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NCT04074200 · ClinicalTrials.gov registry record

Pain and Quality of Life After Inguinal Hernia Repair

A clinical trial, sponsored by Intuitive Surgical.

Completed
Registry status
156
Enrollment target

NCT04074200: Completed study, sponsored by Intuitive Surgical.

NCT04074200 is a clinical trial that has completed, run by Intuitive Surgical. The registered enrollment target is 156 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04074200 has completed, sponsored by Intuitive Surgical.

COMPLETED
Registry status
156 participants
Enrollment target

Study Summary

This study aims to explore the difference in outcomes relating to pain and quality of life after open, laparoscopic, and robotic-assisted inguinal hernia repair.

Primary Outcome

Change in patient-reported pain scores assessed by the Brief Pain Inventory Tool (BPI), with scores on individual questions ranging from 0% (no relief) to 100% (complete relief) or 0 (no pain/does not interfere) to 10 (pain as bad as you can imagine/completely interferes).

Interventions

  • PROCEDURE Laparoscopic Inguinal Hernia Repair
  • PROCEDURE Open Inguinal Hernia Repair
  • DEVICE Robotic-Assisted Inguinal Hernia Repair

Trial Details

FieldValue
Enrollment Target 156 participants
Start Date 2019-08-26
Est. Completion 2023-07-06
Intuitive Surgical

40 total trials

What the finished NCT04074200 record still lists

NCT04074200 is an observational study that tracks outcomes without assigning an intervention. The registered 156 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 3 interventions - of which Laparoscopic Inguinal Hernia Repair is the first listed.

NCT04074200 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04074200 about?

NCT04074200 is a clinical study titled "Pain and Quality of Life After Inguinal Hernia Repair". This study aims to explore the difference in outcomes relating to pain and quality of life after open, laparoscopic, and robotic-assisted inguinal hernia repair.

What is the current status of trial NCT04074200?

This trial is currently completed. The enrollment target is 156 participants. The study started on 2019-08-26. Estimated completion is 2023-07-06.

What interventions are being tested in trial NCT04074200?

The interventions under investigation include: Laparoscopic Inguinal Hernia Repair (PROCEDURE), Open Inguinal Hernia Repair (PROCEDURE), Robotic-Assisted Inguinal Hernia Repair (DEVICE).

Who is sponsoring clinical trial NCT04074200?

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

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Source: ClinicalTrials.gov NCT04074200, the US trial registry maintained by the National Library of Medicine. NCT04074200 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.