Prevention of Lymphoceles After Robotic PLND

NCT ID: NCT02035475

Last Updated: 2016-11-15

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-08-31

Study Completion Date

2014-12-31

Brief Summary

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The EndoWrist One Vessel Sealer is a bipolar electrosurgical instrument for use with the da Vinci Si robotic surgical system. It is intended for bipolar coagulation and mechanical transection of vessels up to 7 mm in diameter and tissue bundles that fit within the jaws of the instrument. Their use in this study will be to perform tissue transection during PLND such that the intended use is within the FDA-approved domain for this instrument. Investigators intend to identify whether its use for PLND reduces lymphoceles given that the device is known to seal vessels up to 7 mm, which is much larger than lymphatic vessels encountered during PLND. Because the instrument is new and has been FDA approved for less than one year, there is no published literature regarding its use to date.

Our hypothesis is that using the Vessel Sealer on a single side of the pelvis will reduce the incidence of screening detected lymphoceles on that side. Investigators propose a total sample size of 120 patients.

Detailed Description

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Investigators propose a prospective, randomized, single-blinded study of patients diagnosed with pelvic cancer who are electing to undergo robotic surgery with PLND. The patients in our trial will be pelvic cancer patients at risk for lymphocele after PLND. Given the safe nature of the product and the patient's risk for lymphocele after PLND and subsequent potential morbidity, there is justification to give patients the option for inclusion in the study. Investigators intend to determine whether the rate of lymphocele formation after PLND at the time of robotic pelvic cancer surgery can be reduced by using the robotic Vessel Sealer unilaterally for the lymph node dissection. The side of the pelvis of each patient will be randomly selected by Excel's® random number function "RAND()" to receive the Vessel Sealer dissection. Investigators intend to use this device unilaterally so the contralateral side can serve as an internal control and eliminate patient specific confounding variables such as BMI, and surgeon specific factors such as degree and method of hemostasis utilized by each surgeon. In addition, Dr. Abaza will be the only surgeon performing these procedures, eliminating variation in technique between surgeons.

Conditions

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Lymphoceles Prostate Cancer

Keywords

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Prevention Pelvic Lymph Node Dissection Lymphoceles Prostate Malignancies daVinci Vessel Sealer EndoWrist One

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Intuitive Vessel Sealer

Investigators intend to use this device unilaterally so the contralateral side can serve as an internal control.

Group Type ACTIVE_COMPARATOR

Intuitive Vessel Sealer

Intervention Type DEVICE

Investigators intend to use this device unilaterally so the contralateral side can serve as an internal control.

Maryland Bipolar Cautery

Investigators intend to use this device unilaterally so the contralateral side can serve as an internal control.

Group Type ACTIVE_COMPARATOR

Intuitive Vessel Sealer

Intervention Type DEVICE

Investigators intend to use this device unilaterally so the contralateral side can serve as an internal control.

Interventions

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Intuitive Vessel Sealer

Investigators intend to use this device unilaterally so the contralateral side can serve as an internal control.

Intervention Type DEVICE

Other Intervention Names

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EndoWrist One Vessel Sealer

Eligibility Criteria

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Inclusion Criteria

* Age 18 or older
* Candidate scheduled to undergo robotic prostatectomy surgery with PLND

Exclusion Criteria

* Age \< 18
* Unable to give informed consent
* Non-English speaking
* Not a candidate for robotic surgery for any reason
Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Intuitive Surgical

INDUSTRY

Sponsor Role collaborator

OhioHealth

OTHER

Sponsor Role lead

Responsible Party

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Ronney Abaza

Medical Director Robotic Surgery

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ronney Abaza, MD, FACS

Role: PRINCIPAL_INVESTIGATOR

OhioHealth

Locations

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Dublin Methodist Hospital

Columbus, Ohio, United States

Site Status

Countries

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United States

References

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Abaza R, Henderson SJ, Martinez O. Robotic Vessel Sealer Device for Lymphocele Prevention After Pelvic Lymphadenectomy: Results of a Randomized Trial. J Laparoendosc Adv Surg Tech A. 2022 Jul;32(7):721-726. doi: 10.1089/lap.2021.0531. Epub 2021 Oct 22.

Reference Type DERIVED
PMID: 34677080 (View on PubMed)

Other Identifiers

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OH1-13-00471

Identifier Type: -

Identifier Source: org_study_id