Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01861821 · ClinicalTrials.gov registry record · NA
Analgesic Efficacy of a Multiport Versus Uniport Flexible Catheter for Labor Epidural Analgesia
A NA study, sponsored by Baylor Research Institute.
- Completed
- Registry status
- NA
- Development phase
- 650
- Enrollment target
NCT01861821: Completed NA study, sponsored by Baylor Research Institute.
NCT01861821 is a NA study that has completed, run by Baylor Research Institute. The registered enrollment target is 650 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (54% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01861821, a NA study, has completed, sponsored by Baylor Research Institute.
- COMPLETED
- Registry status
- NA
- Development phase
- 650 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether multiple ports improve the analgesic efficacy of flexible catheters used for the provision of epidural analgesia during the entire continuum of labor and delivery
Primary Outcome
Complete analgesia is defined as the complete relief of pain during contractions following the administration of the above epidural medication without requiring further epidural medication/intervention.
Interventions
- DEVICE Multiport flexible catheter
- DEVICE Uniport flexible catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 650 participants |
| Start Date | 2011-11 |
| Est. Completion | 2013-06 |
| Phase | NA |
What the finished NCT01861821 record still lists
NCT01861821 is an interventional study that assigns participants to a tested intervention. The registered 650 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (54% lower).
The record links to 0 conditions, and to 2 interventions - of which Multiport flexible catheter is the first listed.
NCT01861821 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01861821 about?
NCT01861821 is a clinical study titled "Analgesic Efficacy of a Multiport Versus Uniport Flexible Catheter for Labor Epidural Analgesia". The purpose of this study is to determine whether multiple ports improve the analgesic efficacy of flexible catheters used for the provision of epidural analgesia during the entire continuum of labor and delivery
What is the current status of trial NCT01861821?
This trial is currently completed. It is a NA study. The enrollment target is 650 participants. The study started on 2011-11. Estimated completion is 2013-06.
What interventions are being tested in trial NCT01861821?
The interventions under investigation include: Multiport flexible catheter (DEVICE), Uniport flexible catheter (DEVICE).
Who is sponsoring clinical trial NCT01861821?
This trial is sponsored by Baylor Research Institute, which has 180 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01861821's enrollment target sits among peer trials
650 156th of 2000 higher than 1,845 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT02934477 · 650 participants
Prospective Assessment of Allogeneic Hematopoietic Cell Transplantation in Patients With Myelofibrosis
- NCT04579120 · 650 participants
Neuroimaging in Healthy Aging and Senile Dementia (HASD_IND)
- NCT04875702 · 650 participants · Phase 4
Treat-to-Target Serum Urate Versus Treat-to-Avoid Symptoms in Gout
- NCT05046600 · 650 participants
Registry of Arthrex Hand and Wrist Products
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia