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NCT04369950 · ClinicalTrials.gov registry record · Phase 4

Post-cesarean Analgesia With Epidural Morphine Following Epidural 2-chloroprocaine

A Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.

Completed
Registry status
Phase 4
Development phase
44
Enrollment target

NCT04369950: Completed Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.

NCT04369950 is a Phase 4 study that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 44 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04369950, a Phase 4 study, has completed, sponsored by The University of Texas Health Science Center, Houston.

COMPLETED
Registry status
Phase 4
Development phase
44 participants
Enrollment target

Study Summary

The purpose of this study is to show that the effect of 3% 2-chloroprocaine prior to epidural morphine administration will be not inferior to the effect of epidural 2% lidocaine with 1:200,000 epinephrine on total opioid use for 24h

Interventions

  • DRUG 2% lidocaine with 1:200,000 epinephrine and epidural morphine
  • DRUG 3% 2-chloroprocaine and epidural morphine

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2020-05-11
Est. Completion 2021-07-11
Phase Phase 4

What the finished NCT04369950 record still lists

NCT04369950 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 2 interventions - of which 2% lidocaine with 1:200,000 epinephrine and epidural morphine is the first listed.

NCT04369950 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04369950 about?

NCT04369950 is a clinical study titled "Post-cesarean Analgesia With Epidural Morphine Following Epidural 2-chloroprocaine". The purpose of this study is to show that the effect of 3% 2-chloroprocaine prior to epidural morphine administration will be not inferior to the effect of epidural 2% lidocaine with 1:200,000 epinephrine on total opioid use for 24h

What is the current status of trial NCT04369950?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 44 participants. The study started on 2020-05-11. Estimated completion is 2021-07-11.

What interventions are being tested in trial NCT04369950?

The interventions under investigation include: 2% lidocaine with 1:200,000 epinephrine and epidural morphine (DRUG), 3% 2-chloroprocaine and epidural morphine (DRUG).

Who is sponsoring clinical trial NCT04369950?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04369950's enrollment target sits among peer trials

44 1363rd of 2000 higher than 630 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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

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Source: ClinicalTrials.gov NCT04369950, the US trial registry maintained by the National Library of Medicine. NCT04369950 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.