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NCT03173326 · ClinicalTrials.gov registry record · NA

Patient Satisfaction and Postoperative Analgesia Between Subarachnoid Block With 2-chloroprocaine Versus General Anesthesia for Knee Arthroscopy

A NA study, sponsored by Vanderbilt University Medical Center.

Terminated
Registry status
NA
Development phase
1
Enrollment target

NCT03173326 is a NA study that was terminated before completion, run by Vanderbilt University Medical Center. The registered enrollment target is 1 participants.

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The verdict

NCT03173326, a NA study, was terminated before completion, sponsored by Vanderbilt University Medical Center.

TERMINATED
Registry status
NA
Development phase
1 participants
Enrollment target

Study Summary

The study evaluates the efficacy of two different anesthetic techniques in patients undergoing unilateral knee arthroscopy. Participants will be randomized to receive either subarachnoid block with 2-chloroprocaine or general anesthesia plus intravenous fentanyl.

Interventions

  • PROCEDURE General anesthesia
  • PROCEDURE Subarachnoid block

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2017-06-16
Est. Completion 2018-04-20
Phase NA

What the Registry Record Tells You About NCT03173326

The ClinicalTrials.gov registry entry for NCT03173326 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 1 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which General anesthesia is the first listed.

NCT03173326 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03173326 about?

NCT03173326 is a clinical study titled "Patient Satisfaction and Postoperative Analgesia Between Subarachnoid Block With 2-chloroprocaine Versus General Anesthesia for Knee Arthroscopy". The study evaluates the efficacy of two different anesthetic techniques in patients undergoing unilateral knee arthroscopy. Participants will be randomized to receive either subarachnoid block with 2-chloroprocaine or general anesthesia plus intravenous fentanyl.

What is the current status of trial NCT03173326?

This trial is currently terminated. It is a NA study. The enrollment target is 1 participants. The study started on 2017-06-16. Estimated completion is 2018-04-20.

What interventions are being tested in trial NCT03173326?

The interventions under investigation include: General anesthesia (PROCEDURE), Subarachnoid block (PROCEDURE).

Who is sponsoring clinical trial NCT03173326?

This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.

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

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.