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Monitoring Liver Disease Progression in Hepatitis C/HIV Co-infected Patients With No-to-moderate Fibrosis, in Phnom Penh, Cambodia (HCV-Monitoring)

2017年8月22日 更新者:Institute of Tropical Medicine, Belgium

Monitoring Liver Disease Progression in Hepatitis C/HIV Co-infected Patients With No-to-moderate Fibrosis, in Phnom Penh, Cambodia (HCV-Monitoring)

Data on the progression of liver fibrosis in patients co-infected with HIV taking effective suppressive antiretroviral therapy with no fibrosis or mild-to-moderate fibrosis at baseline are scarce. This uncertainty is reflected in lack of clear guidance on the need for earlier (than F3-F4) treatment in co-infected patients.

Within our hepatitis C/HIV co-infection project in Cambodia, the investigators have the opportunity to monitor for short-term fibrosis progression in a cohort of co-infected patients with initial no-to-moderate fibrosis being identified during another ongoing study (HCV-Epi) and contribute relevant data to aid the risk/benefit analysis of postponing HCV treatment in HIV/HCV co-infected patients with initial fibrosis stage F0-F2.

The HCV-Monitoring study is a mono-centric prospective cohort study proposing a standardized follow-up (clinical, biological and imaging) to monitor for progression of hepatitis C disease in all patients with HIV infection (on anti-retroviral treatment or not) of Sihanouk Hospital Center of Hope (Phnom Penh, Cambodia) who have chronic HCV infection with GT-1, -2, -3 or -6 but are not considered in immediate need of HCV treatment.

All adult HIV-infected patients of the cohort (on ART or not yet on ART) of Sihanouk hospital Center of Hope who are identified during the HCV-Epi study having chronic HCV infection (all genotypes) and considered not in immediate need of HCV treatment (= Fibrosis stages F0-F2 and no clinical signs of extra-hepatic disease) will be considered for inclusion and invited to participate.

Approximately 70 HCV/HIV co-infected patients with no-to-moderate hepatic fibrosis will be enrolled in this study.

Beyond the baseline visit (HCV-Epi), follow-up visits are planned at 6, 12, 18 and 24 months. These patient visits will comprise of a history taking and physical examination focused on hepatic disease and blood sampling for basic hematologic and hepatic function parameters. Additionally, patients will be referred every year for ultrasound and transient elastography measurements and sampling for some additional liver function tests and measurement of HCV-RNA viral load.

調査の概要

状態

終了しました

条件

詳細な説明

Data on the progression of liver fibrosis in patients co-infected with HIV taking effective suppressive antiretroviral therapy with no fibrosis or mild-to-moderate fibrosis at baseline are scarce. This uncertainty is reflected in lack of clear guidance on the need for earlier (than F3-F4) treatment in co-infected patients.

Within our hepatitis C/HIV co-infection project in Cambodia, the investigators have the opportunity to monitor for short-term fibrosis progression in a cohort of co-infected patients with initial no-to-moderate fibrosis being identified during another ongoing study (HCV-Epi) and contribute relevant data to aid the risk/benefit analysis of postponing HCV treatment in HIV/HCV co-infected patients with initial fibrosis stage F0-F2.

The HCV-Monitoring study is a mono-centric prospective cohort study proposing a standardized follow-up (clinical, biological and imaging) to monitor for progression of hepatitis C disease in all patients with HIV infection (on anti-retroviral treatment or not) of Sihanouk Hospital Center of Hope (Phnom Penh, Cambodia) who have chronic HCV infection with GT-1, -2, -3 or -6 but are not considered in immediate need of HCV treatment.

The study will be conducted in Sihanouk Hospital Center of Hope (SHCH) in Phnom Penh (Cambodia), more particularly within the ambulatory HIV clinic setting. SHCH is a non-governmental hospital providing comprehensive HIV care free of charge since March 2003, as part of the national antiretroviral (ARV) program. They dispose of an experienced HIV clinician, counselor and social worker team and several operational research studies were conducted within this setting.

All adult HIV-infected patients of the cohort (on ART or not yet on ART) of Sihanouk hospital Center of Hope who are identified during the HCV-Epi study having chronic HCV infection (all genotypes) and considered not in immediate need of HCV treatment (= Fibrosis stages F0-F2 and no clinical signs of extra-hepatic disease) will be considered for inclusion and invited to participate.

Approximately 70 HCV/HIV co-infected patients with no-to-moderate hepatic fibrosis will be enrolled in this study. No formal sample size is being calculated. The final sample will comprise all patients fulfilling the inclusion criteria.

