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NCT00779467 · ClinicalTrials.gov registry record · Phase 1

Epidural Neostigmine for Labor Pain

A Phase 1 study of Labor Pain, sponsored by Wake Forest University.

Completed
Registry status
Phase 1
Development phase
200
Enrollment target
1
Study location

NCT00779467: Completed Phase 1 study of Labor Pain, sponsored by Wake Forest University.

NCT00779467 is a Phase 1 study of Labor Pain that has completed, run by Wake Forest University. The registered enrollment target is 200 participants, roughly in line with the 190-participant average among 14 other Labor Pain trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00779467, a Phase 1 study of Labor Pain, has completed, sponsored by Wake Forest University.

COMPLETED
Registry status
Phase 1
Development phase
200 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to see which dose of epidural neostigmine is the best additive to use with the numbing medication used in an epidural during labor.

Primary Outcome

Median hourly total bupivacaine consumption. Drug amount consumed per hour of each group (arm)

Conditions Studied

Interventions

  • DRUG Bupivacaine
  • DRUG Neostigmine
  • DRUG fentanyl

Study Locations (1)

North Carolina

  • Forsyth Medical Center - Winston-Salem

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2008-10
Est. Completion 2013-11
Phase Phase 1
Wake Forest University

100 total trials

What the finished NCT00779467 record still lists

NCT00779467 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 190-participant average among 14 other Labor Pain trials with a reported enrollment target.

The record links to 1 condition, with Labor Pain appearing as the primary indexed condition, and to 3 interventions - of which Bupivacaine is the first listed.

NCT00779467 reports a single indexed study location in North Carolina.

Frequently Asked Questions

What is clinical trial NCT00779467 about?

NCT00779467 is a clinical study titled "Epidural Neostigmine for Labor Pain". The purpose of this study is to see which dose of epidural neostigmine is the best additive to use with the numbing medication used in an epidural during labor.

What is the current status of trial NCT00779467?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 200 participants. The study started on 2008-10. Estimated completion is 2013-11.

What conditions does trial NCT00779467 study?

This clinical trial studies the following conditions: Labor Pain.

What interventions are being tested in trial NCT00779467?

The interventions under investigation include: Bupivacaine (DRUG), Neostigmine (DRUG), fentanyl (DRUG).

Who is sponsoring clinical trial NCT00779467?

This trial is sponsored by Wake Forest University, which has 100 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00779467 being conducted?

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

Similar trials for Labor Pain

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00779467's enrollment target sits among peer trials

200 4th of 14 higher than 11 of 14 other Labor Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Labor Pain 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 NCT00779467, the US trial registry maintained by the National Library of Medicine. NCT00779467 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.