このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Outpatient Pramlintide Study

2026年10月27日 更新者:Linda Lester、Oregon Health and Science University

An Outpatient Crossover Study to Evaluate Insulin and Pramlintide Versus Insulin Alone Delivery Strategy

The primary purpose of this study is to evaluate performance of a non-hybrid, fully automated closed loop system that does not require the person to announce meals to the system, and will utilize the hormone analog pramlintide in combination with insulin to potentially reduce the meal related hyperglycemia and increase the time spent in target range during the daytime.

調査の概要

研究の種類

介入

入学 (推定)

26

段階

  • 適用できない

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:Samrita Thapa, MPH
  • 電話番号:503-494-8421
  • メール:thapasa@ohsu.edu

研究連絡先のバックアップ

  • 名前:Peter Jacobs, PhD
  • 電話番号:503-418-9331
  • メール:jacobsp@ohsu.edu

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~70年 (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

説明

Inclusion Criteria:

  • Diagnosis of type 1 diabetes mellitus for at least 1 year.
  • Participants 18 to 70 years of age.
  • Current use of an insulin pump for at least 3 months with stable insulin pump settings for >2 weeks.
  • Uses a carbohydrate ratio, at least occasionally, to dose meal-time insulin
  • HbA1c ≤ 10.5% at screening.
  • Total daily insulin requirement is less than 139 units/day.
  • Lives with another person age 18 or older who will sleep in the house at night and that can attend the training on using the system.
  • Current use of a smartphone so can be contacted by study staff off-campus
  • Willingness to follow all study procedures, including attending all clinic visits.
  • Willingness to sign informed consent and HIPAA documents.

Exclusion Criteria:

  • Individual of childbearing potential who is pregnant or intending to become pregnant or breast-feeding, or is not using adequate contraceptive methods. Acceptable contraception includes birth control pill / patch / vaginal ring, Depo-Provera, Norplant, an IUD, the double barrier method (the woman uses a diaphragm and spermicide and the man uses a condom), or abstinence.
  • Any cardiovascular disease, defined as a clinically significant EKG abnormality at the time of screening or any history of: stroke, heart failure, myocardial infarction, angina pectoris, or coronary arterial bypass graft or angioplasty. Diagnosis of 2nd or 3rd degree heart block or any non-physiological arrhythmia judged by the investigator to be exclusionary.
  • Renal insufficiency (GFR < 60 ml/min, using the MDRD equation as reported by the site laboratory).
  • Liver failure, cirrhosis, or any other liver disease that compromises liver function as determined by the investigator.
  • History of severe hypoglycemia during the past 3 months prior to screening visit or hypoglycemia unawareness as judged by the investigator.
  • Participants will complete a hypoglycemia awareness questionnaire included in Appendix A. Participants will be excluded for four or more R responses.
  • History of diabetes ketoacidosis during the prior 3 months prior to screening visit, as diagnosed on hospital admission or as judged by the investigator.
  • Adrenal insufficiency.
  • Any active infection requiring treatment (example soft tissue infection requiring antibiotics).
  • Known or suspected abuse of alcohol, narcotics, or illicit drugs.
  • Seizure disorder.
  • Active foot ulceration.
  • Severe peripheral arterial disease characterized by ischemic rest pain or severe claudication.
  • Major surgical operation within 30 days prior to screening.
  • Use of an investigational drug within 30 days prior to screening.
  • Chronic usage of any immunosuppressive medication (such as cyclosporine, azathioprine, sirolimus, or tacrolimus).
  • Bleeding disorder, treatment with warfarin, or platelet count below 50,000.
  • Allergy to Aspart insulin.
  • Allergy or intolerance of pramlintide.
  • Current administration of oral or parenteral corticosteroids.
  • Any life-threatening disease, including malignant neoplasms and medical history of malignant neoplasms within the past 5 years prior to screening (except basal and squamous cell skin cancer).
  • Current use of beta blockers or non-dihydropyridine calcium channel blockers.
  • Current use of any medication that may lower glucose other than insulin or pramlintide (ex. use of liraglutide, metformin, empaglifozin etc) including the use of GLP1RA medications for weight loss (ex. Wegovy or Zepbound).
  • Gastroparesis or history of chronic nausea and/or frequent emesis.
  • Low carbohydrate diet at the time of screening defined as less than 50 grams of carbohydrate per day.
  • Any clinically significant disease or disorder which in the opinion of the Investigator may jeopardize the participant's safety or compliance with the protocol

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:ヘルスサービス研究
  • 割り当て:ランダム化
  • 介入モデル:クロスオーバー割り当て
  • 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
実験的:Insulin Only Arm

Participants will use the closed loop system with insulin only for managing blood sugar for 1 week. Insulin will be administered by an Omnipod. Sensor glucose will be measured by a Dexcom G6 CGM.

The Model Predictive Control (MPC) insulin infusion algorithm contains a model within the controller that takes as an input the aerobic metabolic expenditure in addition to the CGM and meal in puts. The algorithm uses heart rate and accelerometer data collected on the patient's body to calculate metabolic expenditure (METs). The METs then acts on the model for the insulin dynamics, whereby more energy expenditure and longer duration exercise can lead to a more substantial effect of insulin on the CGM. The MPC also has missed meal insulin bolus detection where the system will calculate the amount of insulin that was missed for a meal. The missed meal boluses can be delivered automatically without any input from the user. This feature can also be disabled. The device in this mode will administer insulin continuously for managing blood sugar.

