Kidney Cancer Trial, Recruiting NCT05917106 Sponsor: Jinling Hospital, China Condition: Kidney Cancer
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Kidney Cancer Trial, Recruiting

NCT05917106
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have recently been diagnosed with kidney cancer (renal cell carcinoma) for the first time
  • People who have not yet received any treatment for their cancer
  • People who are willing to have surgery to remove the affected kidney or tumour
  • People who have signed a written consent form agreeing to take part
  • People whose general health and ability to carry out daily activities meets a specific standard (rated 0 or 1 on a medical scale, meaning fully active or able to carry out light work)
  • People who are able and willing to attend follow-up appointments and complete the required procedures during the trial

Who may not be able to join:

  • People who have had, or currently have, another type of cancer
  • People who have previously received any cancer treatment
  • People who are known or suspected to have an active autoimmune disease (a condition where the immune system attacks the body)
  • People who are unable to give informed consent due to a medical or mental health condition
  • People who have heart-related symptoms or heart conditions that are not well managed
  • People who the trial doctors consider to be unsuitable for the study for any reason (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 15720625951

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Jinling Hospital, China
Registry
ClinicalTrials.gov
Start date
26 December 2022
Est. completion
1 June 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

To explore the predictive effect of ctDNA methylomics on the prognosis and medication guidance of renal carcinoma.; To explore the advance time of ctDNA methylomics in monitoring postoperative recurrence of renal cancer compared with imaging.; The molecular mechanism of renal cancer recurrence was analyzed with baseline tissue and circulating methylation profiles.; A renal cancer recurrence risk model was established based on clinical information, molecular risk factors and ctDNA methylomics

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov