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AzTrials

Chronic Hepatitis COPALENCT02618928

The Effectiveness of Paritaprevir/Ritonavir - Ombitasvir, ± Dasabuvir, ± Ribavirin in France

An observational study of Chronic Hepatitis C, run by AbbVie at 70 sites in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This study seeks to determine the effectiveness of the interferon-free ABBVIE REGIMEN ± ribavirin (RBV) in participants with chronic hepatitis C (CHC) virus in clinical practices across France. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Chronic Hepatitis C
How many people
735 participants
Where
70 sitesFrance
Study dates
15 Dec 2015to 29 Mar 2018
Phase
Observational
Are there results?
Yes, posted in the registrySummary in the doctors' view

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
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients chronically infected with HCV, receiving the interferon-free ABBVIE REGIMEN, were offered the opportunity to participate in this study during a routine clinical visit at the participating sites.

Who may be able to join

  • Treatment-naïve or -experienced participants with confirmed CHC, genotype 1 or 4
  • Participants receiving or who will receive the interferon-free ABBVIE REGIMEN ± RBV according to product label
  • RBV prescribed in line with the current local label

Who cannot join

  • Participant is not participating or intending to participate in a concurrent interventional therapeutic trial

Trial locations and contacts

70 sites in 1 country.

70 sites in 1 country

France70 sites
  • C.H. du Pays d'Aix /ID# 144922

    Aix-en-Provence, 13090

  • Cabinet medical /ID# 147359

    Aix-en-Provence, 13100

  • CHU Amiens Picardie /ID# 145871

    Amiens, Somme, 80054

  • CHU d'Angers /ID# 145880

    Angers, 49933

  • Centre Hospitalier Victor Dupo /ID# 147241

    Argenteuil, 95107

  • Centre Hospitalier D'Avignon /ID# 151098

    Avignon, 84000

  • Centre Hospitalier D'Avignon /ID# 151343

    Avignon, 84000

  • CHU de Besancon - Jean Minjoz /ID# 145884

    Besançon, Doubs, 25000

  • Cabinet Medical /ID# 147322

    Besançon, 25000

  • Centre Endo Nord Isere /ID# 148694

    Bourgoin, 38300

  • Centre Hospitalier Universitai /ID# 147568

    Caen, 14033

  • CH de Chambery /ID# 145573

    Chambéry, 7301

  • Hopital Antoine Beclere /ID# 149251

    Clamart, 92140

  • Hopital Antoine Beclere /ID# 149252

    Clamart, 92140

  • Hopital Beaujon /ID# 147923

    Clichy, Île-de-France Region, 92110

  • Centre Hosp Intercommunal /ID# 145876

    Créteil, 94010

  • Hospital Henri Mondor /ID# 144918

    Créteil, 94010

  • Clinique du Palais /ID# 145563

    Grasse, 06130

  • CHU de Grenoble - Albet Michal /ID# 145881

    Grenoble, 38043

  • CH d'Hyeres /ID# 145870

    Hyères, 83407

  • Ch Du Mans /Id# 147415

    Le Mans, 72037

  • Dr. Cuissard, Le Port, FR /ID# 145565

    Le Port, 97420

  • Centre Hospitalier de Libourne /ID# 145564

    Libourne, 33500

  • CHU Dupuytren /ID# 144920

    Limoges, Franche-Comte, 87042

  • CH Des Deux Vallees Longumeau /ID# 149336

    Longjumeau, 91161

  • Hopital de la Croix Rousse /ID# 149776

    Lyon, 69004

  • Ctr Consultations La Sauvegard /ID# 147236

    Lyon, 69338

  • Hopital Saint Joseph /ID# 144927

    Marseille, Bouches-du-Rhone, 13285

  • Hopital Saint Joseph /ID# 145560

    Marseille, Bouches-du-Rhone, 13285

  • Hopital Saint Joseph /ID# 145571

    Marseille, Bouches-du-Rhone, 13285

  • Hopital de la Timone /ID# 145558

    Marseille, Provence-Alpes-Côte d'Azur Region, 13385

  • Hopital de la Timone /ID# 145574

    Marseille, Provence-Alpes-Côte d'Azur Region, 13385

  • Hopital de la Timone /ID# 147237

    Marseille, 13385

  • Ctre Hosp de Montelimar /ID# 147239

    Montélimar, 26216

  • Hopital Saint Eloi /ID# 144919

    Montpellier, Herault, 34295

  • Cabinet Medical, Boyer Darrigr /ID# 145562

    Nanterre, 92000

  • CHU de Nice /ID# 144921

