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NCT06167863
Retrospective Analysis of the Correlation Between Imaging Features and Pathology, Prognosis in Renal Tumors
trial testing radiomics in Radiomics in 1,000 participants. Completed in 31 October 2023.
31 October 2023
Quick facts
| Lead sponsor | Zhen Li |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 1,000 |
| Start date | 31 August 2023 |
| Primary completion | 31 October 2023 |
| Estimated completion | 31 October 2023 |
| Sites | 1 location across China |
Drugs / interventions tested
- radiomics
Conditions studied
- Radiomics — all drugs for Radiomics →
- Deep Learning — all drugs for Deep Learning →
- Artificial Intelligence — all drugs for Artificial Intelligence →
- Body Composition — all drugs for Body Composition →
Sponsor
Zhen Li — full company profile →
Who can join
Eligibility, any sex, with Radiomics or Deep Learning. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Renal cell carcinoma (RCC) is the most common malignant tumor in the kidney with a high mortality rate. Traditional imaging techniques are limited in capturing the internal heterogeneity of the tumor. Radiomics provides internal features of lesions for precise diagnosis, prognosis prediction, and personalized treatment planning. Early and accurate diagnosis of renal tumors is crucial, but it's challenging due to morphological and pathological overlap between benign and malignant lesions. The accurate diagnosis of RCC, especially for small tumors, remains a significant challenge. Recent studies have shown a relationship between body composition, obesity, and renal tumors. Common indicators like body weight and BMI fail to reflect body composition accurately. Research on the role of body composition, including adipose tissue, in tumor pathology could improve clinical diagnosis and treatment planning.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Incremental value of automatically segmented perirenal adipose tissue for pathological grading of clear cell renal cell carcinoma: a multicenter cohort study.
Li S, Zhou Z, Gao M, Liao Z, et al · · 2024 · cited 13× · PMID 38573065 · DOI 10.1097/js9.0000000000001358
Verify or expand the search:
- PubMed search for NCT06167863
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Trials testing the same drug.
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- NCT04955522 — Multimodal Imaging Analysis of Spinal Tumors · completed
- NCT03872362 — Radiomics Multifactorial Biomarker for Pulmonary Nodules · completed
- NCT03221049 — Radiomics for Diagnosing Liver Diseases and Evaluating Progression · unknown
Other recruiting trials for Radiomics
Currently open trials in the same condition.
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Other Zhen Li trials
Trials by the same sponsor.
- NCT07001917 — To Explore the Value of Magnetic Resonance Imaging in Noninvasive Quantitative Evaluation of Graft Function After Simult · enrolling by invitation
- NCT06946771 — Exploring the Correlation Between MRI Image Characteristics and Diagnosis, Pathology and Prognosis in Patients With Pros · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06167863 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Zhen Li
- Last refreshed: 13 December 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06167863.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing