- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07566325
Assess the Effects of Replacing Foods High in Refined Carbohydrates With Avocado on Biomarkers of Inflammation.
24 sierpnia 2026 zaktualizowane przez: Midwest Center for Metabolic and Cardiovascular Research
Effects of Avocado Consumption on Inflammation and Insulin Sensitivity in Adults With Elevated High Sensitivity-C-reactive Protein (Hs-CRP): A Randomized, Controlled Crossover Trial
The objective of this trial is to assess the effects of replacing foods high in refined carbohydrates, particularly added sugars, with avocado (isocaloric substitution) on biomarkers of inflammation and insulin sensitivity in adults with elevated hs-CRP and central adiposity.
Eligible participants will complete two 4-week interventions (1 avocado/d and control) separated by a 2-week washout phase.
Participants will complete a total of 7 clinic visits including one screening visit (visit 1, -7 days), one baseline visit (visit 2, day 0), two visits during each 4-week diet condition (visit 3 & 6 on day 21 and visits 4 & 7 on day 28), and one visit at the conclusion of the washout phase/start of the second condition (visit 5, day 0).
Przegląd badań
Status
Rekrutacyjny
Warunki
Interwencja / Leczenie
Typ studiów
Interwencyjne
Zapisy (Szacowany)
38
Faza
- Nie dotyczy
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Kontakt w sprawie studiów
- Nazwa: Sara Campbell
- Numer telefonu: 630-469-6600
- E-mail: scampbell@mbclinicalresearch.com
Kopia zapasowa kontaktu do badania
- Nazwa: Caryn Adams
- E-mail: cwolfe@mbclinicalresearch.com
Lokalizacje studiów
-
-
Illinois
-
Chicago, Illinois, Stany Zjednoczone, 60616
- Rekrutacyjny
- Illinois Institute of Technology
-
Kontakt:
- Chelsea Preiss
- Numer telefonu: 312-567-5300
- E-mail: cpreiss@illinoistech.edu
-
-
Nevada
-
Las Vegas, Nevada, Stany Zjednoczone, 89154
- Jeszcze nie rekrutacja
- University of Nevada, Las Vegas
-
Kontakt:
- Neda Akhavan
- Numer telefonu: 702-895-3011
- E-mail: neda.akhavan@unlv.edu
-
-
Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Tak
Opis
Inclusion Criteria:
- Male or female 21 - 74 years of age, inclusive;
- Baseline hs-CRP ≥2 to <10 mg/L;
- Central adiposity (waist circumference ≥35 inches in women and ≥40 inches in men);
- Body mass index 25.0 to 39.9 kg/m2;
- Normally active and judged by the Investigator to be in generally good health, based on medical history and screening measurements;
- Willing to consume daily study foods during each diet condition;
- Willing to maintain his/her regular physical activity pattern throughout the study period;
- Willing to follow test day instructions (refrain from consumption of alcoholic beverages and participation in vigorous physical activity for 24 hours and tobacco and caffeine for 1 hour prior to each test visit);
- No plans to change smoking, vaping, or other nicotine use habits during the study period; and
- Premenopausal women that are not using hormonal contraceptives must have a history of regular menstrual cycles (21-35 days per cycle) for at least 3 months prior to visit 1;
- Understands the study procedures and signs forms documenting informed consent to participate in the study and authorization for release of relevant protected health information to the study Investigator and is willing to complete study procedures.
