The Performance of da Vinci SP System on Extraperitoneal Approach Radical Prostatectomy

NCT ID: NCT05403190

Last Updated: 2023-02-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-08-01

Study Completion Date

2023-11-30

Brief Summary

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The objective of this study is to evaluate the performance and safety of da Vinci Single Port (SP) system on the surgery for extraperitoneal approach radical prostatectomy

Detailed Description

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Enrolled subjects would receive extraperitoneal approach radical prostatectomy using da Vinci SP system and be assessed at baseline (preoperatively), during hospitalization, and postoperatively (at 1 month +/-4 days, 3 month +/- 7 days, 6 months +/- 10 days, 12month +/-14 days). The preoperative assessment includes any diagnostic tests to confirm the subjects' cancer status and eligibility for the intervention under consideration such as transrectal or transperineal biopsy, image studies for staging including MRI/CT and bone scan, and cardiopulmonary tests to evaluate risks for anesthesia. The hospitalization assessment includes the collection of perioperative and postoperative details, conversions, and complications. The postoperative assessment includes regular follow up studies to evaluate cancer status and functional outcome (For sexual function, the International Index of Erectile Function (IIEF-5) would be recorded before and after the surgery. For continence, the number of pads per day and 24hr total weight of pads would be recorded. No pad used or one safe pad per day with net wet ≤ 50gm would be considered as continent. International Prostate Symptom Score (IPSS) wound be recorded before and after the surgery to access voiding function).

Conditions

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Prostate Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Study arm

Patients with prostate cancer

Group Type EXPERIMENTAL

da Vinci SP system

Intervention Type DEVICE

using da Vinci SP system to perform extraperitoneal approach radical prostatectomy

Interventions

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da Vinci SP system

using da Vinci SP system to perform extraperitoneal approach radical prostatectomy

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Patients with biopsy-proved prostate cancer
2. Stage clinical T1-T2N0M0
3. Prostate volume ≦ 70cm (by transrectal ultrasound or other image studies)
4. BMI ≦ 35 kg/m
5. Low priority of nerve sparing (pre-op sexual dysfunction or don't care about sexual function)
6. Age between 18 and 78 years old
7. Suitable for minimally invasive surgery
8. Patients willing and able to provide informed consent
9. Patients willing and able to comply with study protocol requirements and follow-up

Exclusion Criteria

1. Previous abdominal or pelvic major operation history
2. Previous radiation treatment to the pelvic area
3. Patients received transurethral resection of prostate in three months
4. Severe concomitant illness that drastically shortens life expectancy or increases risk of therapeutic interventions

* Severe heart disease (NYHA functional class III-IV)
* Severe lung disease (GOLD Group C-D)
5. Anatomy unsuitable for endoscopic visualization or minimally invasive surgery
6. Hemodynamic or respiratory instability after anesthesia
7. Working space restriction (e.g. kyphosis or severe scoliosis)
8. Emergency surgery
9. Untreated active infection
10. vulnerable populations
Minimum Eligible Age

18 Years

Maximum Eligible Age

78 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Intuitive Surgical

INDUSTRY

Sponsor Role collaborator

Chang Gung Memorial Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Chun-Te Wu, Professor, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Chang Gung Memorial Hospital at Keelung

Locations

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Chang Gung Memorial Hospital

Taoyuan, , Taiwan

Site Status RECRUITING

Countries

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Taiwan

Central Contacts

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Po-Hung Lin, MD

Role: CONTACT

+886975366240

Hung-Jen Wang, MD

Role: CONTACT

+886975356239

Facility Contacts

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Po-Hung Lin

Role: primary

+886975366240

Other Identifiers

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202101419A0C601

Identifier Type: -

Identifier Source: org_study_id

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