SARS-CoV-2 and Herpesvirus Inhibition for Ending Long COVID Dysfunction (SHIELD)
2026年5月14日 更新者:David Putrino、Icahn School of Medicine at Mount Sinai
SARS-CoV-2 and Herpesvirus Inhibition for Ending Long COVID Dysfunction (SHIELD)
The purpose of this research study is to test if the combination of three drugs, valacyclovir, celecoxib, and Paxlovid will decrease the symptoms of Long COVID in adults compared to a placebo (this does not contain the medications).
調査の概要
詳細な説明
This is an off-label, randomized, double-blind, active placebo-controlled, two-arm clinical trial of a combination of celecoxib, valacyclovir, and Paxlovid in adults with Long COVID.
This study aims to evaluate the safety and efficacy of the combination of celecoxib, valacyclovir, and Paxlovid in adults with Long COVID (LC).
Safety will be primarily measured through blood and urine measures.
Efficacy will be evaluated by measuring patient-reported outcomes.
研究の種類
介入
入学 (推定)
150
段階
- フェーズ2
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。
研究連絡先
- 名前:David Putrino, PhD
- 電話番号:212-241-7658
- メール:CoreResearch@mountsinai.org
研究場所
-
-
New York
-
New York、New York、アメリカ、10029
- The Cohen Center for Recovery from Complex Chronic Illnesses (CoRE)
-
コンタクト:
-
主任研究者:
- David Putrino, PhD
-
-
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
- 大人
- 高齢者
健康ボランティアの受け入れ
いいえ
説明
Inclusion Criteria:
- 18-65 years of age at the time of study entry
- Diagnosed with Long COVID
- Individuals of child-bearing potential must have a negative serum pregnancy test at screening and agree to on-site urine pregnancy testing at all subsequent study visits
- A urine drug screen performed at the Screening Visit must be negative for drugs of abuse such as methamphetamine, cocaine, phencyclidine (PCP), and non-disclosed amphetamines and opioids/opiates.
- Those with mild to moderate depression should be clinically stable for three months, without risk of suicidal ideation or behavior.
Exclusion Criteria:
- Breastfeeding, pregnant, or planning to become pregnant during the next six months.
- In the opinion of the Investigator, any clinically significant, uncontrolled, or unstable medical or surgical condition that could affect the individual's ability to participate in the study or potentially compromise their well-being while enrolled in the study.
- In the opinion of the Investigator or based on results of the HADS, evidence of a clinically significant psychiatric disorder, e.g., severe, unstable or poorly controlled depression, anxiety or obsessive-compulsive disorder; moderate or severe alcohol use disorder; substance use disorder other than mild cannabis use disorder; or any history of bipolar disorder, schizophrenia, schizoaffective disorder or other psychotic disorder.
- Currently meeting criteria for ME/CFS at the pre-screening or screening visit, or a prior confirmed diagnosis of ME/CFS within the last 5 years. This may be determined as part of the initial screening call or visit.
- Any anticipated need for surgery that in the opinion of the Principal Investigator or Sub-I might confound results or interfere with the participant's ability to comply with the protocol.
- Symptomatic and/or otherwise clinically significant cardiac disease
- Acute non-COVID systemic infection (e.g., HIV, hepatitis) or other active viral or bacterial infection during the screening/washout period or at the Baseline visit.
- Currently receiving chronic systemic corticosteroids (>5 mg prednisone daily, or equivalent)
- Routine treatment with warfarin, heparin, lithium, digoxin, amiodarone, isoniazid, phenytoin, fluconazole, methotrexate, probenecid, or raloxifene. Participants on these medications should not be screened.
- Uncontrolled sleep apnea.
- Use of chronic nucleoside analog antiviral suppression therapy within one month of the Screening Visit or requiring on average more than one acute treatment course every two months.
- Current use of celecoxib either alone or in combination with valacyclovir or famciclovir
- In the opinion of the Investigator, evidence of current drug or alcohol abuse or dependency, or history of abuse or dependence during the preceding 12 months.
- The participant has undergone a malabsorptive weight loss procedure (e.g., Roux-en-Y or other bypass procedure).
- Severe IBS-C or colonic inertia as evidenced by seven or more days between bowel movements.
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
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:4倍
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Combination Drug Therapy
For 14 weeks, receives valacyclovir and celecoxib initially, then addition of Paxlovid for 15 days while decreasing valacyclovir dose, and then returns to valacyclovir at the original dose later.
|
one to two 750mg capsules taken orally in the morning and evening
200mg capsules taken orally in the morning and evening
one (100mg ritonavir tablet and two 150mg nirmatrelvir tablets) taken orally in the morning and evening
|
|
プラセボコンパレーター:Placebo
For 14 weeks, receives matched placebo capsules and tablets
|
matching placebo capsules and tablets taken orally in the morning and evening
|
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 |
|---|---|---|
|
EQ-5D-5L Visual Analogue Scale (VAS)
時間枠:Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
The EQ VAS records the patient's self-rated health on a visual analogue scale where the endpoints are labelled 'The best health you can imagine' (100) and 'The worst health you can imagine' (0), with higher scores indicating better health state.
The VAS can be used as a quantitative measure of health outcome that reflects the patient's own judgement.
|
Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
The EuroQol Five-Dimensional Health Questionnaire (EQ-5D-5L)
時間枠:Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
The EQ-5D-5L is a validated, standardized, generic instrument that is a preference-based health- related quality of life questionnaire.
The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems.
The patient is asked to indicate their health state by ticking the box next to the most appropriate statement in each of the five dimensions.
