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NCT02055053 · ClinicalTrials.gov registry record · Phase 4

Effects of Local Anesthesia on Post-operative Pain During Laparoscopic Inguinal Hernia Repair

A Phase 4 study, sponsored by Lahey Clinic.

Completed
Registry status
Phase 4
Development phase
70
Enrollment target

NCT02055053: Completed Phase 4 study, sponsored by Lahey Clinic.

NCT02055053 is a Phase 4 study that has completed, run by Lahey Clinic. The registered enrollment target is 70 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02055053, a Phase 4 study, has completed, sponsored by Lahey Clinic.

COMPLETED
Registry status
Phase 4
Development phase
70 participants
Enrollment target

Study Summary

To assess effect of local anesthetic into the preperitoneal space during laparoscopic hernia repair on post-operative pain.

Primary Outcome

Pain level at 4 hours after surgery VAS scale measures pain in whole numbers from 0 (no pain) to 10 (worst imaginable pain)

Interventions

  • DRUG 0.5% Bupivicaine

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2013-08
Est. Completion 2019-10-16
Phase Phase 4
Lahey Clinic

43 total trials

What the finished NCT02055053 record still lists

NCT02055053 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower).

The record links to 0 conditions, and to 1 intervention - of which 0.5% Bupivicaine is the first listed.

NCT02055053 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02055053 about?

NCT02055053 is a clinical study titled "Effects of Local Anesthesia on Post-operative Pain During Laparoscopic Inguinal Hernia Repair". To assess effect of local anesthetic into the preperitoneal space during laparoscopic hernia repair on post-operative pain.

What is the current status of trial NCT02055053?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 70 participants. The study started on 2013-08. Estimated completion is 2019-10-16.

What interventions are being tested in trial NCT02055053?

The interventions under investigation include: 0.5% Bupivicaine (DRUG).

Who is sponsoring clinical trial NCT02055053?

This trial is sponsored by Lahey Clinic, which has 43 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02055053's enrollment target sits among peer trials

70 1043rd of 2000 higher than 931 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02055053, the US trial registry maintained by the National Library of Medicine. NCT02055053 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.