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

NCT00938964 · ClinicalTrials.gov registry record · NA

Lidocaine For Neuroprotection During Cardiac Surgery

A NA study, sponsored by Duke University.

Completed
Registry status
NA
Development phase
550
Enrollment target

NCT00938964: Completed NA study, sponsored by Duke University.

NCT00938964 is a NA study that has completed, run by Duke University. The registered enrollment target is 550 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00938964, a NA study, has completed, sponsored by Duke University.

COMPLETED
Registry status
NA
Development phase
550 participants
Enrollment target

Study Summary

The purpose of this study is to see if a drug called lidocaine prevents cognitive injury (a decline in mental abilities) after heart surgery. Lidocaine is currently FDA approved and is commonly used for treating some heart rhythm disorders and for regional anesthesia (blocking nerves). The investigators are enrolling subjects in this research project to see if lidocaine will reduce the high incidence of cognitive injury seen after heart surgery. As part of this study, the investigators will also evaluate the relationship between cognitive injury and genetic makeup and the chemical changes in the subjects blood during and after surgery.

Primary Outcome

To characterize cognitive function over time, while minimizing potential redundancy in the cognitive measures, a factor analysis was performed on the 14 cognitive test scores from baseline. We chose a five-factor solution, which represents 5 cognitive domains: structured verbal memory, unstructured verbal memory, executive function, visual memory and attention/concentration. To quantify overall cognitive function, a baseline cognitive index was first calculated as the mean of the 5 preoperative

Interventions

  • DRUG Placebo
  • DRUG Lidocaine

Trial Details

FieldValue
Enrollment Target 550 participants
Start Date 2009-07
Est. Completion 2017-05-23
Phase NA
Duke University

1,725 total trials

What the finished NCT00938964 record still lists

NCT00938964 is an interventional study that assigns participants to a tested intervention. The registered 550 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (61% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00938964 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00938964 about?

NCT00938964 is a clinical study titled "Lidocaine For Neuroprotection During Cardiac Surgery". The purpose of this study is to see if a drug called lidocaine prevents cognitive injury (a decline in mental abilities) after heart surgery. Lidocaine is currently FDA approved and is commonly used for treating some heart rhythm disorders and for regional anesthesia (blocking nerves). The investiga...

What is the current status of trial NCT00938964?

This trial is currently completed. It is a NA study. The enrollment target is 550 participants. The study started on 2009-07. Estimated completion is 2017-05-23.

What interventions are being tested in trial NCT00938964?

The interventions under investigation include: Placebo (DRUG), Lidocaine (DRUG).

Who is sponsoring clinical trial NCT00938964?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00938964's enrollment target sits among peer trials

550 184th of 2000 higher than 1,815 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

  • NCT01852448 · 550 participants

    Genetics of Insulin and Incretins in Cystic Fibrosis

  • NCT02995252 · 550 participants

    The HOPE Study: Characterizing Patients With Hepatitis B and C

  • NCT03474913 · 550 participants

    Upright MRI for Prostate Cancer Screening

  • NCT04761120 · 550 participants

    Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study

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 NCT00938964, the US trial registry maintained by the National Library of Medicine. NCT00938964 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.