Exclusion Criteria:
- Calculated energy needs of <1800 kcal/d per the Mifflin-St. Jeor Equation, with an adjustment for energy expended in physical activity;
- Known metabolic disease (e.g., type 1 or type 2 diabetes, metabolic dysfunction-associated steatohepatitis, etc.);
- Laboratory test result(s) of clinical significance based on the judgment of the Principal Investigator or qualified designee, including fasting glucose ≥126 mg/dL;
- Positive urine test for illicit drugs at visit 1;
- Clinical atherosclerotic disease;
- History or presence of clinically significant gastrointestinal, endocrine, renal, hepatic, hematologic, immunologic, dermatologic, pulmonary, pancreatic, neurologic, psychiatric, inflammatory or biliary disorder that, in the opinion of the Investigator, could interfere with the interpretation of the study results;
- History of cancer in the prior 2 years, except for non- melanoma skin cancer or carcinoma in situ of the cervix;
- Uncontrolled hypertension (systolic blood pressure ≥160 mm Hg and/or diastolic blood pressure ≥100 mm Hg) at screening;
- Unstable use (defined as initiation or change in dose) of anti-hypertensive medication within 4 weeks of visit 1;
- Unstable use (defined as initiation or change in dose) of thyroid hormone replacement medication within 12 weeks of visit 1;
- Use of beta-adrenergic blockers and/or high-dose (>25 mg/d) thiazide diuretics within 4 weeks of visit 1;
- Use of diabetes medications including glucagon-like peptide-1 (GLP-1) receptor agonists, GLP-1/glucose-dependent insulinotropic polypeptide (GIP) receptor agonists, alpha-glucosidase inhibitors, biguanides and biguanide combinations, thiazolidinediones, dipeptidyl peptidase-4 (DPP-4) inhibitors, meglitinides and sulfonylureas and combination sulfonylureas within 4 weeks of visit 1;
- Unstable use (defined as initiation or change in dose, agent, or regimen) of statins within 4 weeks of visit 1;
- Use of lipid-altering drugs other than statins including, but not limited to bile acid sequestrants, cholesterol absorption inhibitors, or fibrates within 4 weeks of visit 1;
- Use of any prescription medication with known effects on inflammation (e.g., colchicine, systemic corticosteroids) within 4 weeks of visit 1;
- Frequent use (≥4 doses/week) of non-steroidal anti-inflammatory drugs (NSAID) within 2 weeks of visit 2;
- Use of weight-loss drugs (including over-the-counter medications and/or supplements) or participation in a structured weight loss program within 4 weeks prior to visit 1;
- Unstable use (initiation or change in dose) within 4 weeks of visit 1 of sex hormones. Multiphasic hormonal contraceptives in which the amount of sex hormone in the active pill varies by week (i.e., biphasic, triphasic, quadriphasic) are considered unstable doses of sex hormones and are exclusionary;
- History of bariatric surgery or plans to have any surgery during the study;
- History of any major trauma or major surgical event within 2 months of visit 1;
- Use of herbs or dietary supplements that may affect lipid metabolism, including but not limited to omega-3 fatty acid supplements with >500 mg of eicosapentaenoic acid (EPA) and/or docosahexaenoic acid (DHA), niacin (or its analogs) at doses >200 mg/d, sterol/stanol products, dietary fiber supplements, red rice yeast supplements, garlic supplements, and soy isoflavone supplements within 2 weeks of visit 2;
- Use of herbs and dietary supplements that may affect carbohydrate metabolism, including chromium picolinate, ginseng, cinnamon (as a supplement) and starch blockers within 2 weeks of visit 2;
- Recent weight change of ±4.5 kg (~10 lbs.) within 3 months prior to visit 1;
- Has signs and symptoms of an active infection of clinical significance or has taken antibiotics within 5 days prior to any visit (washout is permitted by re-scheduling of the clinic visit);
- Extreme dietary habits (e.g., vegan, very low carbohydrate);
- History of an eating disorder (e.g., anorexia, bulimia nervosa, or binge eating) either diagnosed by a health professional or self-reported;
- Female who is pregnant, planning to be pregnant during the study period, lactating, or is of childbearing potential and is unwilling to commit to the use of a medically approved form of contraception throughout the study period;
- Known allergy, sensitivity, or intolerance to any components of the study foods;
- Exposed to any non-registered drug product within 4 weeks of visit 1;
- Currently participating in another research study;
- Use of hemp/marijuana products within 12 months of visit 1. Occasional use (e.g., once or twice a month) within 12 months of visit 1 is allowed but requires at least a 14-day washout prior to visit 2 and the participant must be willing to refrain from use during the study;
- Current or recent history (past 12 months of screening) or strong potential for illicit drug or alcohol abuse. Alcohol abuse will be defined as >14 drinks per week (1 drink = 12 oz beer, 5 oz wine, or 1.5 oz hard liquor); and
- Condition the Investigator believes would interfere with his or her ability to provide informed consent or comply with the study protocol, or which might confound the interpretation of the study results or put the person at undue risk.
