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NCT05774704RecruitingPhase 1/2

Curcumin and Retinal Study

Curcumin and Retinal Amyloid-beta Pilot Study

Source: ClinicalTrials.gov · Last updated 13 Jan 2026

Brief summary (registry, in English)

To test how two weeks of curcumin supplementation would cross the blood brain barrier (BBB) and attach to amyloid beta proteins, to assess the feasibility (safety and bioavailability), and to explore the resulting abundance/composition of gut microbiota.

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
60 (estimated)
First submitted
23 Feb 2023
Start date
21 Aug 2023
Primary completion date
31 Dec 2026
Lead sponsor
Texas Tech University Health Sciences Center
NCT number
NCT05774704

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 60
  • From 21 Aug 2023 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • Inclusion:
  • Both male and female, age 40 - 89 years.
  • Diagnosed with Aβ deposits in retina (peripheral superior quadrants)--to be confirmed after consent obtained. If there is documentation the potential participant has been diagnosed with Aβ deposits in retina within 6 months before the consent session, we will use this diagnosis/documentation for eligibility criteria. Otherwise, the ophthalmic exam will be repeated after consent is obtained for the study.
  • No pre-existing liver or kidney diseases by self-report.
    • Exclusion:
  • Patients with ocular diseases (macular degeneration, severe diabetes retinopathy)
  • Had used systemic antibiotics within 1 month prior to the start of the study intervention
  • Had taken any turmeric or curcumin products within 2 weeks prior to the start of the study intervention
  • Had a known allergy to black pepper
  • Women that are pregnant or breastfeeding

Age in the registry: 40 years to 89 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Texas Tech University Health Sciences Center
Coordinator of this site? Confirm its status
LubbockUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.