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Tenosynovial Giant Cell Tumors (TGCT) Observational Platform Project (TOP)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02948088
Recruitment Status : Active, not recruiting
First Posted : October 28, 2016
Last Update Posted : January 20, 2021
Sponsor:
Collaborator:
SSS International Clinical Research GmbH
Information provided by (Responsible Party):
Daiichi Sankyo, Inc.

Tracking Information
First Submitted Date October 24, 2016
First Posted Date October 28, 2016
Last Update Posted Date January 20, 2021
Study Start Date November 2016
Estimated Primary Completion Date April 2021   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: October 26, 2016)
  • Percentage of participants with disease status reported as one of the categorical descriptions at Baseline [ Time Frame: at Baseline ]
    Only patients with disease status reported as one of the five categorical descriptions below are included in this observation:
    • fully active/able to carry on all pre-disease activities without restriction (0)
    • restricted in physically strenuous activity, but ambulatory/able to carry out light or sedentary work (1)
    • ambulatory (greater than [>] 50 percentage [%] of waking hours [h]), capable of all self care, but unable to carry out any work activities (2)
    • capable of only limited self care, confined to bed/chair >50% of waking hours (3)
    • completely disabled, cannot carry on any selfcare, totally confined to bed or chair (4)
    • dead (5)
  • Percentage of participants with disease status reported as one of the categorical descriptions at 12 Months [ Time Frame: at 12 Months ]
    Only patients with disease status reported as one of the five categorical descriptions below are included in this observation:
    • fully active/able to carry on all pre-disease activities without restriction (0)
    • restricted in physically strenuous activity, but ambulatory/able to carry out light or sedentary work (1)
    • ambulatory (greater than [>] 50 percentage [%] of waking hours [h]), capable of all self care, but unable to carry out any work activities (2)
    • capable of only limited self care, confined to bed/chair >50% of waking hours (3)
    • completely disabled, cannot carry on any selfcare, totally confined to bed or chair (4)
    • dead (5)
  • Percentage of participants with disease status reported as one of the categorical descriptions at 24 Months [ Time Frame: at 24 Months ]
    Only patients with disease status reported as one of the five categorical descriptions below are included in this observation:
    • fully active/able to carry on all pre-disease activities without restriction (0)
    • restricted in physically strenuous activity, but ambulatory/able to carry out light or sedentary work (1)
    • ambulatory (greater than [>] 50 percentage [%] of waking hours [h]), capable of all self care, but unable to carry out any work activities (2)
    • capable of only limited self care, confined to bed/chair >50% of waking hours (3)
    • completely disabled, cannot carry on any selfcare, totally confined to bed or chair (4)
    • dead (5)
Original Primary Outcome Measures Same as current
Change History
Current Secondary Outcome Measures
 (submitted: October 26, 2016)
  • Mean Number of Referrals or Specialist Visits to Assess the Health Resource Utilization in Patients with Diffuse TGCT through 24 Months [ Time Frame: at Baseline, 12 Months, 24 Months ]
    Categories: Baseline, 12 Months, 24 Months
  • Mean Brief Pain Inventory (BPI) Average Interference Score From Baseline through 24 Months [ Time Frame: Baseline, 6, 12, 18 and 24 months ]
    The BPI short form is a 5 minutes self administered questionnaire that assesses severity of pain, impact of pain on daily function, location of pain, pain medications and amount of pain relief in the past 24 hours or the past week. The change from baseline at each time point reflects the month X value minus the baseline value. The BPI average interference score ranges from 0 (pain does not interfere) to 10 (pain completely interferes). Categories (scores on a scale): at Baseline, at Month 6, at Month 12, at Month 18 and at Month 24
  • Mean Worst Stiffness Score from Baseline through 24 Months [ Time Frame: Baseline, 6, 12, 18 and 24 months ]
    The Worst Stiffness numerical rating scale (NRS) is a one-item self-administered questionnaire assessing the "worst" stiffness in the last 24 hours. The NRS for this item ranges from 0 ("no stiffness") to 10 ("stiffness as bad as you can imagine"). Categories (scores on a scale): at Baseline, at Month 6, at Month 12, at Month 18 and at Month 24
  • Mean PROMIS Physical Function Score from Baseline through 24 Months [ Time Frame: Baseline, 6, 12, 18 and 24 months ]
    PROMIS® (Patient-Reported Outcomes Measurement Information System) is a set of person-centered measures, developed by the US Department of Health and Human Services, that evaluates and monitors physical, mental, and social health. Physical function items relevant to the assessment of lower and upper limb function are to be selected from the PROMIS physical function item bank. Items assessing lower limb function will be administered to subjects with lower extremity tumors, and items assessing upper limb function will be administered to subjects with upper extremity tumors. The results from both sets of items will be combined and analyzed together. Categories (scores on a scale): at Baseline, at Month 6, at Month 12, at Month 18 and at Month 24
  • Mean Scores on the EuroQol Questionnaire (EQ) of 5 Dimensions (5D) on a Standardized 5-level (5L) Descriptive Health Status Scale (EQ-5D-5L), from Baseline through 24 Months [ Time Frame: Baseline, 6, 12, 18 and 24 months ]
    The EQ-5D questionnaire is made up for two components; health state description and evaluation. The EQ-5D-5L is the health state description for measuring health status. The descriptive system comprises the 5 dimensions of mobility, self care, usual activities, pain/discomfort, and anxiety/depression. The participants self-rate each dimension on a 5-point, categorical scale: no problems, slight problems, moderate problems, severe problems, and extreme problems. Categories (scores on a scale): at Baseline, at Month 6, at Month 12, at Month 18 and at Month 24
  • Mean Scores on the EQ-5D Visual Analogue Scale (EQ VAS) Evaluation, from Baseline through 24 Months [ Time Frame: Baseline, 6, 12, 18 and 24 months ]
    The EQ-5D questionnaire is made up for two components; health state description and evaluation. The EQ VAS is the evaluation that records the respondent's self-rated health on a 20 cm vertical, VAS with ends labeled "the best health you can imagine" and "the worst health you can imagine". Categories (scores on a scale): at Baseline, at Month 6, at Month 12, at Month 18 and at Month 24
Original Secondary Outcome Measures Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Tenosynovial Giant Cell Tumors (TGCT) Observational Platform Project
Official Title A Disease Registry for Patients With Tenosynovial Giant Cell Tumors (TGCT), Also Known as Pigmented Villonodular Synovitis (PVNS) and Giant Cell Tumor of the Tendon Sheath (GCT-TS)
Brief Summary

