Intranasal Esketamine to Maintain the Antidepressant Response to IV Racemic Ketamine

NCT04856124 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2021-04-23

No results posted yet for this study

Summary

This study aims to assess the efficacy and safety of intranasal esketamine as maintenance antidepressant therapy in patients who have demonstrated clinical improvement with off-label intravenous racemic ketamine for treatment-resistant depression.

Conditions

Interventions

DRUG

Intranasal esketamine

Subjects with a clinically meaningful response to IV racemic ketamine were switched to IN esketamine

Sponsors & Collaborators

  • Psych Atlanta

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-09-01
Primary Completion
2020-12-15
Completion
2021-03-01
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04856124 on ClinicalTrials.gov