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NCT04849455 · ClinicalTrials.gov registry record · Phase 4

Erector Spinae Plane Block Catheters and Intrathecal Morphine for Hepatic Resection

A Phase 4 study of Anesthesia and Acute Pain, sponsored by University of California, San Diego.

Recruiting
Registry status
Phase 4
Development phase
70
Enrollment target
1
Study location

NCT04849455 is a Phase 4 study of Anesthesia and Acute Pain that is actively recruiting participants, run by University of California, San Diego. The registered enrollment target is 70 participants, below the 109,409-participant average among 57 other Anesthesia trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04849455, a Phase 4 study of Anesthesia and Acute Pain, is actively recruiting participants, sponsored by University of California, San Diego.

RECRUITING
Registry status
Phase 4
Development phase
70 participants
Enrollment target
1
Study location

Study Summary

To determine whether the addition of erector spinae plane (ESP) catheters to existing multimodal analgesic regimen with intrathecal morphine provides superior postoperative analgesia in patients undergoing hepatic resection compared with patients not receiving ESP catheters.

Interventions

  • DRUG 0.2% ropivacaine local anesthetic continuous erector spinae plane block
  • DRUG 0.2% ropivacaine local anesthetic superficially taped continuous erector spinae plane block
  • DRUG Spinal Morphine

Study Locations (1)

California

  • University of California, San Diego - San Diego

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2021-05-24
Est. Completion 2023-05-01
Phase Phase 4

Sponsor

University of California, San Diego

775 total trials

What the Registry Record Tells You About NCT04849455

The ClinicalTrials.gov registry entry for NCT04849455 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 109,409-participant average among 57 other Anesthesia trials with a reported enrollment target (100% lower). The listed sponsor is University of California, San Diego, which has 775 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Anesthesia appearing as the primary indexed condition, and to 3 interventions - of which 0.2% ropivacaine local anesthetic continuous erector spinae plane block is the first listed.

NCT04849455 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT04849455 about?

NCT04849455 is a clinical study titled "Erector Spinae Plane Block Catheters and Intrathecal Morphine for Hepatic Resection". To determine whether the addition of erector spinae plane (ESP) catheters to existing multimodal analgesic regimen with intrathecal morphine provides superior postoperative analgesia in patients undergoing hepatic resection compared with patients not receiving ESP catheters.

What is the current status of trial NCT04849455?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 70 participants. The study started on 2021-05-24. Estimated completion is 2023-05-01.

What conditions does trial NCT04849455 study?

This clinical trial studies the following conditions: Anesthesia, Acute Pain, Anesthesia, Local, Hepatic Resection.

What interventions are being tested in trial NCT04849455?

The interventions under investigation include: 0.2% ropivacaine local anesthetic continuous erector spinae plane block (DRUG), 0.2% ropivacaine local anesthetic superficially taped continuous erector spinae plane block (DRUG), Spinal Morphine (DRUG).

Who is sponsoring clinical trial NCT04849455?

This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04849455 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.