The data collected from the HCV-Epi study will be considered as the baseline visit for the HCV-Monitoring study. Thereafter, visits are planned at 6, 12, 18 and 24 months follow-up. These patient visits will, beyond the habitual HIV follow-up, integrate a history taking and physical examination focused on hepatic disease and blood sampling for basic hematologic and hepatic function parameters. Additionally, patients will be referred every year for ultrasound and transient elastography measurements and sampling for some additional liver function tests and measurement of HCV-RNA viral load.

研究の種類

観察的

入学 (予想される)

70

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Phnom Penh、カンボジア
        • Sihanouk Hospital Center of HOPE (SHCH), Cambodia

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

サンプリング方法

非確率サンプル

調査対象母集団

Adult HIV-infected patients of the SHCH cohort who have chronic HCV infection (all genotypes) with no-to-moderate hepatic fibrosis and not considered in immediate need of HCV treatment.

説明

Inclusion Criteria:

  • Male and females
  • ≥18 years
  • Documented HIV infection
  • Evidence of infection with hepatitis C virus (all genotypes): Positive anti-HCV antibody and HCV RNA
  • Absence of advanced liver disease or clinical signs of extra-hepatic disease:

    • F0-F2 (< 9,5 kPa) established by transient elastography, and
    • No clinical signs of extra-hepatic disease
  • Not on HCV antiviral treatment

Exclusion Criteria:

  • Currently on/or history of hepatitis C treatment
  • Patients with initial fibrosis stage ≥ F3 (≥ 9,5 kPA on transient elastography)
  • Patients not able/willing to adhere to the consultation, laboratory and liver stiffness measurement testing schedule as proposed in this study

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 観測モデル:コホート
  • 時間の展望:見込みのある

コホートと介入

グループ/コホート
介入・治療
HCV coinfection with no-to-moderate fibrosis
A history taking and physical examination focused on hepatic disease and blood sampling for basic hematologic and hepatic function parameters will be performed. Patients will also be referred every year for ultrasound and transient elastography measurements and sampling for some additional liver function tests and measurement of HCV-RNA viral load.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Short-term progression to advanced liver fibrosis
時間枠:30 months
Proportion of patients who progress to advanced liver fibrosis (F≥3; LSM ≥9.5 kPa).
30 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Demographic characteristics
時間枠:Baseline
Demographic baseline characteristics of the study participants
Baseline
Clinical characteristics
時間枠:Baseline
Clinical baseline characteristics of the study participants
Baseline
Laboratory characteristics
時間枠:Baseline
Laboratory baseline characteristics of the study participants
Baseline
Progression to cirrhosis
時間枠:30 months
Proportion of patients who progress to cirrhosis ((F=4, > 14 kPa)
30 months
Liver stiffness measurement
時間枠:30 months
Median Liver stiffness measurement increase per year
30 months
Changes in fibrosis stage scores
時間枠:30 months
Change in Metavir score (regression/progression, number of stages difference)
30 months
Diagnostic accuracy of non-invasive serum bio-markers: APRI
時間枠:30 months
Predictive value of APRI to identify a shift from (≤F2) to advanced fibrosis (≥3)
30 months
Diagnostic accuracy of non-invasive serum bio-markers: FIB-4
時間枠:30 months
Predictive value of FIB-4 to identify a shift from (≤F2) to advanced fibrosis (≥3)
30 months
Predictive factors for liver fibrosis progression
時間枠:30 months
Factors associated with rapid fibrosis progression in HCV/HIV coinfected patients with initial mild to moderate fibrosis: age, gender, alcohol use, smoking, coffee consumption, comorbidities, liver enzymes, HCV viral load, HIV viral load, and ART exposure
30 months

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • スタディディレクター:Anja De Weggheleire, MD、Institute of Tropical Medicine, Antwerp, Belgium
  • 主任研究者:An Sokkab, MD、Sihanouk Hospital Center of HOPE (SHCH), Cambodia

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2015年12月17日

一次修了 (実際)

2017年7月12日

研究の完了 (実際)

2017年7月12日

試験登録日

最初に提出

2015年11月25日

QC基準を満たした最初の提出物

2015年12月9日

最初の投稿 (見積もり)

2015年12月11日

学習記録の更新

投稿された最後の更新 (実際)

2017年8月23日

QC基準を満たした最後の更新が送信されました

2017年8月22日

最終確認日

2017年8月1日

詳しくは

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医薬品およびデバイス情報、研究文書

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米国FDA規制機器製品の研究

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米国で製造され、米国から輸出された製品。

いいえ

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