TGCT is a rare disease that is difficult to manage, surgical resection is the primary treatment currently available. To date no disease registry exists and there is little data available detailing the management of patients with diffuse TGCT, the burden of diffuse TGCT for patients (including pain, joint stiffness, swelling, reduced mobility and quality of life) or the economic impact of diffuse TGCT.

This study aims to collect data by an observational disease registry involving no intervention to the patient or changes to investigators treatment decisions.

Detailed Description

GCT is a rare, benign, but potentially locally aggressive and recurrent disease. Treatment pattern and treatment initiation, continuation or changes are solely at the discretion of the physician and the patient.

There will be no attempt to influence the prescribing patterns of any individual treating physician. All medication will be prescribed in the usual standard of care and will not be provided by the study sponsor.

Participation in the study will in no way influence payment or reimbursement for any treatment received by patients during the study.

It is the responsibility of the investigator and his study staff to enter all relevant patient data required for this registry in the electronic Case Report Form (eCRF) and in the patients' medical records.

Approximately 15 sites from up to 6 European Countries (France, Germany, Italy, The Netherlands, Spain and United Kingdom) and 4 sites from the US are planned to participate. The sites will be specialized sites that treat diffuse TGCT regularly.

Study Type Observational [Patient Registry]
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration 24 Months
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population Patients with diffuse TGCT
Condition Giant Cell Tumors
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Active, not recruiting
Estimated Enrollment
 (submitted: October 12, 2017)
200
Original Estimated Enrollment
 (submitted: October 26, 2016)
100
Estimated Study Completion Date June 2021
Estimated Primary Completion Date April 2021   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Written informed consent for participation in the study (ICF)
  • Patients with diffuse TGCT (diagnosed histologically) confirmed naïve or recurrent case

Exclusion Criteria:

  • None
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Austria,   France,   Germany,   Italy,   Netherlands,   Spain,   United Kingdom,   United States
Removed Location Countries  
 
Administrative Information
NCT Number NCT02948088
Other Study ID Numbers DS-ONC-01-15-EU
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement
Plan to Share IPD: Yes
Plan Description: De-identified individual participant data (IPD) and applicable supporting clinical trial documents may be available upon request at https://vivli.org/. In cases where clinical trial data and supporting documents are provided pursuant to our company policies and procedures, Daiichi Sankyo will continue to protect the privacy of our clinical trial participants. Details on data sharing criteria and the procedure for requesting access can be found at this web address: https://vivli.org/ourmember/daiichi-sankyo/
Supporting Materials: Study Protocol
Supporting Materials: Statistical Analysis Plan (SAP)
Supporting Materials: Clinical Study Report (CSR)
Time Frame: Studies for which the medicine and indication have received European Union (EU) and United States (US), and/or Japan (JP) marketing approval on or after 01 January 2014 or by the US or EU or JP Health Authorities when regulatory submissions in all regions are not planned and after the primary study results have been accepted for publication.
Access Criteria: Formal request from qualified scientific and medical researchers on IPD and clinical study documents from clinical trials supporting products submitted and licensed in the United States, the European Union and/or Japan from 01 January 2014 and beyond for the purpose of conducting legitimate research. This must be consistent with the principle of safeguarding study participants' privacy and consistent with provision of informed consent.
URL: https://vivli.org/ourmember/daiichi-sankyo/
Responsible Party Daiichi Sankyo, Inc.
Study Sponsor Daiichi Sankyo, Inc.
Collaborators SSS International Clinical Research GmbH
Investigators
Study Director: Global Clinical Leader Daiichi Sankyo, Inc.
PRS Account Daiichi Sankyo, Inc.
Verification Date January 2021