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NCT04036968 · ClinicalTrials.gov registry record · Phase 2

Enhancing Medication-based Analgesia in Humans- STUDY 2

A Phase 2 study, sponsored by Johns Hopkins University.

Completed
Registry status
Phase 2
Development phase
31
Enrollment target

NCT04036968: Completed Phase 2 study, sponsored by Johns Hopkins University.

NCT04036968 is a Phase 2 study that has completed, run by Johns Hopkins University. The registered enrollment target is 31 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04036968, a Phase 2 study, has completed, sponsored by Johns Hopkins University.

COMPLETED
Registry status
Phase 2
Development phase
31 participants
Enrollment target

Study Summary

This is a single-group, within-subject, double-blind, double-dummy, placebo and active-controlled study evaluated whether the FDA-approved cannabinoid cannabidiol (CBD; Epidiolex) would enhance analgesia, subjective reports, and cognitive performance when compared to the FDA-approved opioid hydromorphone (Dilaudid). This is study 2 is a series of studies.

Interventions

  • DRUG Within-subject test of blinded study medications

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2020-02-01
Est. Completion 2022-11-01
Phase Phase 2

Sponsor

Johns Hopkins University

1,448 total trials

What the Registry Record Tells You About NCT04036968

The ClinicalTrials.gov registry entry for NCT04036968 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Within-subject test of blinded study medications is the first listed.

NCT04036968 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04036968 about?

NCT04036968 is a clinical study titled "Enhancing Medication-based Analgesia in Humans- STUDY 2". This is a single-group, within-subject, double-blind, double-dummy, placebo and active-controlled study evaluated whether the FDA-approved cannabinoid cannabidiol (CBD; Epidiolex) would enhance analgesia, subjective reports, and cognitive performance when compared to the FDA-approved opioid hydromor...

What is the current status of trial NCT04036968?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 31 participants. The study started on 2020-02-01. Estimated completion is 2022-11-01.

What interventions are being tested in trial NCT04036968?

The interventions under investigation include: Within-subject test of blinded study medications (DRUG).

Who is sponsoring clinical trial NCT04036968?

This trial is sponsored by Johns Hopkins University, which has 1,448 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, the data changelog, or report a data error.