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NCT04353687 · ClinicalTrials.gov registry record

Early Surgeon Experience With Robotic-Assisted Inguinal Hernia Repair

A clinical trial of Hernia, Inguinal, sponsored by Intuitive Surgical.

Active
Registry status
6
Enrollment target
1
Study location

NCT04353687 is a study of Hernia, Inguinal that is active but no longer recruiting, run by Intuitive Surgical. The registered enrollment target is 6 participants, below the 117-participant average among 4 other Hernia, Inguinal trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04353687, a study of Hernia, Inguinal, is active but no longer recruiting, sponsored by Intuitive Surgical.

ACTIVE NOT RECRUITING
Registry status
6 participants
Enrollment target
1
Study location

Study Summary

The primary objective of this study is to evaluate the progression of surgeon efficiency and proficiency of traditionally open or laparoscopic surgeons performing robotic-assisted inguinal hernia repair throughout their learning curve.

Conditions Studied

Interventions

  • DEVICE Robotic-assisted inguinal hernia repair

Study Locations (1)

Virginia

  • Riverside Hospital - Newport News

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2020-03-17
Est. Completion 2024-06-30

Sponsor

Intuitive Surgical

40 total trials

What the Registry Record Tells You About NCT04353687

The ClinicalTrials.gov registry entry for NCT04353687 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 6 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 117-participant average among 4 other Hernia, Inguinal trials with a reported enrollment target (95% lower). The listed sponsor is Intuitive Surgical, which has 40 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hernia, Inguinal appearing as the primary indexed condition, and to 1 intervention - of which Robotic-assisted inguinal hernia repair is the first listed.

NCT04353687 reports 1 study location spanning 1 distinct geographic area - top geographies include Virginia.

Frequently Asked Questions

What is clinical trial NCT04353687 about?

NCT04353687 is a clinical study titled "Early Surgeon Experience With Robotic-Assisted Inguinal Hernia Repair". The primary objective of this study is to evaluate the progression of surgeon efficiency and proficiency of traditionally open or laparoscopic surgeons performing robotic-assisted inguinal hernia repair throughout their learning curve.

What is the current status of trial NCT04353687?

This trial is currently active not recruiting. The enrollment target is 6 participants. The study started on 2020-03-17. Estimated completion is 2024-06-30.

What conditions does trial NCT04353687 study?

This clinical trial studies the following conditions: Hernia, Inguinal.

What interventions are being tested in trial NCT04353687?

The interventions under investigation include: Robotic-assisted inguinal hernia repair (DEVICE).

Who is sponsoring clinical trial NCT04353687?

This trial is sponsored by Intuitive Surgical, which has 40 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04353687 being conducted?

This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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