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NCT00583011 · ClinicalTrials.gov registry record · NA

Local Anesthesia and Pain Perception During an Amniocentesis

A NA study of Pregnancy, sponsored by University of Oklahoma.

Completed
Registry status
NA
Development phase
76
Enrollment target
1
Study location

NCT00583011 is a NA study of Pregnancy that has completed, run by University of Oklahoma. The registered enrollment target is 76 participants, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00583011, a NA study of Pregnancy, has completed, sponsored by University of Oklahoma.

COMPLETED
Registry status
NA
Development phase
76 participants
Enrollment target
1
Study location

Study Summary

This study is been designed to answer the question of whether local anesthesia (1% lidocaine) decreases the perception of pain associated with amniocentesis in a randomized double blind placebo controlled manner. Our objective is to determine the effect of local anesthesia on the maternal pain perception from an amniocentesis.

Conditions Studied

Interventions

  • DRUG Local Anesthesia
  • DRUG Placebo Group

Study Locations (1)

Oklahoma

  • University of Oklahoma Health Sciences Center - Oklahoma City

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2007-10
Est. Completion 2011-05
Phase NA

Sponsor

University of Oklahoma

358 total trials

What the Registry Record Tells You About NCT00583011

The ClinicalTrials.gov registry entry for NCT00583011 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 76 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (91% lower). The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pregnancy appearing as the primary indexed condition, and to 2 interventions - of which Local Anesthesia is the first listed.

NCT00583011 reports 1 study location spanning 1 distinct geographic area - top geographies include Oklahoma.

Frequently Asked Questions

What is clinical trial NCT00583011 about?

NCT00583011 is a clinical study titled "Local Anesthesia and Pain Perception During an Amniocentesis". This study is been designed to answer the question of whether local anesthesia (1% lidocaine) decreases the perception of pain associated with amniocentesis in a randomized double blind placebo controlled manner. Our objective is to determine the effect of local anesthesia on the maternal pain perce...

What is the current status of trial NCT00583011?

This trial is currently completed. It is a NA study. The enrollment target is 76 participants. The study started on 2007-10. Estimated completion is 2011-05.

What conditions does trial NCT00583011 study?

This clinical trial studies the following conditions: Pregnancy.

What interventions are being tested in trial NCT00583011?

The interventions under investigation include: Local Anesthesia (DRUG), Placebo Group (DRUG).

Who is sponsoring clinical trial NCT00583011?

This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00583011 being conducted?

This trial has 1 study location across Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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