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Inny
- Przydział: Randomizowane
- Model interwencyjny: Zadanie krzyżowe
- Maskowanie: Poczwórny
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: Avocado Group
1 avocado/day provided by 3 servings study products per day (muffins and pudding)
|
Active foods will provide the equivalent of one medium to large avocado/day in foods such as muffins and pudding, where avocado replaces refined carbohydrate, especially added sugars
|
|
Inny: Control Group
3 study products per day will be provided with energy from avocado will be replaced with refined carbohydrate, especially added sugars
|
Control foods will have similar energy contents to active foods, but energy from avocado will be replaced with refined carbohydrate, especially added sugars.
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Composite measure of inflammatory biomarkers
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change from baseline for a composite measure of inflammatory biomarkers including high-sensitivity C-reactive protein (hs-CRP), interleukin-6 (IL-6), interleukin-1 beta (IL-1β), interleukin-10 (IL-10), and tumor Necrosis Factor-alpha (TNF-α).
|
Change from baseline (day 0) to end of each condition (day 28)
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Homeostasis model assessments of insulin resistance (HOMA-IR)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Changes in (HOMA-IR)
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Homeostasis model assessments of β-cell function (HOMA-B)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Changes in HOMA-B
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Matsuda index of insulin sensitivity
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in Matsuda index of insulin sensitivity
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Disposition index
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in disposition index
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
high sensitivity C-reactive protein (hs-CRP)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in hs-CRP
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Interleukin-6 (IL-6)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in IL-6
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Interleukin-1 beta (IL-1β)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in IL-1β
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Interleukin-10 (IL-10)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in IL-10
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Tumor Necrosis Factor-alpha (TNF-α)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in TNF-α
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Fibrinogen
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in fibrinogen
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Soluble Intercellular Adhesion Molecule-1 (sICAM-1)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in sICAM-1
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Soluble Vascular Cell Adhesion Molecule-1 (sVCAM-1)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in sVCAM-1
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Total Cholesterol
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in total cholesterol
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Low-density lipoprotein cholesterol (LDL-C)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in LDL-C
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
High-density lipoprotein cholesterol (HDL-C)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in HDL-C
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Non-high-density lipoprotein cholesterol (non-HDL-C)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in non-HDL-C
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Triglycerides
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in triglycerides
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Apolipoprotein B (ApoB)
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in ApoB
|
Change from baseline (day 0) to end of each condition (day 28)
|
|
Systolic and diastolic blood pressures.
Ramy czasowe: Change from baseline (day 0) to end of each condition (day 28)
|
Change in resting, seated systolic and diastolic blood pressures.
|
Change from baseline (day 0) to end of each condition (day 28)
|
Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Współpracownicy
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
2 lipca 2026
Zakończenie podstawowe (Szacowany)
1 lutego 2027
Ukończenie studiów (Szacowany)
1 lutego 2027
Daty rejestracji na studia
Pierwszy przesłany
29 kwietnia 2026
Pierwszy przesłany, który spełnia kryteria kontroli jakości
29 kwietnia 2026
Pierwszy wysłany (Rzeczywisty)
5 maja 2026
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
27 sierpnia 2026
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
24 sierpnia 2026
Ostatnia weryfikacja
1 sierpnia 2026
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- MB-2544
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Nie
Bada produkt urządzenia regulowany przez amerykańską FDA
Nie
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .