THC Versus THC/CBD Versus Placebo to Improve Sleep Quality for Patients With Solid Organ Cancer and Insomnia
2026年8月31日 更新者:Mayo Clinic
MC251001 - Phase II Randomized Double-Blinded Pilot Study of THC vs. THC/CBD (1:1) vs. Placebo for Insomnia in Patients With Cancer
This phase II trial compares THC versus (vs.)
THC with CBD vs. placebo to improve sleep quality for patients with solid organ cancer and insomnia.
Many patients who are diagnosed with cancer struggle with sleep disorders after receiving a diagnosis.
Insomnia is the most reported sleep disturbance amongst cancer patients, often stemming from physical changes from tumor growth and surgery, side effects from supportive care and chemotherapy, and stress associated with the diagnosis.
THC with or without CBD may improve insomnia symptoms and sleep quality.
調査の概要
状態
まだ募集していません
研究の種類
介入
入学 (推定)
69
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:Clinical Trials Referral Office
- 電話番号:855-776-0015
- メール:mayocliniccancerstudies@mayo.edu
研究連絡先のバックアップ
- 名前:Susie Lewis-Peters, RN
- 電話番号:507-266-1909
研究場所
-
-
Minnesota
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Rochester、Minnesota、アメリカ、55905
- Mayo Clinic in Rochester
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コンタクト:
- Clinical Trials Referral Office
- 電話番号:855-776-0015
- メール:mayocliniccancerstudies@mayo.edu
-
主任研究者:
- Stacy D. D'Andre, MD
-
コンタクト:
- Ali Meyer, RN
- 電話番号:507-266-1160
-
-
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:
- Age ≥ 25 years
- History of solid organ (not hematologic) cancer diagnosis (except patients with central nervous system [CNS] cancer who have history of seizures or untreated brain metastasis). Patients may be either in remission or have active disease. Patients must be considered medically fit by their treating physician to participate in the study
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2
- History of insomnia for which the patient would like an intervention
- Insomnia Severity Index Score ≥ 15. Patients can answer questions orally rather than completing worksheet, for screening only
- Willing to abstain from alcohol, anticholinergics, and benzodiazepines while on study
- If on opioids, must be a stable dose ≥ 30 days prior to randomization (no changes to prescriptions, this can include as needed [PRN] dosing) with no plans to increase during the study period
- White blood cell count (WBC) ≥ 3,000/mm^3 (obtained ≤ 30 days prior to randomization)
- Hemoglobin ≥ 8 g/dL (obtained ≤ 30 days prior to randomization)
- Platelet count ≥ 50,000/mm^3 (obtained ≤ 30 days prior to randomization)
- Alanine aminotransferase (ALT) or aspartate transaminase (AST) ≤ 3 x upper limit of normal (ULN) (obtained ≤ 30 days prior to randomization)
- Glomerular filtration rate (GFR) > 20 (obtained ≤ 30 days prior to randomization)
- Total bilirubin ≤ 1.5 x ULN (obtained ≤ 30 days prior to randomization)
- Negative pregnancy test done ≤ 7 days prior to registration, for persons of childbearing potential only
- Provide informed consent
- Ability to complete questionnaires and diary by themselves or with assistance
- Willingness to wear a home EEG monitor and have a blue-tooth device for recording (Smart phone, iPad)
- Normal urine toxicology screen ≤ 7 days prior to randomization (abstinence from cannabinoids and other common drugs of abuse: cocaine, benzodiazepines, and methamphetamines)
Exclusion Criteria:
Any of the following because this study involves an investigational agent whose genotoxic, mutagenic, and teratogenic effects on the developing fetus and newborn are unknown:
- Pregnant persons
- Nursing persons
- Persons of childbearing potential or are able to father a child who are unwilling to employ adequate contraception (e.g., hormonal methods, barrier methods, intrauterine device, abstinence) during the study and for 14 days after their last dose
- Currently using any other pharmacologic agents, over the counter medications or supplements to specifically treat insomnia for ≤ 7 days prior to randomization
- Known primary sleep disorder (restless leg syndrome [RLS], uncontrolled apnea, narcolepsy)
- Cannabis use ≤ 30 days prior to randomization
- Active cardiac disease (symptomatic congestive heart failure [CHF], arrhythmias, untreated coronary artery disease [CAD])
- On warfarin, topiramate, clobazam, or other high-risk CYP3A4 substrates (amiodarone, macrolides, verapamil, fluoxetine, clotrimazole, ketoconazole) per pharmacy review
- History of Human Papilloma Virus positive (HPV+) head and neck cancer
- Any concomitant medications that, in the judgment of the treating physician or pharmacist, could result in an adverse drug effect (increase in substrate level); pharmacy e-consult will be conducted for each patient to determine CYP interactions
- Patients with a history of psychotic disorders (including but not limited to schizophrenia, major depression with psychotic features, brief psychotic disorder). Patients with depression, manic/depression, or obsessive compulsive disorder (OCD) will need clearance from their mental health provider that these medical conditions are controlled and that the patient is appropriate for the study
- Any known hypersensitivity to cannabis
- Patients with CNS cancer or brain metastasis who have had or have seizures
- History of, or current substance use disorder
- Patients with electrocardiography (ECG) test with corrected QT interval (QTc) ≥ 450 msec for men and ≥ 470 msec for women
- Current or past suicidal ideation or suicidal behavior within the last year, as assessed with the Columbia-Suicide Severity Rating Scale (C-SSRS)
- Patients with history off falls in the past 6 months, or considered at risk for falling
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:支持療法
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Arm I (THC tincture)
Patients receive THC tincture sublingually 60 minutes prior to bedtime QD on days 1-28.
Patients start on day 1 at the lowest dose, for a minimum of 2 nights, and may increase the dose every 2 nights until they reach the maximum dose or they have acceptable sleep and remain at that dose.