    Nice, 06202

  • Cabinet Medical, Dr. Verdier, /ID# 145575

    Nîmes, 30900

  • CHR Orleans - Hopital de la Source /ID# 147250

    Orléans, Centre-Val de Loire, 45067

  • Hopital Saint Antoine /ID# 145567

    Paris, 75012

  • Hopital Saint Antoine /ID# 148635

    Paris, 75012

  • Hopital Saint Antoine /ID# 148693

    Paris, 75012

  • Hopital Saint Antoine /ID# 152825

    Paris, 75012

  • Cabinet Medical, Giuily /ID# 145882

    Paris, 75016

  • Hopital Bichat-Claude Bernard /ID# 149246

    Paris, 75018

  • Cabinet Medical /ID# 145559

    Paris, 75020

  • Hopital Pitie Salpetriere /ID# 145556

    Paris, 75651

  • Hopital Pitie Salpetriere /ID# 145566

    Paris, 75651

  • Hopital Pitie Salpetriere /ID# 149337

    Paris, 75651

  • Hopital Bichat Claude Bernard /ID# 145886

    Paris, 75877

  • Hopital Tenon /ID# 145885

    Paris, 75970

  • CH Marechal Joffre /ID# 145875

    Perpignan, 66000

  • CHU Jean Bernard /ID# 147414

    Poitiers, 86021

  • CHU de Reims /ID# 148477

    Reims, 51092

  • Hospital Pontchaillou /ID# 145883

    Rennes, 35033

  • Charles Nicolle Hosp chu rouen /ID# 145557

    Rouen, 76031

  • Institut Arnault Tzanck /ID# 144925

    Saint-Laurent-du-Var, 06721

  • Hopital Begin /ID# 145872

    Saint-Mandé, 94160

  • CHU Strasbourg Hautepierre Hos /ID# 147246

    Strasbourg, 67200

  • Hopital Foch /ID# 147248

    Suresnes, 92151

  • Cabinet Medical, Dr. Constant, /ID# 145561

    Toulon, 83000

  • Hopital Universitaire Purpan /ID# 145869

    Toulouse, Haute-Garonne, 31059

  • Hopital Universitaire Purpan /ID# 150141

    Toulouse, Haute-Garonne, 31059

  • Clinique Amroise Pare /ID# 144924

    Toulouse, 31082

  • Hopital Joseph Ducuing /ID# 152832

    Toulouse, 81059

  • Ctre Hospitalier de Tourcoing /ID# 145568

    Tourcoing, 59208

  • Cabinet Medical, Barbereau /ID# 145874

    Tours, 37100

  • Hopital Paul Brousse /ID# 145879

    Villejuif, 94800

  • Hopital Paul Brousse /ID# 147244

    Villejuif, 94800

  • Hopital Paul Brousse /ID# 147417

    Villejuif, 94800

Other trials in France

About this study

Official title: Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patients With Chronic Hepatitis C - An Observational Study in France

This study seeks to determine the effectiveness of the interferon-free ABBVIE REGIMEN ± ribavirin (RBV) in participants with chronic hepatitis C (CHC) virus in clinical practices across France.

Keywords
HCV, Chronic Hepatitis C
Medical subject headings
Hepatitis C, Chronic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT02618928
Study groupRoleWhat they receive
Paritaprevir/Ritonavir + Ombitasvir ± Dasabuvir ± RibavirinParticipants in this observational study received treatment with paritaprevir/ritonavir (r) and ombitasvir with or without dasabuvir ± ribavirin (RBV) for 8, 12, or 24 weeks for the treatment of chronic hepatitis C (CHC), according to hepatitis C virus (HCV) genotype/subtype and stage of liver disease. The prescription of treatment regimen was at the discretion of the physician in accordance with local clinical practice and label, and was made independently from this observational study and preceded the decision to offer the patient the opportunity to participate in this study.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percentage of Participants Achieving Sustained Virological Response 12 Weeks Post-treatment (SVR12)

    Sustained virologic response was defined as hepatitis C virus ribonucleic acid (HCV RNA) levels less than 50 IU/mL 12 weeks after the last dose of study drug. Participants with missing HCV RNA were counted as virological failure.

    Measured: 12 weeks after the last dose of study drug (week 20, 24, or 36 depending on the treatment regimen)

Secondary outcomes (24)
  1. Percentage of Participants Achieving Virological Response at End of Treatment

    Virologic response was defined as hepatitis C virus ribonucleic acid (HCV RNA) levels less than 50 IU/mL.

