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NCT00432991 · ClinicalTrials.gov registry record · Phase 2

Study of the Effect of Intramuscular Ephedrine on the Incidence of Nausea and Vomiting During Elective Cesarean Section

A Phase 2 study, sponsored by Weill Medical College of Cornell University.

Completed
Registry status
Phase 2
Development phase
53
Enrollment target

NCT00432991: Completed Phase 2 study, sponsored by Weill Medical College of Cornell University.

NCT00432991 is a Phase 2 study that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 53 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00432991, a Phase 2 study, has completed, sponsored by Weill Medical College of Cornell University.

COMPLETED
Registry status
Phase 2
Development phase
53 participants
Enrollment target

Study Summary

The purpose of this research study is to investigate if the incidence of nausea and vomiting that subjects experience during and after a Cesarean section can be reduced by giving a shot of the drug ephedrine into the thigh muscle at the time of spinal anesthesia administration.

Primary Outcome

Subject's self-rated nausea level on a scale of 0-3 immediately prior to induction of spinal anesthesia, where 0=no nausea, 1=mild nausea, 2=moderate nausea, and 3=severe nausea

Interventions

  • DRUG Saline Placebo
  • DRUG Ephedrine [Synonyms: Ephedra, Ephedrinum]

Trial Details

FieldValue
Enrollment Target 53 participants
Start Date 2007-02
Est. Completion 2010-09
Phase Phase 2

What the finished NCT00432991 record still lists

NCT00432991 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 53 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (60% lower).

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

NCT00432991 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00432991 about?

NCT00432991 is a clinical study titled "Study of the Effect of Intramuscular Ephedrine on the Incidence of Nausea and Vomiting During Elective Cesarean Section". The purpose of this research study is to investigate if the incidence of nausea and vomiting that subjects experience during and after a Cesarean section can be reduced by giving a shot of the drug ephedrine into the thigh muscle at the time of spinal anesthesia administration.

What is the current status of trial NCT00432991?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 53 participants. The study started on 2007-02. Estimated completion is 2010-09.

What interventions are being tested in trial NCT00432991?

The interventions under investigation include: Saline Placebo (DRUG), Ephedrine [Synonyms: Ephedra, Ephedrinum] (DRUG).

Who is sponsoring clinical trial NCT00432991?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00432991's enrollment target sits among peer trials

53 1171st of 2000 higher than 820 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00432991, the US trial registry maintained by the National Library of Medicine. NCT00432991 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.