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NCT01982838 · ClinicalTrials.gov registry record · NA
Effects of Analgesic Techniques on Duration of Spontaneously Laboring Patients
A NA study, sponsored by Northwestern University.
- Terminated
- Registry status
- NA
- Development phase
- 129
- Enrollment target
NCT01982838 is a NA study that was terminated before completion, run by Northwestern University. The registered enrollment target is 129 participants.
The verdict
NCT01982838, a NA study, was terminated before completion, sponsored by Northwestern University.
- TERMINATED
- Registry status
- NA
- Development phase
- 129 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if there is a difference in the duration of the first stage of labor in nulliparous women in spontaneous labor with whom analgesia is maintained with a combined spinal epidural (CSE) technique versus nulliparous women in spontaneous labor with whom an epidural de novo technique is utilized. The investigators hypothesize that the duration of the first stage of labor will be no different in nulliparous patients who receive either intrathecal fentanyl or intrathecal fentanyl and bupivacaine, as part of a CSE technique. However, the duration of the first stage of labor will be shorter in parturients who receive intrathecal analgesia (as part of a CSE technique) compared to those who receive an epidural de novo technique with fentanyl and bupivacaine.
Interventions
- PROCEDURE CSE
- PROCEDURE Epidural de novo
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 129 participants |
| Start Date | 2010-07 |
| Est. Completion | 2014-03 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01982838
The ClinicalTrials.gov registry entry for NCT01982838 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 129 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 2 interventions - of which CSE is the first listed.
NCT01982838 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01982838 about?
NCT01982838 is a clinical study titled "Effects of Analgesic Techniques on Duration of Spontaneously Laboring Patients". The purpose of this study is to determine if there is a difference in the duration of the first stage of labor in nulliparous women in spontaneous labor with whom analgesia is maintained with a combined spinal epidural (CSE) technique versus nulliparous women in spontaneous labor with whom an epidur...
What is the current status of trial NCT01982838?
This trial is currently terminated. It is a NA study. The enrollment target is 129 participants. The study started on 2010-07. Estimated completion is 2014-03.
What interventions are being tested in trial NCT01982838?
The interventions under investigation include: CSE (PROCEDURE), Epidural de novo (PROCEDURE).
Who is sponsoring clinical trial NCT01982838?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
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