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6-year Follow-up Data After the Berberine Intervention Trial

S

Shanghai Jiao Tong University School of Medicine

Status

Enrolling

Conditions

Colorectal Adenoma
Colorectal Cancer Control and Prevention
Colorectal Polyps

Treatments

Drug: Placebo
Drug: Berberine Hydrochloride

Study type

Observational

Funder types

Other

Identifiers

NCT06629051
LY2024-232-A

Details and patient eligibility

About

Colorectal cancer (CRC) is a common malignancy of the digestive tract, which constitutes a major public health burden. Almost 90% of CRC cases progress from precursor adenomatous polyps through adenoma-carcinoma sequence. Endoscopic detection and removal of colorectal adenoma (CRA) could reduce the incidence and mortality risk of CRC, but the recurrence rate is still high. Therefore, chemoprevention is quite important, not only solve the urgent public health problem, but also be cost-effective.

In 2020, the investigators published a multicenter, randomized, double-blind, placebo-controlled clinical study (NCT02226185) in the Lancet Gastroenterology & Hepatology. The result concluded that oral BBR for 2 years significantly reduced recurrence after endoscopic removal of CRA (RR 0.77, 95%CI 0.66-0.91; p=0.001). BBR also has a significant preventive effect on all polypoid lesions, including adenomas and serrated lesions (adjusted RR 0.78, 95%CI 0.66-0.91; p=0.002) . Does BBR still have a long-term protective effect on the recurrence of CRA after discontinuation? That's what the investigators concerned.

The present study is performed to observe and compare retrospectively the recurrence rate of CRAs in patients of the original BBR RCT study (NCT02226185) within 6 years after discontinuation of medication, including the overall recurrence rate of traditional adenomas within the first year, 1-3 years, 3-6 years, and the entire follow-up period of 6 years. The aim is to evaluate the long-term efficacy of BBR in preventing recurrence and carcinogenesis after endoscopic resection of CRAs.

Enrollment

891 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: participants who completed the previous berberine intervention study (NCT02226185) Exclusion Criteria: no

Trial design

891 participants in 2 patient groups

berberine
Description:
post-intervention of berberine
Treatment:
Drug: Berberine Hydrochloride
placebo
Description:
post-intervention of placebo tablets
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Central trial contact

Jing-Yuan Fang, Professor

Data sourced from clinicaltrials.gov

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