Skip to content

Comparison of remimazolam and midazolam administration in ketamin infusion therapy for chronic pain patients

Comparison of remimazolam and midazolam administration in ketamin infusion therapy for chronic pain patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008955
Enrollment
62
Registered
2023-11-15
Start date
2022-08-19
Completion date
Unknown
Last updated
2023-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : 1) Research Method Overview To perform sedative treatment with ketamine and remimazolam or midazolam, the patient visits the hospital after fasting for more than 8 hours. Before sedation treatm

Sponsors

Konkuk University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) a target disease Chronic pain diseases subject to sedative treatment using ketamine, such as "complex regional pain syndrome," "fiber muscle pain," and "neuropathic pain." 2) Selection criteria and exclusion criteria of study subjects - Patients who are being treated for chronic pain for more than 6 months - Patients with neuropathic pain or fibromyalgia - Patients who agree with the study process

Exclusion criteria

Exclusion criteria: - Patients who are hypersensitive or allergic to ketamine, remimazolam, and midazolam - Drugs or alcoholics - Patients with heart disease such as angina, arrhythmia, and heart failure - Pregnant or potentially pregnant patients - Patients who disagree with the study

Design outcomes

Primary

MeasureTime frame
pain severity

Secondary

MeasureTime frame
side effects

Countries

Korea, Republic of

Contacts

Public ContactJae Hun Kim

Konkuk University Medical Center

painfree@kuh.ac.kr+82-2-2030-5749

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026