    Measured: End of treatment (week 8, 12, or 24 depending on the treatment regimen)

  2. Percentage of Participants With Sufficient Follow-up Who Achieved Sustained Virological Response 12 Weeks Post-treatment

    Sustained virologic response was defined as hepatitis C virus ribonucleic acid (HCV RNA) levels less than 50 IU/mL 12 weeks after the last dose of study drug.

    The Core Population with sufficient follow-up data regarding SVR12 included all core population participants who

    • had evaluable HCV RNA data ≥ 70 days after the last actual dose of the ABBVIE REGIMEN
    • or a HCV RNA value ≥ 50 IU/mL at the last measurement post-baseline
    • or had HCV RNA < 50 IU/mL at the last measurement post-baseline, but no HCV RNA measurement ≥ 70 days after the last actual dose of the ABBVIE REGIMEN due to reasons related to safety (e.g. dropped out due to adverse event) or virologic failure.

    Measured: 12 weeks after the last dose of study drug (week 20, 24, or 36 depending on the treatment regimen)

  3. Percentage of Participants With Relapse

    Relapse was defined as participants with a virologic response (VR; HCV RNA < 50 IU/mL) at end of treatment (EOT) followed by HCV RNA ≥ 50 IU/mL at any time after the end of treatment.

    Measured: End of treatment (week 8, 12, or 24 depending on the treatment regimen) and up to 24 weeks after the end of treatment.

  4. Percentage of Participants With Breakthrough

    Breakthrough was defined as at least one documented HCV RNA < 50 IU/mL followed by HCV RNA ≥ 50 IU/mL during treatment.

    Measured: 8, 12, or 24 weeks (depending on the treatment regimen)

  5. Percentage of Participants With Rapid Virological Response at Week 4 (RVR4)

    RVR 4 was defined as participants with HCV RNA < 50 IU/mL at week 4.

    Measured: Week 4

  6. Percentage of Participants With Sufficient Follow-up Who Achieved Sustained Virological Response 24 Weeks Post-treatment (SVR24)

    Sustained virologic response was defined as hepatitis C virus ribonucleic acid (HCV RNA) levels less than 50 IU/mL 24 weeks after the last dose of study drug.

    The Core population with sufficient follow-up data regarding SVR24 included all core population participants who

    • had evaluable HCV RNA data ≥ 126 days after the last actual dose of the ABBVIE REGIMEN
    • or a HCV RNA value ≥ 50 IU/mL at the last measurement post-baseline
    • or had HCV RNA < 50 IU/mL at the last measurement post-baseline, but no HCV RNA measurement ≥ 126 days after the last actual dose of the ABBVIE REGIMEN due to reasons related to safety (e.g. dropped out due to adverse event) or virologic failure.

    Measured: 24 weeks after the last dose of study drug (week 32, 36, or 48 depending on the treatment regimen)

  7. Number of Participants in Each Non-response Category 12 Weeks Post-treatment

    SVR12 non-response was categorized according to the following:

    • On-treatment virologic failure (breakthrough [at least one documented HCV RNA < 50 IU/mL followed by HCV RNA ≥ 50 IU/mL during treatment] or failure to suppress [each measured on-treatment HCV RNA value ≥ 50 IU/mL]);
    • Relapse, defined as HCV RNA < 50 IU/mL at EOT followed by HCV RNA ≥ 50 IU/mL post-treatment in patients who completed treatment (not more than 7 days shortened);
    • Death
    • Premature treatment discontinuation with no on-treatment virologic failure;
    • Insufficient virological response reported or HCV RNA ≥ 50 IU/mL post-EOT and none of the above criteria
    • Missing SVR12 data and/or none of the above criteria.

    Measured: 12 weeks after the last dose of study drug (week 20, 24, or 36 depending on the treatment regimen)

  8. Percentage of Participants With Adherence to the ABBVIE Regimen, by Adherence Category

    Adherence to the ABBVIE treatment regimen is expressed as a percentage of the target dose and was calculated as:

    Cumulative dose taken / (initial prescribed dose * planned duration) * 100 The ABBVIE regimen consists of paritaprevir/r and ombitasvir with or without dasabuvir.

    Measured: From first dose of study drug to end of treatment, 8 to 24 weeks depending on the treatment regimen.

  9. Percentage of Participants With Adherence to Ribavirin by Adherence Category

    Adherence to ribavirin is expressed as a percentage of the target dose, and was calculated as:

    Cumulative dose taken / (initial prescribed dose * planned duration) * 100

    Measured: From first dose of study drug to end of treatment, 8 to 24 weeks depending on the treatment regimen.

  10. Percentage of Ribavirin Treatment Days in Relation to the Target Number of Ribavirin Treatment Days

    Measured: From first dose of study drug to end of treatment, 8 to 24 weeks depending on the treatment regimen.

