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NCT Number: NCT03602092

Observational Registry Data on GIST Patients

This is a longitudinal, multi-center, registry study, collecting data via a web-based portal in patients with GIST (Gastrointestinal Stromal Tumor) from hospitals in Taiwan.

Recruiting

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Yu wei-lan

Taipei, 10048, Taiwan

Location status: Recruiting

Location contact

Hui-Jen Tsai

PRINCIPAL_INVESTIGATOR

Wei-lan Yu, College

CONTACT

[email protected]

+886-2-23123456 ext. 67658

About this study

Research question and objectives:

This study is to collect and describe real-world data for Taiwanese GIST on:

  • Prevalence and demographic characteristics of Taiwanese GIST
  • Treatment pattern of GIST therapies
  • Bio-marker and/or gene expression characteristics of Taiwanese GIST
  • Treatment outcome of TKI therapies, including recurrence-free, progression-free and overall survival
  • Safety profile for TKI therapies

Study design: Retrospective and prospective observational cohort study Population: Taiwan GIST patients during 01 January 2010 to 31 December 2020 Data sources: Medical records and investigator-established data bank Study size: Data from up to 3,000 eligible subjects will be collected Data analysis: Descriptive statistics for longitudinally assess nationwide trends on current and evolving diagnostic, treatment, and outcome measures in the GIST population and estimate the prevalence of GIST in Taiwan.

Milestones: Interim report before 31 December 2018 and final study report before 30 June 2026.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients diagnosed with Gastrointestinal Stromal Tumor
  • ≥20 years old
  • Histology-confirmed GIST between 01 January 2010 and 31 December 2020.
  • Patient with prospective data collection: Willing to provide singed inform-consent as per local regulatory requirements.

Exclusion criteria

  • Inability and unwillingness to give informed consent if required by site ethic committee.
  • Patient that is unlikely candidate to obtain long-term follow-up information for reasons of unavailability or with severe concomitant illnesses per investigator judgement

Treatment and study plan

observation

Other

This is a longitudinal, multi-center, registry study, collecting data via a web-based portal in patients with GIST (Gastrointestinal Stromal Tumor) from hospitals in Taiwan.

Primary outcomes

  1. To establish the database for GIST

    Time frame: From date of registration to 31 December 2025

    By register the clinical presentation, diagnostic, stage, treatment and clinical outcome of GIST patients.

Study contacts

Contact information is provided by the study sponsor or research team.

Hui-Jen Tsai, M.D

CONTACT

[email protected]

886-06-2083427 ext. 65149

Wei-Lan Yu, MSN

CONTACT

[email protected]

886-2-3123456 ext. 67658

Sponsors and collaborators

Lead sponsor

National Health Research Institutes, Taiwan

Other

Collaborators

  • Chang Gung Memorial Hospital
  • Changhua Christian Hospital
  • China Medical University Hospital
  • Kaohsiung Medical University
  • National Cheng-Kung University Hospital
  • National Taiwan University Hospital
  • Taichung Veterans General Hospital
  • Taipei Veterans General Hospital, Taiwan

Registry information

Official study title

The Observational Registry: Nationwide Data Collection on Gastrointestinal Stromal Tumors (GISTs) Patients (Taiwan GISTs Registry)

Important dates

Study start
2018
Primary completion
2025
Study completion
2025
First posted
Jul 26, 2018
Registry last updated
May 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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