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Comparison of Emergence/Dysphoric Reaction Frequency of Using 2 Different Doses Ketamine

NCT05786365 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 108

Last updated 2024-07-30

No results posted yet for this study

Summary

The aim of this study is to compare the effect of using different doses of ketamine on producing dysphoric reaction.

Conditions

  • Sedation Complication

Interventions

DRUG

Ketalar 50 MG/ML Injectable Solution

Ketamine will be administered to two different groups as 0.5 mg/kg and 1 mg/kg

Sponsors & Collaborators

  • Aksaray University Training and Research Hospital

    lead OTHER

Principal Investigators

  • Kamil Kokulu, M.D. · Aksaray UTRH

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-01
Primary Completion
2023-09-15
Completion
2023-12-31
FDA Drug
Yes

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT05786365 on ClinicalTrials.gov