  11. Number of Participants Who Received Concomitant Medications

    Concomitant medication other than for chronic hepatitis C used from the time when the decision was made to initiate treatment with paritaprevir/ritonavir and ombitasvir with or without dasabuvir until after the last dose.

    Measured: From first dose of study drug to end of treatment, 8 to 24 weeks depending on the treatment regimen

  12. Number of Participants With Adverse Events, Serious Adverse Events, or Pregnancies

    Measured: From first dose of study drug through 30 days after last dose (12 to 28 weeks depending on treatment regimen). The median (minimum, maximum) duration of treatment was 84 (4, 167) days.

  13. Change From Baseline in Fatigue Impact Scale Total Score

    The Fatigue Impact Scale (FIS) questionnaire was used to assess the impact of fatigue on the quality of life of patients.

    The FIS consists of 40 items, each of which is scored 0 (no problem) to 4 (extreme problem), providing a total score from of 0 to 160, where a lower score = less fatigue impact

    Measured: Baseline, end of treatment (week 8, 12, or 24 depending on the treatment regimen), and at 12 and 24 weeks after end of treatment

  14. Change From Baseline in EuroQol 5 Dimension 5 Level (EQ-5D-5L) Index Score

    The EQ-5D-5L is a health state utility instrument that evaluates preference for health status. The 5 items in the EQ-5D-5L comprise 5 dimensions (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) each of which are rated on 5 levels of severity (1: indicating no problem, 2: indicating slight problems, 3: indicating moderate problems, 4: indicating severe problems, 5: indicating extreme problems), and a separate visual analog scale (VAS).

    Responses to the 5 dimension scores were combined and converted into a single preference-weighted health utility index score by applying country-specific weights.The range for EQ-5D-5L index score is 0 to 1 where '0' is defined as a health state equivalent to being dead and '1' is full health.The higher the score the better the health status.

    Measured: Baseline, end of treatment (week 8, 12, or 24 depending on the treatment regimen), and at 12 and 24 weeks after end of treatment

  15. Change From Baseline in EuroQol 5 Dimension 5 Level (EQ-5D-5L) VAS Score

    The EQ-5D-5L is a health state utility instrument that evaluates preference for health status with a separate visual analog scale (VAS).

    The VAS assesses overall health on a scale from 0 (worst health imaginable) to 100 (best health imaginable).

    Measured: Baseline, end of treatment (week 8, 12, or 24 depending on the treatment regimen), and at 12 and 24 weeks after end of treatment

  16. Change From Baseline in Work Productivity and Activity Impairment (WPAI): Absenteeism

    The WPAI Hepatitis C V2.0 is an HCV specific questionnaire used to measure work absenteeism, work presenteeism, and daily activity impairment. Respondents were asked about time missed from work and time while at work during which productivity was impaired in the past seven days. Results of WPAI are expressed as a percentage of impairment from 0 to 100, with higher percentages indicating greater impairment and less productivity.

    Absenteeism indicates the percentage of work time missed due to health problems.

    Measured: Baseline, end of treatment (week 8, 12, or 24 depending on the treatment regimen), and at 12 and 24 weeks after end of treatment

  17. Change From Baseline in Work Productivity and Activity Impairment (WPAI): Presenteeism

    The WPAI Hepatitis C V2.0 is an HCV specific questionnaire used to measure work absenteeism, work presenteeism, and daily activity impairment. Respondents were asked about time missed from work and time while at work during which productivity was impaired in the past seven days. Results of WPAI are expressed as a percentage of impairment from 0 to 100, with higher percentages indicating greater impairment and less productivity.

    Presenteeism indicates the percentage of impairment while working due to health problems.

    Measured: Baseline, end of treatment (week 8, 12, or 24 depending on the treatment regimen), and at 12 and 24 weeks after end of treatment

  18. Change From Baseline in Work Productivity and Activity Impairment (WPAI): Total Work Productivity Impairment (TWP)

    The WPAI Hepatitis C V2.0 is an HCV specific questionnaire used to measure work absenteeism, work presenteeism, and daily activity impairment. Respondents were asked about time missed from work and time while at work during which productivity was impaired in the past seven days. Results of WPAI are expressed as a percentage of impairment from 0 to 100, with higher percentages indicating greater impairment and less productivity.

    Total work productivity impairment (TWP) indicates the percentage of overall work impairment due to health problems.

