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NCT04992572 · ClinicalTrials.gov registry record · Early Phase 1

Study Comparing Local/ MAC Anesthesia in Lumbar Decompression

A Early Phase 1 study of Lumbar Spinal Stenosis, sponsored by Stanford University.

Recruiting
Registry status
Early Phase 1
Development phase
100
Enrollment target
2
Study locations

NCT04992572 is a Early Phase 1 study of Lumbar Spinal Stenosis that is actively recruiting participants, run by Stanford University. The registered enrollment target is 100 participants, below the 664-participant average among 18 other Lumbar Spinal Stenosis trials with a reported enrollment target (85% lower). The trial reports 2 study locations across 1 state.

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The verdict

NCT04992572, a Early Phase 1 study of Lumbar Spinal Stenosis, is actively recruiting participants, sponsored by Stanford University.

RECRUITING
Registry status
Early Phase 1
Development phase
100 participants
Enrollment target
2
Study locations

Study Summary

Explore efficacy, complications, and other factors associated with anaesthetic choice- To evaluate the efficacy of local + MAC as an alternative anesthetic to general anesthesia and to analyze patients' outcomes and experiences.

Conditions Studied

Lumbar Spinal Stenosis

Interventions

  • DRUG Propofol Injection
  • DRUG Lidocaine Hydrochloride, Injectable

Study Locations (2)

California

  • Outpatient Surgery Center/Stanford Spine Clinic - Redwood City
  • Stanford Outpatient surgery center - Redwood City

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2021-12-01
Est. Completion 2028-12-31
Phase Early Phase 1

Sponsor

Stanford University

1,744 total trials

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What the Registry Record Tells You About NCT04992572

The ClinicalTrials.gov registry entry for NCT04992572 describes a study currently listed as recruiting, categorized as Early Phase 1. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 664-participant average among 18 other Lumbar Spinal Stenosis trials with a reported enrollment target (85% lower). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Lumbar Spinal Stenosis appearing as the primary indexed condition, and to 2 interventions - of which Propofol Injection is the first listed.

NCT04992572 reports 2 study locations spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT04992572 about?

NCT04992572 is a clinical study titled "Study Comparing Local/ MAC Anesthesia in Lumbar Decompression". Explore efficacy, complications, and other factors associated with anaesthetic choice- To evaluate the efficacy of local + MAC as an alternative anesthetic to general anesthesia and to analyze patients' outcomes and experiences.

What is the current status of trial NCT04992572?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 100 participants. The study started on 2021-12-01. Estimated completion is 2028-12-31.

What conditions does trial NCT04992572 study?

This clinical trial studies the following conditions: Lumbar Spinal Stenosis.

What interventions are being tested in trial NCT04992572?

The interventions under investigation include: Propofol Injection (DRUG), Lidocaine Hydrochloride, Injectable (DRUG).

Who is sponsoring clinical trial NCT04992572?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04992572 being conducted?

This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.