# Frequency, Clinical Phenotype and Genetic Analysis of Heritable Kidney Cancer Syndromes

> **NCT05534854** · — · UNKNOWN · sponsor: **RenJi Hospital** · enrollment: 500 (estimated)

## Conditions studied

- Renal Tumor Histology
- Kidney Cancer
- Renal Cell Carcinoma
- Familial Renal Cancer
- HLRCC
- VHL Syndrome
- BAP1 Tumor Predisposition Syndrome
- FLCN Gene Mutation
- ALK Gene Mutation
- FH Gene Mutation
- Birt-Hogg-Dube Syndrome
- MET Gene Mutation
- Cutaneous Leiomyoma
- Cutaneous Leiomyomata With Uterine Leiomyomata

## Interventions

- **GENETIC:** Gene test

## Key facts

- **NCT ID:** NCT05534854
- **Lead sponsor:** RenJi Hospital
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2022-10-01
- **Primary completion:** 2025-08-01
- **Final completion:** 2025-08-01
- **Target enrollment:** 500 (ESTIMATED)
- **Last updated:** 2023-08-31

## Collaborators

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## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05534854

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05534854, "Frequency, Clinical Phenotype and Genetic Analysis of Heritable Kidney Cancer Syndromes". Retrieved via AI Analytics 2026-07-20 from https://api.ai-analytics.org/clinical/NCT05534854. Licensed CC0.

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