search
Back to results

Chemoprevention of Esophageal Squamous Cell Carcinoma (ESCC) With Aspirin and Tea Polyphenols (CREAT)

Primary Purpose

Carcinoma, Squamous Cell

Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Aspirin
Tea Polyphenols
Sponsored by
Beijing Friendship Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Carcinoma, Squamous Cell focused on measuring Aspirin, polyphenols, Chemoprevention

Eligibility Criteria

40 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. age 40 to 60 years;
  2. Lugol's chromoendoscopy showing at least one USL 1 cm or larger containing mild to moderate dysplasia and chronic inflammation;
  3. subject neither pregnant nor intending to become pregnant during the study.

Exclusion Criteria:

  1. current non-steroidal anti-inflammatory drugs (NSAID) therapy;
  2. major intercurrent illness;
  3. pregnancy;
  4. invasive carcinoma;
  5. any condition that could be worsened by aspirin or tea polyphenols.

Sites / Locations

  • Beijing Friendship Hospital Capital Medical University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Aspirin

Tea Polyphenols

Control

Arm Description

Outcomes

Primary Outcome Measures

occurrence of high grade dysplasia and invasive ESCC

Secondary Outcome Measures

the mortality of the participants
Number of participants with adverse events.
occurrence of high grade dysplasia and invasive ESCC

Full Information

First Posted
December 15, 2011
Last Updated
December 17, 2011
Sponsor
Beijing Friendship Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT01496521
Brief Title
Chemoprevention of Esophageal Squamous Cell Carcinoma (ESCC) With Aspirin and Tea Polyphenols
Acronym
CREAT
Official Title
Chemoprevention of Esophageal Squamous Cell Carcinoma With Aspirin and Tea Polyphenols: a Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2011
Overall Recruitment Status
Unknown status
Study Start Date
January 2012 (undefined)
Primary Completion Date
June 2012 (Anticipated)
Study Completion Date
January 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beijing Friendship Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Evidence from laboratory studies suggests that aspirin and tea polyphenols may have an antineoplastic effect in esophageal squamous cell carcinoma (ESCC). To assess the safety and efficacy of aspirin and tea polyphenols for preventing ESCC, the investigators designed this double-blind, randomized controlled clinical trial. Research project is planned to recruit 10,000 participants with the ages of 40-60 years in Fengfeng city, Hebei province, China, which has been known as a high incidence region of ESCC. All the participants receive endoscopic examination. Lugol's chromoendoscopy is used to identify esophageal unstained lesions (USLs). The location and size of each USL will be recorded followed by collecting biopsy samples from each USL. Participants with USL are randomly assigned to receive 100 mg/d of aspirin (n=200), 100 mg/d of tea polyphenols (n=200), or placebo (n=200) for six months. Follow-up consists of 2 endoscopic surveillance cycles (the first interval will be at six months and the second at 3 or 5 years later). The primary outcome measure was occurrence of high grade dysplasia and invasive ESCC. Secondary outcome was the mortality of the participants and adverse events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinoma, Squamous Cell
Keywords
Aspirin, polyphenols, Chemoprevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Aspirin
Arm Type
Experimental
Arm Title
Tea Polyphenols
Arm Type
Experimental
Arm Title
Control
Arm Type
No Intervention
Intervention Type
Drug
Intervention Name(s)
Aspirin
Intervention Description
100mg qd for 6 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Tea Polyphenols
Intervention Description
300mg bid for 6 months.
Primary Outcome Measure Information:
Title
occurrence of high grade dysplasia and invasive ESCC
Time Frame
at six months
Secondary Outcome Measure Information:
Title
the mortality of the participants
Time Frame
The first interval will be at six months and the second at 3 or 5 years later.
Title
Number of participants with adverse events.
Time Frame
The first interval will be at six months and the second at 3 or 5 years later.
Title
occurrence of high grade dysplasia and invasive ESCC
Time Frame
at 3 or 5 years later

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: age 40 to 60 years; Lugol's chromoendoscopy showing at least one USL 1 cm or larger containing mild to moderate dysplasia and chronic inflammation; subject neither pregnant nor intending to become pregnant during the study. Exclusion Criteria: current non-steroidal anti-inflammatory drugs (NSAID) therapy; major intercurrent illness; pregnancy; invasive carcinoma; any condition that could be worsened by aspirin or tea polyphenols.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shu-Tian Zhang, MD
Phone
+86 010 63138067
Email
drzstbj@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shu-Tian Zhang, MD
Organizational Affiliation
Beijing Friendship Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beijing Friendship Hospital Capital Medical University
City
Beijing
ZIP/Postal Code
100050
Country
China

12. IPD Sharing Statement

Learn more about this trial

Chemoprevention of Esophageal Squamous Cell Carcinoma (ESCC) With Aspirin and Tea Polyphenols

We'll reach out to this number within 24 hrs