findmyKOL
Clinical trialNCT05534854UnknownObservational

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

SponsorRenJi HospitalEnrollment500ALK Gene MutationBAP1 Tumor Predisposition SyndromeBirt-Hogg-Dube SyndromeCutaneous LeiomyomaCutaneous Leiomyomata With Uterine LeiomyomataFH Gene Mutation+8 more conditions
View the registry record on ClinicalTrials.gov

Summary

The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

1 registered facility, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

China
  • Ethics Committee of Shanghai Renji Hospital

    Shanghai, Shanghai Municipality, China

    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
1 Oct 2022
Primary completion
1 Aug 2025
Completion
1 Aug 2025
Last update posted
31 Aug 2023
Registered enrollment
500
Registry id
NCT05534854

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.