On days 29-34, patients continue to receive THC tincture sublingually 60 minutes prior to bedtime QD but titrate down to the lowest dose by day 34.
Treatment is given in the absence of disease progression or unacceptable toxicity.
Patients undergo blood and urine sample collection throughout the study.
|
採血を受ける
他の名前:
Given THC tincture sublingually
他の名前:
Given THC/CBD tincture sublingually
他の名前:
|
|
実験的:Arm II (THC/CBD tincture)
Patients receive THC/CBD tincture sublingually 60 minutes prior to bedtime QD on days 1-28.
Patients start on day 1 at the lowest dose, for a minimum of 2 nights, and may increase the dose every 2 nights until they reach the maximum dose or they have acceptable sleep and remain at that dose.
On days 29-34, patients continue to receive THC/CBD tincture sublingually 60 minutes prior to bedtime QD but titrate down to the lowest dose by day 34.
Treatment is given in the absence of disease progression or unacceptable toxicity.
Patients undergo blood and urine sample collection throughout the study.
|
採血を受ける
他の名前:
Given THC tincture sublingually
他の名前:
Given THC/CBD tincture sublingually
他の名前:
|
|
プラセボコンパレーター:Arm III (placebo tincture)
Patients receive placebo tincture sublingually 60 minutes prior to bedtime QD on days 1-28.
Patients start on day 1 at the lowest dose, for a minimum of 2 nights, and may increase the dose every 2 nights until they reach the maximum dose or they have acceptable sleep and remain at that dose.
On days 29-34, patients continue to receive placebo tincture sublingually 60 minutes prior to bedtime QD but titrate down to the lowest dose by day 34.
Treatment is given in the absence of disease progression or unacceptable toxicity.
Patients undergo blood and urine sample collection throughout the study.
|
採血を受ける
他の名前:
Given placebo tincture sublingually
|
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 Insomnia Sleep Index score
時間枠:From baseline to week 4
|
The Insomnia Sleep Index (ISI) is a brief screening tool used to assess insomnia symptoms and sleep patterns over the past week.
It consists of 7 questions answered on a scale of 0 (not al all) to 4 (not very much).
Total scores range from 0-28 with higher scores indicating greater severity of clinical insomnia.
|
From baseline to week 4
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change in Quality of Life Score
時間枠:From baseline to 4 weeks
|
Assessed using the Linear Analog Scale Assessment (LASA) of Quality of Life (QOL) scale, which consists of a single question related to quality of life over the past week.
The scale is answered on a scale of 0 (worst it can be) to 10 (best it can be).
Total scores range from 0-10 with higher scores indicating greater quality of life.
|
From baseline to 4 weeks
|
|
Change in Daytime Sleepiness
時間枠:From baseline to end of treatment (day 35)
|
As measured by the Patient-Reported Outcomes Measurement Information System Fatigue (PROMIS-Fatigue) Item Bank instrument.
The PROMIS-Fatigue questionnaire, a subscale of the PROMIS-29, measures fatigue and related symptoms over the past seven days.
It consists of four items rated on a scale of 1(not at all) to 5 (very much).
Total scores range from 4-20 with higher scores indicating greater experience of fatigue.
|
From baseline to end of treatment (day 35)
|
|
Average amount of deep sleep
時間枠:From baseline to week 4
|
As measured by home electroencephalography (EEG).
Will compare pair-wise between the three treatment arms.
Will be compared using the same methodology as used for the primary endpoint.
|
From baseline to week 4
|
|
Average amount of light REM sleep
時間枠:From baseline to week 4
|
As measured by home EEG.
Will compare pair-wise between the three treatment arms.
Will be compared using the same methodology as used for the primary endpoint.
|
From baseline to week 4
|
|
Average time awake
時間枠:From baseline to week 4
|
As measured by home EEG.
Will compare pair-wise between the three treatment arms.
Will be compared using the same methodology as used for the primary endpoint.
|
From baseline to week 4
|
|
Amount of sleep per day
時間枠:From baseline to week 4
|
As measured by home EEG.
Will compare pair-wise between the three treatment arms.
Will be compared using the same methodology as used for the primary endpoint.
|
From baseline to week 4
|
|
Change in mood - PHQ-9
時間枠:From baseline to end of treatment (day 35)
|
The Patient Health Questionnaire 9-item (PHQ-9) scale is a self-report questionnaire used to assess severity of depression over the last 2 weeks.
The PHQ-9 consists of nine items rated on a scale of 0 (not at all) to 3 (nearly every day).
Total scores range from 0-27 with higher scores indicating greater severity of depression symptoms.
|
From baseline to end of treatment (day 35)
|
|
Change in mood - GAD-7
時間枠:From baseline to end of treatment (day 35)
|
The General Anxiety Disorder 7-item (GAD 7) scale is used to assess symptoms and feelings of anxiety over the past two weeks.
The GAD-7 consists of 7 questions answered on a scale of 0 (not at all) to 3 (nearly every day).
The total score ranges from 0 to 21 with higher scores indicating more severe anxiety symptoms.
|
From baseline to end of treatment (day 35)
|
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。
スポンサー
捜査官
- 主任研究者:Stacy D. D'Andre, MD、Mayo Clinic in Rochester
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
便利なリンク
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10月1日
一次修了 (推定)
2027年9月1日
研究の完了 (推定)
2027年9月1日
試験登録日
最初に提出
2026年4月24日
QC基準を満たした最初の提出物
2026年4月24日
最初の投稿 (実際)
2026年5月4日
学習記録の更新
投稿された最後の更新 (実際)
2026年9月2日
QC基準を満たした最後の更新が送信されました
2026年8月31日
最終確認日
2026年8月1日
詳しくは
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。