    Measured: Baseline, end of treatment (week 8, 12, or 24 depending on the treatment regimen), and at 12 and 24 weeks after end of treatment

  19. Change From Baseline in Work Productivity and Activity Impairment (WPAI): Total Activity Impairment

    The WPAI Hepatitis C V2.0 is an HCV specific questionnaire used to measure work absenteeism, work presenteeism, and daily activity impairment. Respondents were asked about time missed from work and time while at work during which productivity was impaired in the past seven days. Results of WPAI are expressed as a percentage of impairment from 0 to 100, with higher percentages indicating greater impairment and less productivity.

    Total activity impairment (TAI) indicates the percentage of general (non-work) activity impairment due to health problems.

    Measured: Baseline, end of treatment (week 8, 12, or 24 depending on the treatment regimen), and at 12 and 24 weeks after end of treatment

  20. Change From Baseline in Beliefs Medication Questionnaire - (18-item BMQ)

    The BMQ consists of 2 sections and 18 questions to screen for patients' beliefs, attitudes and concerns about their medication. The BMQ-Specific section comprises two 5-item subscales assessing the necessity of and concerns about the prescribed medication (Specific-Necessity and Specific-Concerns). The BMQ-General section comprises two 4-item subscales assessing beliefs that medicines are harmful and overused by doctors in general (General-Harm and General-Overuse). The 18 items are rated on a Likert scale from 1 (strongly disagree) to 5 (strongly agree). Each subscale score ranges from 1 to 5. High scores in the Specific-Concerns scale represent the notion that adverse reactions are potentially harmful when taking medication on a regular basis, and high scores in the Specific-Necessity scale indicate the patient's need to adhere to medication to maintain health. High scores in the General-Harm and General-Overuse scales represent an overall negative perception of medication.

    Measured: Baseline and end of treatment (week 8, 12, or 24 depending on the treatment regimen)

  21. Change From Baseline in Patient Activation Measure 13 (PAM-13)

    PAM 13 is a measure used to assess the patient knowledge, skill, and confidence for self-management, consisting of 13 questions. Each of the 13 items can be answered with one of four possible response options, which are "disagree strongly" (1), "disagree" (2), "agree" (3), "agree strongly" (4). Scores were summed to calculate the overall raw score, then transformed to a scale with a theoretical range 0 to 100, based on calibration tables, with higher PAM scores indicating higher patient activation.

    Measured: Baseline and end of treatment (week 8, 12, or 24 depending on the treatment regimen)

  22. Number of Participants With Outpatient Consultations Due to Liver Disease by Category

    Measured: From first dose of study drug through 30 days after last dose (12 to 28 weeks depending on treatment regimen). The median (minimum, maximum) duration of treatment was 84 (4, 167) days.

  23. Number of Participants With Hospitalizations Due to Liver Disease by Category

    Measured: From first dose of study drug through 30 days after last dose (12 to 28 weeks depending on treatment regimen). The median (minimum, maximum) duration of treatment was 84 (4, 167) days.

  24. Change From Baseline in Percent Glycosylated Hemoglobin (HbA1c)

    Measured: Baseline and end of treatment (week 8, 12, or 24 depending on the treatment regimen)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Dec 2015 (estimated)
  2. Study start15 Dec 2015
  3. Primary completion29 Mar 2018
  4. Study completion29 Mar 2018

Resources

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
Cohort
Time perspective
Prospective
Enrolment
735 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02618928
Sponsor's protocol ID
P15-405
Acronym
OPALE
Status last verified
Feb 2019
First submitted
24 Nov 2015
Last updated
17 Jun 2019
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Ferenci P, Bourgeois S, Buggisch P, Norris S, Curescu M, Larrey D, Marra F, Kleine H, Dorr P, Charafeddine M, Crown E, Bondin M, Back D, Flisiak R. Real-world safety and effectiveness of ombitasvir/paritaprevir/ritonavir +/- dasabuvir +/- ribavirin in hepatitis C virus genotype 1- and 4-infected patients with diverse comorbidities and comedications: A pooled analysis of post-marketing observational studies from 13 countries. J Viral Hepat. 2019 Jun;26(6):685-696. doi: 10.1111/jvh.13080. Epub 2019 Mar 5.

    PubMed 30739368

Questions about this trial

What is this clinical trial studying?

An observational study of Chronic Hepatitis C, run by AbbVie at 70 sites 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 3 inclusion and 1 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: finished, as of the sponsor's last update on 17 Jun 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 70 sites 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?

Yes. Results are posted in the registry (first posted 17 Jun 2019). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percentage of Participants Achieving Sustained Virological Response 12 Weeks Post-treatment (SVR12) (time frame: 12 weeks after the last dose of study drug (week 20, 24, or 36 depending on the treatment regimen)). 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 NCT02618928, which also lists 1 linked publication.

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 Jun 2019.

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