Kidney Cancer Trial, Recruiting NCT07321197 Sponsor: Tianjin Medical University Second Hospital Condition: Kidney Cancer
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Kidney Cancer Trial, Recruiting

NCT07321197
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 signed a consent form agreeing to take part in the study.
  • People aged 18 or older.
  • People who are being considered for surgery to fully remove a kidney, with or without removal of nearby lymph nodes.
  • People diagnosed with high-risk kidney cancer meeting at least one of the following: cancer that has grown into surrounding tissue or lymph nodes but not spread elsewhere (stage cT3-4); a lymph node visible on scans measuring more than 1cm; cancer that had spread to other parts of the body but was treated and shows no remaining signs of disease; or cancer that has grown into nearby organs on scans. Alternatively, people meeting at least two of these features: cancer growing into the main kidney vein or a large vein leading to the heart; aggressive tumour characteristics under the microscope; a tumour 10cm or larger; or blood in urine and/or local symptoms (confirm with trial site).
  • People whose cancer can be measured on scans according to standard criteria (RECIST v1.1).
  • People who are generally well enough to carry out light activity and care for themselves (ECOG score of 0 or 1).
  • People whose blood, kidney, and liver results are within an acceptable range.
  • People of childbearing potential who agree to use effective contraception throughout the study.

Who may not be able to join:

  • People who have previously had radiotherapy, chemotherapy, major surgery, or targeted drug treatment for kidney cancer.
  • People who currently have another active cancer (except certain well-controlled cancers not expected to affect survival within two years).
  • People whose medical team has determined that a partial kidney removal or tumour ablation procedure would be more appropriate.
  • People whose scans suggest that nearby lymph nodes cannot be surgically removed.
  • People with certain hereditary kidney cancer conditions (confirm with trial site).
  • People diagnosed with any other active cancer within the past five years.
  • People with an active or past autoimmune disease (a condition where the immune system attacks the body).
  • People who have taken immune-suppressing medications within two weeks before joining the study.
  • People with poorly controlled heart conditions or significant related symptoms.
  • People with blood clotting problems or a tendency to bleed.
  • People with active digestive conditions that carry a risk of bleeding or perforation.
  • People with a history of significant bleeding or serious blood clot events within certain timeframes (confirm with trial site).
  • People with a current infection or an unexplained fever above 38.5°C.
  • People who had an abdominal fistula, bowel perforation, or abscess within the four weeks before joining.
  • People with a history of lung scarring, interstitial lung disease, or severely reduced lung function.
  • People with a known immune deficiency condition or active hepatitis.
  • People who have taken part in another clinical trial within the past month.
  • People with a known history of drug or alcohol addiction.
  • People who are unable or unwilling to cover any required out-of-pocket costs for examinations and treatment.
  • People with any other condition that the trial doctor believes could affect their safety or the conduct of the study.

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 20 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

Principal Investigator: Changyi Quan, MD, Tianjin Medical University Second Hospital

Phone: +86 88328607

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
Tianjin Medical University Second Hospital
Registry
ClinicalTrials.gov
Start date
1 September 2025
Est. completion
30 September 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Disease-Free Survival (DFS); Overall Survival (OS); Incidence and Severity of Postoperative Complications (Perioperative Safety)

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: 20 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