NCT03400514

Brief Summary

At present, Watson for Oncology has been applied in 14 countries worldwide, including China, the United States, Holland, Thailand, India, Korea, Poland, Slovakia and Bangladesh. In a double-blind study involving 362 patients in India, treatment recommendations from Watson for Oncology (WFO) performed a high degree of consistency with their multidisciplinary tumor board. The investigators would recruit cancer patients diagnosed as lung cancer, breast cancer, gastric cancer, colon cancer, rectal cancer,cervical cancer or ovarian cancer according to the criteria of Watson for Oncology ,using the updated version of Watson for Oncology to explore the concordance of therapeutic regimen between WFO and physicians in the Affiliated Hospital of Qingdao University.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
350

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Apr 2017

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 12, 2017

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

December 21, 2017

Completed
27 days until next milestone

First Posted

Study publicly available on registry

January 17, 2018

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2018

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2019

Completed
Last Updated

January 18, 2018

Status Verified

January 1, 2018

Enrollment Period

1.7 years

First QC Date

December 21, 2017

Last Update Submit

January 17, 2018

Conditions

Keywords

Artificial intelligenceconcordance

Outcome Measures

Primary Outcomes (1)

  • concordance

    the concordance of therapeutic regimen between WFO and physicians in the Affiliated Hospital of Qingdao University

    Day 0

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

cancer patients from outpatient and inpatient in our hospital

You may qualify if:

  • a histology of lung cancer,breast cancer,gastric cancer, colon cancer, rectal cancer,cervical cancer and ovarian cancer
  • had no prior systemic therapy and need neoadjuvant/adjuvant or metastatic therapy
  • had prior neoadjuvant therapy, adjuvant therapy and/or surgery and are now metastatic
  • have had prior surgery and now need adjuvant therapy
  • seeking an additional therapy whose cancer has progressed beyond its initial metastatic therapy (second line)

You may not qualify if:

  • not have confirmed diagnoses of invasive cancer
  • under 18 years of age
  • pregnant
  • with multiple concurrent primary cancers or a local recurrence or a new primary at the same site of a previously treated cancer

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Affiliated Hospital of Qingdao University

Qingdao, Shandong, China

RECRUITING

Related Publications (1)

  • Zhou N, Zhang CT, Lv HY, Hao CX, Li TJ, Zhu JJ, Zhu H, Jiang M, Liu KW, Hou HL, Liu D, Li AQ, Zhang GQ, Tian ZB, Zhang XC. Concordance Study Between IBM Watson for Oncology and Clinical Practice for Patients with Cancer in China. Oncologist. 2019 Jun;24(6):812-819. doi: 10.1634/theoncologist.2018-0255. Epub 2018 Sep 4.

MeSH Terms

Conditions

Neoplasms

Study Officials

  • Xiaochun Zhang

    The Affiliated Hospital of Qingdao University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

December 21, 2017

First Posted

January 17, 2018

Study Start

April 12, 2017

Primary Completion

December 31, 2018

Study Completion

January 31, 2019

Last Updated

January 18, 2018

Record last verified: 2018-01

Locations