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NCT02346435Recruiting

The Delayed Intervention and Surveillance for Small Renal Masses (DISSRM) Registry

Source: ClinicalTrials.gov · Last updated 5 Mar 2026

Brief summary (registry, in English)

Retrospective studies indicate that active surveillance for clinically localized, small renal masses (cT1a, \<=4cm) is safe. It is our hypothesis that active surveillance is safe and efficacious when compared prospectively to patients undergoing immediate intervention for their small renal mass.

Status (registry)
Recruiting
Study type
Observational
Enrollment
600 (estimated)
First submitted
6 Jun 2014
Start date
Jan 2009
Primary completion date
Jan 2028
Lead sponsor
Abramson Cancer Center at Penn Medicine
NCT number
NCT02346435

What you commit to

  • Study type: Observational
  • Planned participants: 600
  • From Jan 2009 to the primary completion date, Jan 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Cannot have suspicion of metastases to the kidney if any other malignancy diagnosed within two years of study entry.

Who the study is looking for

  • Must have a solid, enhancing renal mass ≤4cm at its greatest dimension found on incidental scanning in the last 6 months.
  • Age ≥ 18 and able to read, understand and sign informed consent.
  • Must be willing to adhere to the treatment algorithm and time constraints therein.

Age in the registry: 18 years to 100 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Johns Hopkins Hospital
Coordinator of this site? Confirm its status
BaltimoreUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.