実験的:Insulin and Pramlintide Arm

Participants will use the closed loop system with insulin and pramlintide for managing blood sugar for 1 week. Insulin and pramlintide will be administered by two Omnipods. Sensor glucose will be measured by a Dexcom G6 CGM.

The Model Predictive Control (MPC) insulin infusion algorithm contains a model within the controller that takes as an input the aerobic metabolic expenditure in addition to the CGM and meal in puts. The algorithm uses heart rate and accelerometer data collected on the patient's body to calculate metabolic expenditure (METs). The METs then acts on the model for the insulin dynamics, whereby more energy expenditure and longer duration exercise can lead to a more substantial effect of insulin on the CGM. The MPC also has missed meal insulin bolus detection where the system will calculate the amount of insulin that was missed for a meal. The missed meal boluses can be delivered automatically without any input from the user. This feature can also be disabled. The device in this mode will administer both insulin and pramlintide continuously for managing blood sugar. The system will deliver pramlintide in a fixed ratio to insulin at 6 mcg of pramlintide delivered for every 1 unit of insulin.

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
Percent of time with sensed glucose between 70-180 mg/dl
時間枠:12 hours following in-clinic visit

Blood glucose values are recorded every 5 minutes using the Dexcom G6 sensor. Percent of time in range can take values between 0 and 100 and uses the six hours following the meal as the denominator.

12 hours following in-clinic visit

二次結果の測定

結果測定
メジャーの説明
時間枠
Incremental area under the curve of postprandial glucose
時間枠:6 hours following the start of standarized in-clinic meal

Incremental area under the curve (iAUC) of postprandial glucose (mg/dL*min) calculated using a trapezoidal method, which sums all continuous glucose monitoring (CGM) values above the starting glucose for the observation period. Values shown are iAUC/1000.

6 hours following the start of standarized in-clinic meal
Percent of time with sensed glucose <70 mg/dl
時間枠:12 hours following in-clinic visits
12 hours following in-clinic visits
Percent of time with sensed glucose between 70 - 140 mg/dl
時間枠:12 hours following in-clinic visits

Blood glucose values are recorded every 5 minutes using the Dexcom G6 sensor. Percent of time in range can take values between 0 and 100 and uses the six hours following the meal as the denominator.

12 hours following in-clinic visits
Mean Sensed glucose
時間枠:12 hours following in-clinic visits
12 hours following in-clinic visits
Coefficient of variation of glucose
時間枠:12 hours following in-clinic visits
12 hours following in-clinic visits
Percent of time with sensed glucose <54 mg/dl
時間枠:12 hours following in-clinic visits
12 hours following in-clinic visits
Percent of time with sensed glucose >180 mg/dl
時間枠:12 hours following in-clinic visits
12 hours following in-clinic visits
Percent of time with sensed glucose >250 mg/dl
時間枠:12 hours following in-clinic visits
12 hours following in-clinic visits
Mean amount of insulin delivered (in units and units/kg)
時間枠:12 hours following in-clinic visits
12 hours following in-clinic visits
Mean amount of pramlintide delivered (in mcg and mcg/kg)
時間枠:12 hours following in-clinic visits
12 hours following in-clinic visits
Percent of time with sensed glucose between 70-180 mg/dl
時間枠:12 hours following first meal in-clinic
12 hours following first meal in-clinic
Number of adverse events probably or possibly associated with Pramlintide administration
時間枠:After the completion of study, an average of 2 weeks
After the completion of study, an average of 2 weeks
Baxter Retching Faces VAS scale for standardized in-clinic meal
時間枠:After the completion of study, an average of 2 weeks
After the completion of study, an average of 2 weeks
Mean duration of gastrointestinal issues after standardized in-clinic meal as reported by participant on BARF VAS scale
時間枠:After the completion of study, an average of 2 weeks
After the completion of study, an average of 2 weeks
Episodes of carbohydrate intake to treat hypoglycemia
時間枠:After the completion of study, an average of 2 weeks
After the completion of study, an average of 2 weeks
Mean number of low glucose events / day whereby a single low glucose event is defined to start when the CGM drops below 70 mg/dL for at least three measurements and ends when the CGM rises above 69 mg/dL for at least three measurements
時間枠:After the completion of study, an average of 2 weeks
After the completion of study, an average of 2 weeks
Mean amount of insulin delivered (in units and units/kg)
時間枠:12 hours following first meal in-clinic
12 hours following first meal in-clinic

その他の成果指標

結果測定
時間枠
Mean amount of pramlintide delivered (in mcg and mcg/kg)
時間枠:12 hours following first meal in-clinic
12 hours following first meal in-clinic

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。

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11月2日

一次修了 (推定)

2027年1月31日

研究の完了 (推定)

2027年1月31日

試験登録日

最初に提出

2026年10月15日

QC基準を満たした最初の提出物

2026年10月27日

最初の投稿 (実際)

2026年11月3日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月3日

QC基準を満たした最後の更新が送信されました

2026年10月27日

最終確認日

2026年10月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • STUDY00029226
  • 1R01DK129382-01 (米国 NIH グラント/契約)

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

いいえ

米国FDA規制機器製品の研究

はい

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。

購読する