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NCT02782949Fut, nem toboroz2. fázis

Curcumin in Preventing Gastric Cancer in Patients With Chronic Atrophic Gastritis or Gastric Intestinal Metaplasia

Randomized, Double-Blind, Placebo-Controlled Trial of Meriva® (Curcuminoids) as a Candidate Chemoprevention Agent for Gastric Carcinogenesis

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. szept. 14.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

This randomized phase IIb trial studies how well curcumin works in preventing gastric cancer in patients with chronic atrophic gastritis and/or gastric intestinal metaplasia. Curcumin is an antioxidant compound found in plants that may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Állapot (regiszter)
Fut, nem toboroz
Fázis (regiszter)
2. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
50 (tényleges)
Első benyújtás
2016. máj. 25.
Kezdés
2017. ápr. 4.
Elsődleges befejezés
2022. okt. 6.
Fő szponzor
National Cancer Institute (NCI)
NCT-szám
NCT02782949

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó · 2. fázis
  • Bevont résztvevők: 50
  • 2017. ápr. 4. és az elsődleges befejezés (2022. okt. 6.) között
  • 2 helyszín, 2 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

Ki nem vehet részt

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Korábbi kezelés

  • History of colorectal cancer; exception: individuals with stage I or II colorectal cancer who have not received any chemotherapy
  • Receiving any other investigational agents
  • Use of any anticoagulation medications, such as warfarin or Coumadin
  • Pregnant or breast feeding; Note: Pregnant women are excluded from this study; because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with Meriva, breastfeeding should be discontinued if the mother is treated with Meriva
  • Receiving any other investigational, anticoagulation, and/or chemotherapy agents

Más betegség

  • Known diagnosis of human immunodeficiency virus (HIV); Note: An HIV screening test does not have to be performed to evaluate this criterion
  • History of gastric surgery
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to Meriva

Életkor

  • History of other malignancy =< 2 years prior to the registration/randomization evaluation, with the exception of basal cell or squamous cell skin cancer

Egyéb

  • PRE-REGISTRATION EXCLUSION CRITERIA
  • REGISTRATION/RANDOMIZATION EXCLUSION CRITERIA

Kiket keres a vizsgálat

  • PRE-REGISTRATION INCLUSION CRITERIA
  • Ability to understand and the willingness to sign a written informed consent document
  • Willingness to undergo screening tests and procedures
  • Willingness to provide blood and tissue samples for safety/toxicity monitoring and biomarker analyses
  • Willingness to avoid the use of curcumin or any over-the-counter or prescription medications containing curcumin or curcuminoids
  • REGISTRATION/RANDOMIZATION INCLUSION CRITERIA
  • Histologically-confirmed chronic multifocal atrophic gastritis (MAG) and/or gastric intestinal metaplasia (GIM)
  • Helicobacter pylori negative, defined as negative stool antigen testing and negative histological examination
  • Eastern Cooperative Oncology Group (ECOG) performance status =< 1
  • Aspartate transaminase (AST), alanine transferase (ALT) within institutional limits of normal or judged to be not clinically significant by the investigator
  • Alkaline phosphatase within institutional limits of normal or judged to be not clinically significant by the investigator
  • Platelets within institutional limits of normal or judged to be not clinically significant by the investigator
  • Hemoglobin within institutional limits of normal or judged to be not clinically significant by the investigator
  • White blood cells (WBC) within institutional limits of normal or judged to be not clinically significant by the investigator
  • Blood urea nitrogen (BUN) within institutional limits of normal or judged to be not clinically significant by the investigator
  • Total bilirubin within institutional limits of normal or judged to be not clinically significant by the investigator
  • Creatinine within institutional limits of normal or judged to be not clinically significant by the investigator
  • Not pregnant or breast feeding; Note: The effects of Meriva on the developing human fetus at the recommended therapeutic dose are unknown; for this reason, individuals of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her study physician immediately

Életkor a regiszterben: 21 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (2)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Hospital Regional de OccidenteSanta Rosa de CopánHondurasIsmeretlen állapot
University of Puerto RicoSan JuanPuerto RicoIsmeretlen állapot

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