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Colonic curcumin tissue levels in patients awaiting colorectal endoscopy or patients with colorectal cancer awaiting resection

A pilot study of the administration of curcumin to determine colonic curcumin tissue levels in patients awaiting colorectal endoscopy or patients with colorectal cancer awaiting resection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN93128659
Enrollment
30
Registered
2009-08-19
Start date
2009-07-01
Completion date
Unknown
Last updated
2018-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal cancer Cancer Malignant neoplasm of rectosigmoid junction

Interventions

1. Endoscopy but only as part of routine screening under the National Colorectal Cancer Screening Programme 2. Resection of colorectal cancer by surgery All patients will receive curcumin 1.8 g daily

Sponsors

University Hospitals of Leicester NHS Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Found to have faecal occult blood (FOB) as part of National Colorectal Cancer Screeing Programme or those awaiting resection of known colorectal cancer 2. Over 18 years of age, either sex 3. Using contraception

Exclusion criteria

Exclusion criteria: 1. History in past year of discrete gastric or duodenal ulcer of size greater than 5 mm 2. Inability to return for follow up tests 3. Significant medical or psychiatric problems (including renal, hepatic or haematological dysfunction) 4. Use of any investigational agent within last 3 months 5. History of pelvic radiation 6. Women of child bearing age unless they agree to provide written confirmation that they are using adequate contraception

Design outcomes

Primary

MeasureTime frame
From 30 eligible patients who are compliant in taking all doses have tissue measurement of curcumin greater than or equal to 5 nMol/g tissue, assessed approximately two months after completion of the trial when the colon biopsies will be assayed in the laboratories for curcumin levels. The exact timing of assay will vary depending on the number of samples which will be batched together for assessment.

Secondary

MeasureTime frame
To assess the practicality, acceptability and safety of individuals taking 5 capsules of curcumin (2.25 g total daily dose of curcuminoids, 1.8 g curcumin) daily for 14 days, assessed at 3 weeks from entry to the study.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026