegboard score
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Tower of London score
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in Stroop color-word test scores
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in cortical thickness
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in cortical surface área assessed by MRI
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Changes in cortical surface volumen assessed by MRI
Time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Sustained Viral Response
Time frame: 3, 6 and 12 months after the end of treatment (Sustained Viral Response)
Advers events
Time frame: up to 24 weeks
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Apr 2016.
- Background: PubMed 22027578Byrnes V, Miller A, Lowry D, Hill E, Weinstein C, Alsop D, Lenkinski R, Afdhal NH. Effects of anti-viral therapy and HCV clearance on cerebral metabolism and cognition. J Hepatol. 2012 Mar;56(3):549-56. doi: 10.1016/j.jhep.2011.09.015. Epub 2011 Oct 23.
- Background: PubMed 22138189Fletcher NF, Wilson GK, Murray J, Hu K, Lewis A, Reynolds GM, Stamataki Z, Meredith LW, Rowe IA, Luo G, Lopez-Ramirez MA, Baumert TF, Weksler B, Couraud PO, Kim KS, Romero IA, Jopling C, Morgello S, Balfe P, McKeating JA. Hepatitis C virus infects the endothelial cells of the blood-brain barrier. Gastroenterology. 2012 Mar;142(3):634-643.e6. doi: 10.1053/j.gastro.2011.11.028. Epub 2011 Dec 1.
- Background: PubMed 23300053Kraus MR, Schafer A, Teuber G, Porst H, Sprinzl K, Wollschlager S, Keicher C, Scheurlen M. Improvement of neurocognitive function in responders to an antiviral therapy for chronic hepatitis C. Hepatology. 2013 Aug;58(2):497-504. doi: 10.1002/hep.26229. Epub 2013 Jun 24.
- Background: PubMed 23696270Bajaj JS, Forton DM. Cognitive improvement after HCV eradication: Extending the benefits. Hepatology. 2013 Aug;58(2):480-2. doi: 10.1002/hep.26481. Epub 2013 Jun 25. No abstract available.
- Individual participant dataSharing planned: No
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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. This study is not recruiting at the moment.
Javier Crespo García, MDPhD principal investigator
Head of Gastroenterology and Hepatology at Hospital Universitario Marqués de Valdecilla. Professor at the Universidad de Cantabria
Benedicto Crespo Facorro, MDPhD principal investigator
Head of section Of Psychiatry at University Hospital Marqués de Valdecilla. Proffesor of Psychiatry at Department of Psychiatry, School of Medicine
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Neuropsychological evaluation and Brain MRI in people with Hepatitis C, run by Instituto de Investigación Marqués de Valdecilla at 1 site in Spain.
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 4 inclusion and 5 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: status not confirmed, as of the sponsor's last update on 21 Apr 2016. 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 Spain. 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.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Javier Crespo García, MDPhD (34 942 202544, javiercrespo1991@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in Continuous Performance Test (CPT) score (time frame: Basal and 3, 6 and 12 months after the end of treatment (Sustained Viral Response)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02745132, which also lists 4 linked publications.
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 21 Apr 2016.