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NCT00787176 · ClinicalTrials.gov registry record · NA
The Association Between Fluid Administration, Oxytocin Administration, and Fetal Heart Rate Changes
A NA study, sponsored by Northwestern University.
- Terminated
- Registry status
- NA
- Development phase
- 251
- Enrollment target
NCT00787176 is a NA study that was terminated before completion, run by Northwestern University. The registered enrollment target is 251 participants.
The verdict
NCT00787176, a NA study, was terminated before completion, sponsored by Northwestern University.
- TERMINATED
- Registry status
- NA
- Development phase
- 251 participants
- Enrollment target
Study Summary
Fetal heart rate patterns are an important parameter in the diagnosis of non-reassuring fetal status. Combined-spinal epidural analgesia is a method of initiating labor analgesia used by approximately 90% of the parturients at Prentice Women's Hospital. Optimizing the variables which could affect fetal heart rate patterns at the time of initiation of analgesia, such as fluid administration and oxytocin management, could help us provide better care for our patients and their fetuses. Hypotheses: The combination of fluid administration and lower doses of oxytocin administration will have fewer adverse fetal heart rate changes in the first 60 minutes following initiation of labor analgesia.
Interventions
- DRUG Group A Intravenous bolus of 1000 ml lactated ringers solution
- DRUG Group B Intravenous bolus bolus 1000 ml lactated ringers solution oxytocin decrease to 1/2 current rate
- DRUG Group C 125 mL/hr of lactated ringers
- DRUG Group D 125 mL/hr lactated ringers oxytocin decreased to 1/2 current rate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 251 participants |
| Start Date | 2007-09 |
| Est. Completion | 2012-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00787176
The ClinicalTrials.gov registry entry for NCT00787176 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 251 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwestern University, which has 1,209 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 4 interventions - of which Group A Intravenous bolus of 1000 ml lactated ringers solution is the first listed.
NCT00787176 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00787176 about?
NCT00787176 is a clinical study titled "The Association Between Fluid Administration, Oxytocin Administration, and Fetal Heart Rate Changes". Fetal heart rate patterns are an important parameter in the diagnosis of non-reassuring fetal status. Combined-spinal epidural analgesia is a method of initiating labor analgesia used by approximately 90% of the parturients at Prentice Women's Hospital. Optimizing the variables which could affect fe...
What is the current status of trial NCT00787176?
This trial is currently terminated. It is a NA study. The enrollment target is 251 participants. The study started on 2007-09. Estimated completion is 2012-07.
What interventions are being tested in trial NCT00787176?
The interventions under investigation include: Group A Intravenous bolus of 1000 ml lactated ringers solution (DRUG), Group B Intravenous bolus bolus 1000 ml lactated ringers solution oxytocin decrease to 1/2 current rate (DRUG), Group C 125 mL/hr of lactated ringers (DRUG), Group D 125 mL/hr lactated ringers oxytocin decreased to 1/2 current rate (DRUG).
Who is sponsoring clinical trial NCT00787176?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
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