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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorShanghai Jiao Tong University School of Medicine

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

We included 895 participants who completed the previous berberine intervention study (NCT02226185), including 432 participants in the BBR group and 463 participants in the placebo group.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Berberine Hydrochloride

    Drug

    post-intervention of berberine

  • Placebo

    Drug

    Looks the same as berberine

Treatment groups

891 Participants
are divided into 2 treatment groups
Group A: berberine1 intervention
Group B: placebo1 intervention

Trial outcomes

Primary outcomes

1

The recurrence rates of traditional colorectal adenomas within the follow-up period of 6 years

The cumulative recurrence rate of CRAs within the entire follow-up period of 6 years. The recurrence rates of CRAs within the first year, 1-3 years, 3-6 years. The number, size and location of all adenomas are assessed.

Time frame
6 years, 1-3 years, 3-6 years

Secondary outcomes

1

The incidence rates of hyperplastic polyps and serrated adenomas within 6 years after discontinuation of medication

The recurrence rates within the first year, 1-3 years, 3-6 years, and the entire follow-up period of 6 years.

Time frame
6 years, 1-3 years, 3-6 years
2

Subgroup analyses

For patients with advanced CRA or high-risk adenomas (including advanced CRA and multiple adenomas≥3),the recurrence rates of CRAs and polyps are further evaluated.

Time frame
6 years, 1-3 years, 3-6 years

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Shanghai Jiao Tong University School of Medicine

Lead sponsor

Seventh Medical Center of PLA Army General Hospital

Collaborator

Zhongshan Hospital Xiamen University

Collaborator

Nanfang Hospital, Southern Medical University

Collaborator

The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

Collaborator

Tianjin Medical University General Hospital

Collaborator

the Tenth People's Hospital affiliated to Tongji University

Collaborator