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Renal Cell CarcinomaLiangAHNCT06317207

Evaluation of the Safety of Reoperation for Ipsilateral Recurrent Tumors After Nephron-sparing Partial Nephrectomy

An observational study of Renal Cell Carcinoma and Robotic Surgical Procedures, run by The First Affiliated Hospital of Anhui Medical University.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

To evaluate the safety of reoperation in patients with renal tumors who have ipsilateral tumor recurrence after nephron-sparing partial nephrectomy. Read more about this study

Who is it for?
Any age
How many people
15 participants
Where
No sites listed yet
Study dates
1 Jan 2013to 31 Dec 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: We collected the patients who underwent reoperation for locally rRCC after pNSS in our institution from 2013 to 2023.

Who may be able to join

  • 1. ipsilateral local rRCC (any recurrence in the ipsilateral kidney and retroperitoneum)

Who cannot join

  • With distant metastasis;
  • Lacking essential sugery information.

About this study

Official title: Reoperation for Ipsilateral Local Recurrence Following Prior Nephron-sparing Surgery: Innovative Surgical Insights From a High-volume Urological Center

To evaluate the safety of reoperation in patients with renal tumors who have ipsilateral tumor recurrence after nephron-sparing partial nephrectomy.

Medical subject headings
Carcinoma, Renal Cell

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06317207
Study groupRoleWhat they receive
observation grouppatients who underwent reoperation for locally rRCC after pNSS

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Operation time

    Operation time

    Measured: 1 week

Secondary outcomes (1)
  1. Estimated blood loss

    Estimated blood loss

    Measured: 1 week

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Mar 2024
  2. Study start1 Jan 2013
  3. Primary completion31 Dec 2023
  4. Study completion31 Dec 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Retrospective
Enrolment
15 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06317207
Sponsor's protocol ID
PJ2024-01-44
Other IDs
2019b07030004
Acronym
LiangAH
Status last verified
Mar 2024
First submitted
9 Mar 2024
Last updated
19 Mar 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: All the information we will provide with the publication

Questions about this trial

What is this clinical trial studying?

An observational study of Renal Cell Carcinoma and Robotic Surgical Procedures, run by The First Affiliated Hospital of Anhui Medical University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Mar 2024. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Operation time (time frame: 1 week). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Mar 2024.

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