CClinicalTrials.gg
CompletedNCT00225043Updated Jun 2, 2008

A Randomized, Double-Blind, Trial Comparing Epinephrine Versus Phenylephrine as a Vasoconstrictor in Regional Anesthesia for Upper Extremity Surgery

An interventional study of Epinephrine/phenylephrine in Healthy, sponsored by New York Presbyterian Brooklyn Methodist Hospital. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2008-06-02.

Sponsored by New York Presbyterian Brooklyn Methodist Hospital · Not applicable and Interventional

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The study involves research, the purpose of which is to compare three different drug mixtures (Epinephrine, Phenylephrine 25 µg, or Phenylephrine 50 µg). Specifically, how long each medicine lasts will be studied.

02

Conditions studied

  • Healthy
03

In context

Lead sponsor

New York Presbyterian Brooklyn Methodist Hospital is the lead sponsor of 15 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Shoulder surgery with regional anesthesia

Exclusion criteria

Exclusion Criteria:

  • Shoulder surgery with general anesthesia unhealthy
05

Study design

Phase
Not applicable
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double
Enrollment
60 participants (actual)

Interventions

  • DrugEpinephrine/phenylephrine
06

Study locations

1 site
  • New York Methodist Hospital
    Brooklyn, New York 11215, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 2, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00225043
Lead sponsor
New York Presbyterian Brooklyn Methodist Hospital
First posted
Sep 23, 2005
Start date
Jun 2005
Primary completion
Aug 2007
Completion
Aug 2007
Last update
Jun 2, 2008

Study contacts

Joel Yarmush, MD, MPA
principal investigator · New York Presbyterian Brooklyn Methodist Hospital
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2008. You cannot join it, but the record below documents what was studied.

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