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NCT01804114 · ClinicalTrials.gov registry record · NA

Continuous Local Anesthetic Infusion Following Hernia Repair

A NA study, sponsored by Endeavor Health.

Completed
Registry status
NA
Development phase
31
Enrollment target

NCT01804114 is a NA study that has completed, run by Endeavor Health. The registered enrollment target is 31 participants.

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The verdict

NCT01804114, a NA study, has completed, sponsored by Endeavor Health.

COMPLETED
Registry status
NA
Development phase
31 participants
Enrollment target

Study Summary

The primary endpoint of this study will determine if subjects receiving a continuous infusion of local anesthetic following laparoscopic ventral hernia repair, with the pain pump installed as described to treat post surgical pain will have a lower incidence of pain than those patients treated with a placebo, saline-filled pain pump.The secondary endpoint of this study will determine if subjects receiving a continuous infusion of local anesthetic following laparoscopic ventral hernia repair, with the pain pump installed as described to treat post surgical pain will have a lower utilization of narcotic analgesic medication than those patients treated with the placebo, saline-filled pain pump.

Interventions

  • PROCEDURE Pain management following hernia repair
  • PROCEDURE Placebo for pain management following hernia repair

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2012-03
Est. Completion 2015-10
Phase NA

Sponsor

Endeavor Health

94 total trials

What the Registry Record Tells You About NCT01804114

The ClinicalTrials.gov registry entry for NCT01804114 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Endeavor Health, which has 94 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Pain management following hernia repair is the first listed.

NCT01804114 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01804114 about?

NCT01804114 is a clinical study titled "Continuous Local Anesthetic Infusion Following Hernia Repair". The primary endpoint of this study will determine if subjects receiving a continuous infusion of local anesthetic following laparoscopic ventral hernia repair, with the pain pump installed as described to treat post surgical pain will have a lower incidence of pain than those patients treated with a...

What is the current status of trial NCT01804114?

This trial is currently completed. It is a NA study. The enrollment target is 31 participants. The study started on 2012-03. Estimated completion is 2015-10.

What interventions are being tested in trial NCT01804114?

The interventions under investigation include: Pain management following hernia repair (PROCEDURE), Placebo for pain management following hernia repair (PROCEDURE).

Who is sponsoring clinical trial NCT01804114?

This trial is sponsored by Endeavor Health, which has 94 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.