| Recruitment status | Enrolling by invitation |
| Unique ID issued by UMIN | UMIN000028133 |
| Receipt No. | R000032168 |
| Scientific Title | Clinical study for Robot-assisted partial nephrectomy with da Vinci Si |
| Date of disclosure of the study information | 2017/08/01 |
| Last modified on | 2019/08/14 (Ver. 3) |
| Basic information | ||
| Public title | Clinical study for Robot-assisted partial nephrectomy with da Vinci Si | |
| Acronym | Clinical study for Robot-assisted partial nephrectomy | |
| Scientific Title | Clinical study for Robot-assisted partial nephrectomy with da Vinci Si | |
| Scientific Title:Acronym | Clinical study for Robot-assisted partial nephrectomy | |
| Region |
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| Condition | ||
| Condition | Renal Cell Carcinoma | |
| Classification by specialty |
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| Classification by malignancy | Malignancy | |
| Genomic information | NO | |
| Objectives | |
| Narrative objectives1 | We examine the effectiveness and safety of Robot-ssited partial nephrectomy using daVinci Si system. |
| Basic objectives2 | Safety,Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | |
| Assessment | |
| Primary outcomes | intra-and postoperative complications and its contents |
| Key secondary outcomes | Time of general anesthesia, operation time, bleeding, renal ischemic time, frequency of postoperative analgesic use, postoperative hospitalization period, perioperative renal function (before surgery (pre-operative surgery 12 weeks before),the day before surgery, on the day of the surgery, the day after surgery, the surgery three days after, the surgery six days later, after one month, three months after surgery)serum creatinine, eGFR), and before surgery (pre-operative surgery 12 weeks before), the day of one month, three months after surgery of renal scintigraphy), pathology findings |
| Base | |
| Study type | Interventional |
| Study design | |
| Basic design | Single arm |
| Randomization | Non-randomized |
| Randomization unit | |
| Blinding | Open -no one is blinded |
| Control | Self control |
| Stratification | |
| Dynamic allocation | |
| Institution consideration | |
| Blocking | |
| Concealment | |
| Intervention | |||
| No. of arms | 1 | ||
| Purpose of intervention | Treatment | ||
| Type of intervention |
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| Interventions/Control_1 | Diagnosed with renal cell carcinoma and the clinical stage T1a (tumors less than 4 cm) N0M0 or T1b (diameter 4 cm to 7 cm), solitary tumors should be performed robot-assited partial nephrectomy under da Vinci SI. | ||
| Interventions/Control_2 | |||
| Interventions/Control_3 | |||
| Interventions/Control_4 | |||
| Interventions/Control_5 | |||
| Interventions/Control_6 | |||
| Interventions/Control_7 | |||
| Interventions/Control_8 | |||
| Interventions/Control_9 | |||
| Interventions/Control_10 | |||
| Eligibility | ||||
| Age-lower limit |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | 1. diagnosed with renal cell carcinoma and the clinical stage T1a (tumors less than 4 cm) N0M0 or T1b (diameter 4 cm to 7 cm), solitary tumors allows partial resection.
2. age of 20 years or more. 3. written informed consent obtained from the individual persons. |
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| Key exclusion criteria | 1. the patient seems to be difficult to surgery due to previous surgery.
2. activity of heavy multiple cancer among patients. 3.6 months undergoing treatment for kidney cancer. 4. patients with possible discontinuation of anticoagulants. 5. patients requiring blood transfusion anemia or tendency of bleeding. 6. morbid obesity (BMI35 or higher) 7. kidney transplantation history. 8. dialysis patients. 9. pregnant women or pregnant or lactating women 10. patients with a mental illness or psychiatric symptoms. 11. patients have serious complications (angina pectoris, myocardial infarction, serious arrhythmias, uncontrolled diabetes, malignant hypertension, etc.), surgical treatment is difficult. 12. patients who have renal dysfunction (serum creatinine values:1.5mg/dl more), liver function (AST, ALT:100IU/l). 13. patients with bacterial infections require treatment. 14. patients with interstitial Pneumonitis or pulmonary fibrosis. 15. patients with severe drug hypersensitivity, drug allergies. 16. patients with under 20 years old. 17. patient deemed unfit for this protocol. |
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| Target sample size | 10 | |||
| Research contact person | |||||||
| Name of lead principal investigator |
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| Organization | Jichi Medical University, Saitama Medical Center | ||||||
| Division name | Department of Urology | ||||||
| Zip code | 3308503 | ||||||
| Address | 1-847, Amanuma-cho, Omiya-ku, Saitama City, Saitama, Japan | ||||||
| TEL | 048-647-2111 | ||||||
| sh2-mya@jichi.ac.jp | |||||||
| Public contact | |||||||
| Name of contact person |
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| Organization | Jichi Medical University, Saitama Medical Center | ||||||
| Division name | Department of Urology | ||||||
| Zip code | 3308503 | ||||||
| Address | 1-847, Amanuma-cho, Omiya-ku, Saitama City, Saitama, Japan | ||||||
| TEL | 048-647-2111 | ||||||
| Homepage URL | |||||||
| sh2-mya@jichi.ac.jp | |||||||
| Sponsor | |
| Institute | Jichi Medical University, Saitama Medical Center |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Jichi Medical University, Saitama Medical Center |
| Organization | |
| Division | |
| Category of Funding Organization | Other |
| Nationality of Funding Organization | |
| Other related organizations | |
| Co-sponsor | |
| Name of secondary funder(s) | |
| IRB Contact (For public release) | |
| Organization | Jichi Medical University Saitama Medical Center |
| Address | 1-847 Amanuma-cho Omiya-ku Saitama City Saitama Japan |
| Tel | 0486472111 |
| sh2-mya@jichi.ac.jp | |
| Secondary IDs | |
| Secondary IDs | NO |
| Study ID_1 | |
| Org. issuing International ID_1 | |
| Study ID_2 | |
| Org. issuing International ID_2 | |
| IND to MHLW | |
| Institutions | |
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| Date of disclosure of the study information |
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| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| Result | |
| URL related to results and publications | |
| Number of participants that the trial has enrolled | |
| Results | |
| Results date posted | |
| Results Delayed | |
| Results Delay Reason | |
| Date of the first journal publication of results | |
| Baseline Characteristics | |
| Participant flow | |
| Adverse events | |
| Outcome measures | |
| Plan to share IPD | |
| IPD sharing Plan description | |
| Progress | |||||||
| Recruitment status | Enrolling by invitation | ||||||
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| Other | |
| Other related information | |
| Management information | |||||||
| Registered date |
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| Last modified on |
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000032168 |