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CompletedNCT04982822Updated Jun 25, 2024

Novel Senhance Robotic System in Urologic Surgery: Its Clinical Application and Implication

An observational study in Urologic Diseases and Surgery, sponsored by National Taiwan University Hospital. Completed at 1 site in Taiwan. Open to participants aged 18 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-25.

Sponsored by National Taiwan University Hospital · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
314
Ages
18 Years to 90 Years
Sex
All
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Study summary

An observational study to collect data from the participants who received urologic surgeries using the Senhance Robotic system.

Read the detailed description

This is an observational study and investigators will collect peri-operative demographic data, and short-term outcomes (3-6 months) from the participants who received minimal invasive surgeries using Senhance robotic system in the National Taiwan University Hospital Yunlin Branch, Urology Department. The investigators want to demonstrate if the robotic system is safe and feasible in urologic laparoscopic surgeries.

The operation included TEP, radical prostatectomy, radical nephrectomy (nephroureterectomy) , adrenalectomy, radical cystectomy, and ureter surgery et al.

up to 2022/12, we had recruited 127 TEP, 83 radical prostatectomies, 17 adrenalectomies, 40 nephrectomies, 29 partial nephrectomies, 13 radical cystectomies and 18 other surgeries, such as ureter surgery

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Conditions studied

  • Urologic Diseases
  • Surgery

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Keywords

  • Urology
  • Senhance
  • Robotic surgical system
  • Laparoscopic surgery
03

In context

Urologic Diseases

193 studies on the registry are indexed under Urologic Diseases; 51 are open to participants now.

This study's enrollment of 314 is above the median of 200 across 49 observational studies indexed under Urologic Diseases.

Browse Urologic Diseases studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,563 studies on the registry; 569 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study populations consisted of aged from 18 years old to 90 years old and had will to receive laparoscopic surgeries using the Senhance robotic system.

The were excluded if there's major severe cardio-pulmonary condition or had received extensive abdominal surgeries.

Eligibility criteria

Patients undergo laparoscopic urologic surgeries

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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
314 participants (actual)
06

What researchers measure

Primary outcomes

  1. Peri-operative complications

    Using Clavien-Dindo classification to record the safety outcome

    Time frame: postoperative 30 days

  2. short-term outcome

    the short-term outcome was according to a different surgery, such as post-operative 3 months PSA, incontinence rate in radical prostatectomy,

    Time frame: 3-6 months

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Study locations

1 site
  • National Taiwan University Hospital
    Taipei, Outside U.S./Canada, Taiwan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 25, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04982822
Lead sponsor
National Taiwan University Hospital
Responsible party
Sponsor
First posted
Jul 29, 2021
Start date
Dec 1, 2020
Primary completion
Dec 31, 2022
Completion
Jan 31, 2024
Last update
Jun 25, 2024

Study contacts

LunHsiang Yuan, MD
principal investigator · National Taiwan University Hospital Yunlin Branch

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

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