Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00659633 · ClinicalTrials.gov registry record · NA

The Effect of Intravenous Lidocaine on Allodynia

A NA study, sponsored by University of Alabama at Birmingham.

Completed
Registry status
NA
Development phase
10
Enrollment target

NCT00659633: Completed NA study, sponsored by University of Alabama at Birmingham.

NCT00659633 is a NA study that has completed, run by University of Alabama at Birmingham. The registered enrollment target is 10 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00659633, a NA study, has completed, sponsored by University of Alabama at Birmingham.

COMPLETED
Registry status
NA
Development phase
10 participants
Enrollment target

Study Summary

The purpose of this study is to study if lidocaine, given intravenously, reduces pain.

Primary Outcome

Assessing heat pain perception (pain intensity) before, during, and after lidocaine infusion by means of patient self-report using a mechanical slide algometer. The mechanical slide algometer \[Price et al. (1994)\] looks like a ruler that exposes a red bar with the end-points: no pain (left) and most pain imaginable (right). The use the slider to express their perceived pain. On the back of the ruler a numerical scale ranging from 0 (no pain) to 10 (worst imaginable pain) translates the patien

Interventions

  • DRUG lidocaine

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2008-12
Est. Completion 2016-08
Phase NA
University of Alabama at Birmingham

1,160 total trials

What the finished NCT00659633 record still lists

NCT00659633 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

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

NCT00659633 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00659633 about?

NCT00659633 is a clinical study titled "The Effect of Intravenous Lidocaine on Allodynia". The purpose of this study is to study if lidocaine, given intravenously, reduces pain.

What is the current status of trial NCT00659633?

This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2008-12. Estimated completion is 2016-08.

What interventions are being tested in trial NCT00659633?

The interventions under investigation include: lidocaine (DRUG).

Who is sponsoring clinical trial NCT00659633?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00659633's enrollment target sits among peer trials

10 1927th of 2000 higher than 26 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00623389 · 10 participants · NA

    Evaluation of an Advanced Lower Extremity Neuroprostheses

  • NCT01241864 · 10 participants · Phase 2

    Islet Transplantation in Type 1 Diabetic Kidney Allograft

  • NCT01293214 · 10 participants · NA

    Vascularized Composite Allotransplantation for Multiple Extremity Amputations

  • NCT01474148 · 10 participants · NA

    A Neuroprosthesis for Seated Posture and Balance

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00659633, the US trial registry maintained by the National Library of Medicine. NCT00659633 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.