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NCT00443560 · ClinicalTrials.gov registry record
The Association Between Decreasing Labor Analgesia Epidural Infusion and Forceps Delivery
A clinical trial, sponsored by Northwestern University.
- Completed
- Registry status
- 2,162
- Enrollment target
NCT00443560 is a clinical trial that has completed, run by Northwestern University. The registered enrollment target is 2,162 participants.
The verdict
NCT00443560 has completed, sponsored by Northwestern University.
- COMPLETED
- Registry status
- 2,162 participants
- Enrollment target
Study Summary
The objective of this study will be to compare epidural infusion management, specifically looking at infusion rate changes, in patients who receive forceps deliveries versus normal spontaneous vaginal deliveries. We will match patients based on time and date of delivery, as well as parity, in order to eliminate these variables as potential con-founders. We hypothesize patients who require a decrease in their basal labor analgesia epidural infusion rate will have an increased incidence of forceps delivery.
Interventions
- OTHER Case controlled analysis of epidural labor analgesia patterns
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,162 participants |
| Start Date | 2006-01 |
| Est. Completion | 2006-03 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00443560
The ClinicalTrials.gov registry entry for NCT00443560 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 2,162 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 1 intervention - of which Case controlled analysis of epidural labor analgesia patterns is the first listed.
NCT00443560 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00443560 about?
NCT00443560 is a clinical study titled "The Association Between Decreasing Labor Analgesia Epidural Infusion and Forceps Delivery". The objective of this study will be to compare epidural infusion management, specifically looking at infusion rate changes, in patients who receive forceps deliveries versus normal spontaneous vaginal deliveries. We will match patients based on time and date of delivery, as well as parity, in order ...
What is the current status of trial NCT00443560?
This trial is currently completed. The enrollment target is 2,162 participants. The study started on 2006-01. Estimated completion is 2006-03.
What interventions are being tested in trial NCT00443560?
The interventions under investigation include: Case controlled analysis of epidural labor analgesia patterns (OTHER).
Who is sponsoring clinical trial NCT00443560?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
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