A Gastrointestinal Quality of Life Study in Lung Transplant Recipients Converted From Mycophenolate Mofetil to Myfortic
Reduced Gastrointestinal Complaints and Improved Quality of Life in Lung Transplant Recipients Converted From Mycophenolate Mofetil (MMF) to Myfortic (Enteric-coated Mycophenolate Sodium, Ec-mps)
調査の概要
詳細な説明
Subjects administered MMF as part of their immunosuppression regimen after lung transplantation have a high incidence of GI symptoms related to the known side-effects of this drug. Previous studies have shown that GI symptoms are an important predictor of health related quality of life in other solid organ transplants (1). GI complications are common after lung transplant (2). We hypothesize that lung transplant patients converted from MMF to Myfortic will have significant reduction in severity of GI complaints. We also hypothesize that improvement in the severity of GI complaints will lead to an improved quality of life in these subjects. The study also includes data to evaluate the effect of GI complaints on health related quality of life.
Patients will complete questionnaires at each visit. Calls from the patients to the lung transplant center with GI complaints will be queried and documented on the case report form by the research nurse at each study visit. Similarly, hospital admissions for GI related complaints in the cohort will be documented. Symptom severity and health related quality of life will be assessed through the following questionnaires that have previously been validated in populations other than lung transplant (1). These questionnaires are selected specifically to capture the impact of GI complaints as related to the health related quality of life. The questionnaires that will be completed by the patient:
i.Gastrointestinal Quality of Life Index (GIQLI)
• The GIQLI is a 36-item questionnaire that assess the impact of GI distress on daily life
ii.SF-36 Health Survey • "The SF-36 Health Survey is a questionnaire that capture practical, reliable, and valid information about functional health and well-being from the patients' point of view" (4)
iii.EQ-5D Health Questionnaire
• "The EQ-5D is a standardized instrument for use as a measure of health outcome. The EQ-5D provides a simple descriptive profile and a single value for health status" (5)
Patients will complete the three questionnaires at 4 outpatient visits occurring:
- when the patient comes in to an outpatient clinic visit after initial hospital discharge after lung transplantation with complaints of GI distress (Day 1-Convert to Myfortic);
- 60 Days;
- 90 days;
- 180 days
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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Tennessee
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Nashville、Tennessee、アメリカ、37232-4753
- Vanderbilt University Medical Center
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Ability and willingness to provide written informed consent and adhere to study regimen
- Recipients who are 18-70 years of age
- Patients who have undergone either single or double lung transplant are discharged on the standard MMF (no generic MMF will be used) therapy and complain of GI symptoms, thought to be related to their immunosuppressive regimen
Exclusion Criteria:
- Patients who have GI complaints thought to be due to factors other than immunosuppressive regimen
- Patients receiving steroid treatment for acute rejection
- Women of childbearing potential who do not agree to use at least two acceptable forms of contraception prior to starting study drug, while taking study drug, and for 6 weeks after stopping study drug
- Women who have a positive serum or urine pregnancy test at visit 1 and/or continuing through the study
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:他の
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
他の:Patients taking Myfortic
Lung transplant patients converted from MMF to Myfortic as part of standard of care treatment will have GI and Quality of Life assessments done at the time of conversion to Myfortic and at 60 days, 90 days and 180 days.
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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 |
|---|---|---|
|
Change in Gastrointestinal Quality of Life Index (GIQLI), Baseline to 60 days:
時間枠:Change from Baseline to 60 days
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Change in GIQLI after conversion from MMF to Myfortic
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Change from Baseline to 60 days
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Change in SF-36 Health Survey, Baseline to 60 days
時間枠:Change from Baseline to 60 days
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Change in SF-36 Health Survey after conversion from MMF to Myfortic
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Change from Baseline to 60 days
|
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Change in EQ-5D Health Questionnaire, Baseline to 90 days
時間枠:Change from Baseline to 60 days
|
Change in EQ-5D Health Questionnaire after conversion from MMF to Myfortic
|
Change from Baseline to 60 days
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Gastrointestinal Quality of Life Index (GIQLI)
時間枠:Day 90 and Day 180
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Change in GIQLI after conversion from MMF to Myfortic
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Day 90 and Day 180
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SF-36 Health Survey
時間枠:Day 90 and Day 180
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Change in SF-36 Health Survey after conversion from MMF to Myfortic
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Day 90 and Day 180
|
|
EQ-5D Health Questionnaire
時間枠:Day 90 and Day 180
|
Change in EQ-5D Health Questionnaire after conversion from MMF to Myfortic
|
Day 90 and Day 180
|
協力者と研究者
スポンサー
捜査官
- 主任研究者:Eric Lambright, MD、Vanderbilt University Medcial Center
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- Myfortic 091423
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
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