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NCT00846651 · ClinicalTrials.gov registry record · Phase 4
Spinal Anesthesia Induced Hypotension During Cesarean Section
A Phase 4 study, sponsored by Milton S. Hershey Medical Center.
- Completed
- Registry status
- Phase 4
- Development phase
- 82
- Enrollment target
NCT00846651 is a Phase 4 study that has completed, run by Milton S. Hershey Medical Center. The registered enrollment target is 82 participants.
The verdict
NCT00846651, a Phase 4 study, has completed, sponsored by Milton S. Hershey Medical Center.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 82 participants
- Enrollment target
Study Summary
The purpose of this study is to compare two methods for preventing low blood pressure associated with spinal anesthesia during Cesarean sections.
Interventions
- DRUG phenylephrine infusion
- OTHER Colloid administration
- OTHER Crystalloid administration
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 82 participants |
| Start Date | 2009-02 |
| Est. Completion | 2010-02 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00846651
The ClinicalTrials.gov registry entry for NCT00846651 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 82 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Milton S. Hershey Medical Center, which has 396 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which phenylephrine infusion is the first listed.
NCT00846651 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00846651 about?
NCT00846651 is a clinical study titled "Spinal Anesthesia Induced Hypotension During Cesarean Section". The purpose of this study is to compare two methods for preventing low blood pressure associated with spinal anesthesia during Cesarean sections.
What is the current status of trial NCT00846651?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 82 participants. The study started on 2009-02. Estimated completion is 2010-02.
What interventions are being tested in trial NCT00846651?
The interventions under investigation include: phenylephrine infusion (DRUG), Colloid administration (OTHER), Crystalloid administration (OTHER).
Who is sponsoring clinical trial NCT00846651?
This trial is sponsored by Milton S. Hershey Medical Center, which has 396 total clinical trials registered on ClinicalTrials.gov.
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