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Study on Clinical Features, Treatment Mode and Survival of Bone and Soft Tissue Tumors

Single-center Real World Prospective Observational Study of Clinical Features, Treatment Patterns, and Survival of Bone and Soft Tissue Tumors

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05468970
Enrollment
6000
Registered
2022-07-21
Start date
2022-08-03
Completion date
2032-07-31
Last updated
2023-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone and Soft Tissue Tumors, Clinical Features

Brief summary

It is planned to prospectively collect, collate and report real-world clinical data of BSTS patients treated in our hospital in the next ten years to evaluate the changes in clinical characteristics, treatment patterns and survival information of these patients, in order to provide reference for clinical treatment and research of this type of tumor.

Detailed description

It is planned to prospectively collect, collate and report real-world clinical data of BSTS patients treated in our hospital in the next ten years to evaluate the changes in clinical characteristics, treatment patterns and survival information of these patients, in order to provide reference for clinical treatment and research of this type of tumor. This study is a single-center, prospective, real-world observational study that plans to enroll all eligible patients. Basic information, treatment methods, and prognostic information of these patients were collected.

Interventions

OTHERNO Intervention

NO Intervention

Sponsors

Henan Cancer Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

All ages, male and female. The pathological diagnosis of BSTS in our hospital was a subtype. Has received at least one hospitalization in this hospital. The target lesions could be evaluated according to the efficacy evaluation criteria of solid tumor (RECIST; Version 1.1) Measure diameter changes.

Exclusion criteria

No definite pathology.

Design outcomes

Primary

MeasureTime frameDescription
6/5000 Progression-free survivalUp to approximately 48monthsThe time from the first use of the treatment to the observation of disease progression
Overall survivalUp to approximately 120monthsPathologically confirmed events leading to death

Countries

China

Contacts

Primary ContactWang Jiaqiang, Dr.
wjqwtj@126.com13592413731

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026