This decision results in a 1-digit number that expresses the level selected for that dimension.
The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.
Full scale from 5 to 25, with higher score indicating poorer health outcomes.
|
Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
|
Patient-Reported Outcomes Measurement Information System 29 (PROMIS-29)
時間枠:Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
The PROMIS-29 v2.0 profile assesses pain intensity using a single 0-10 numeric rating item and seven health domains (physical function, fatigue, pain interference, depressive symptoms, anxiety, ability to participate in social roles and activities, and sleep disturbance) using four items per domain.
The values of all item responses are averaged to generate subscores for each dimension.
From these subscores, a global physical health score and a global mental health score are generated.
The scores are translated into T-scores according to a reference population with a mean of 50 and a standard deviation of 10.
|
Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
|
General Symptom Questionnaire (GSQ-30)
時間枠:Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
The General Symptom Questionnaire-30 (GSQ-30) is a valid and reliable instrument to assess symptom burden among patients with acute and post-treatment.
The GSQ-30 total score ranges from 0 to 120, with higher scores indicating a greater symptom burden.
|
Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
|
Patient Health Questionnaire (PHQ-9)
時間枠:Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
The PHQ-9 is a series of questions assessing presence and severity of depression symptoms.
It evaluates each of the DSM-IV depression criteria and scores the responses from 0 ("Not at all") to 3 ("Nearly every day").
PHQ-9 scores of 5, 10, 15, and 20 represented mild, moderate, moderately severe, and severe depression, respectively.
Full scale from 0-27, with higher score indicating more severe symptoms.
|
Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
|
Generalized Anxiety Disorder (GAD-7)
時間枠:Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
The GAD-7 is a 7-item scale developed and validated to identify generalized anxiety disorder and its severity.
It assesses the frequency of 7 anxiety symptoms and scores the responses from 0 ("Not at all") to 3 ("Nearly every day").
Total scores of 5, 10, and 15 correspond to mild, moderate, and severe generalized anxiety disorder, respectively.
Full scale from 0-21, with higher score indicating more symptoms.
|
Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
|
COLUMBIA-SUICIDE SEVERITY RATING SCALE (C-SSRS)
時間枠:Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
A suicide risk assessment tool that supports suicide risk assessment through a series of simple, plain-language questions that anyone can ask. The answers help users identify whether someone is at risk for suicide, assess the severity and immediacy of that risk, and gauge the level of support that the person needs. Full range from 0 (low intensity suicidal ideation to 9 (high intensity suicidal ideation). Higher score represents poorer health outcomes. |
Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
|
Neuro-QoL™ v2.0 Cognitive Function-Short Form
時間枠:Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
The Neuro-QoL Cognitive Function v2.0 short form assesses perceived difficulties in cognitive abilities, including memory, attention, decision making, planning, organizing, calculating, remembering, and learning.
The short form consists of 8 questions assessed on a 5-point Likert scale, resulting in a raw score range of 8 to 40.
A raw score is then converted to a T-score using conversion tables.
Scores 0.5 - 1.0 SD worse than the mean (T-score 40-45) = mild symptoms/impairment.
Scores 1.0 - 2.0 SD worse than the mean (T-score 30-40) = moderate symptoms/impairment.
Scores 2.0 SD or more worse than the mean (T-score below 30) = severe symptoms/impairment.
|
Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
|
Single-item Sleep Quality Scale (SQS)
時間枠:Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
The SQS is a visual analog scale that instructs respondents to rate their overall quality of sleep over a 7-day recall period from 0 to 10. Scores of 0, 1, 4, 7, and 10 correspond to terrible, poor, fair, good, and excellent, respectively.
Higher scores indicate better sleep quality.
|
Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20
|
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
- 主任研究者:David Putrino, PhD、Icahn School of Medicine at Mount Sinai
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 (推定)
2026年6月1日
一次修了 (推定)
2028年6月30日
研究の完了 (推定)
2028年6月30日
試験登録日
最初に提出
2026年5月14日
QC基準を満たした最初の提出物
2026年5月14日
最初の投稿 (実際)
2026年5月19日
学習記録の更新
投稿された最後の更新 (実際)
2026年5月19日
QC基準を満たした最後の更新が送信されました
2026年5月14日
最終確認日
2026年2月1日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
- 感染症後障害
- COVID-19(新型コロナウイルス感染症)
- 病理学的プロセス
- 慢性疾患
- 疾患の属性
- 気道感染症
- 感染症
- RNAウイルス感染症
- ウイルス病
- 気道疾患
- 肺疾患
- 肺炎、ウイルス
- 肺炎
- コロナウイルス感染症
- コロナウイルス感染症
- ニドウイルス感染症
- 病理学的状態、徴候および症状
- ポスト急性COVID-19症候群
- 硫黄化合物
- 有機化学物質
- 複素環化化合物、1リング
- 複素環化化合物
- 複素環化化合物、2リング
- 複素環化化合物、融合リング
- アゾール
- 炭化水素
- 炭化水素、周期的
- 炭化水素、芳香
- アミド
- グアニン
- ヒポキサンチン
- ピリノン
- プリン
- ベンゼン誘導体
- ベンゼンスルホンアミド
- スルホンアミド
- スルホン
- ピラゾール
- アシクロビル
- セレコキシブ
- バラシクロビル
- NirmatrelvirとRitonavirの薬物の組み合わせ
その他の研究ID番号
- STUDY-25-00948
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
いいえ
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
はい
米国FDA規制機器製品の研究
いいえ
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。