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ccRCCNCT06791863

Visceral Fat Area as a Prognostic Biomarker in Clear Cell Renal Cell Carcinoma: A Multicenter Study on Postoperative Survival

An observational study of ccRCC, run by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This retrospective study included 1030 patients with clear cell renal cell carcinoma (ccRCC) who underwent radical or partial nephrectomy at Wuhan Union Hospital from 2014 to 2023. Read more about this study

Who is it for?
Any age
Conditions the study is for
ccRCC
Type of treatment
Injection or infusion
How many people
1,030 participants
Where
1 siteChina
Study dates
1 Nov 2014to 30 Sep 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: patients with clear cell renal cell carcinoma (ccRCC) who underwent radical or partial nephrectomy

Who may be able to join

  • primary clear cell renal cell carcinoma confirmed by histopathology;
  • patients≥18 years;
  • availability of preoperative abdominal computed tomography (CT) data;
  • patients with partial or radical nephrectomy.

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

China1 site
  • Wuhan Union Hospital

    Wuhan, Hubei, 430000

Other trials in China

About this study

This retrospective study included 1030 patients with clear cell renal cell carcinoma (ccRCC) who underwent radical or partial nephrectomy at Wuhan Union Hospital from 2014 to 2023.

Conditions
ccRCC

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06791863
Study groupRoleWhat they receive
Cohort 1The group with high area of body compositions (skeletal muscle, subcutaneous fat, subcutaneous fat or total fat)
Cohort 2the group with low area of body compositions (skeletal muscle, subcutaneous fat, subcutaneous fat or total fat)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. overall survival (OS)

    Measured: 5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jan 2025
  2. Study start1 Nov 2014
  3. Primary completion30 Sep 2023
  4. Study completion30 Sep 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
1,030 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06791863
Sponsor's protocol ID
0361-02
Status last verified
Jan 2025
First submitted
19 Jan 2025
Last updated
24 Jan 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of ccRCC, run by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Jan 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

overall survival (OS) (time frame: 5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jan 2025.

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