MedPath

Midazolam

Generic Name
Midazolam
Brand Names
Buccolam, Busulfex, Nayzilam, Seizalam
Drug Type
Small Molecule
Chemical Formula
C18H13ClFN3
CAS Number
59467-70-8
Unique Ingredient Identifier
R60L0SM5BC
Background

Midazolam is a short-acting hypnotic-sedative drug with anxiolytic, muscle relaxant, anticonvulsant, sedative, hypnotic, and amnesic properties. It belongs to a class of drugs called benzodiazepines. This drug is unique from others in this class due to its rapid onset of effects and short duration of action. Midazolam is available by oral, rectal, intranasal, intramuscular (IM), and intravenous (IV) routes and has been used in various biomedical applications, including dentistry, cardiac surgery, and endoscopic procedures as pre-anesthetic medication, and as an adjunct to local anesthesia.

This drug was initially approved by the US FDA in 1985, and has been approved for various indications since. In late 2018, the intramuscular preparation was approved by the FDA for the treatment of status epilepticus in adults. In May 2019, the nasal spray of midazolam was approved for the acute treatment of distinctive intermittent, stereotypic seizure episodes in patients 12 years of age and older. Midazolam is considered a schedule IV drug in the United States due to the low potential for abuse and low risk of dependence.

Indication

Midazolam has different indications depending on its formulation by the FDA.

Nasal

For the nasal spray formulation, midazolam is indicated for the acute treatment of intermittent, stereotypic episodes of frequent seizure activity (i.e., seizure clusters, acute repetitive seizures) that are distinct from a patient’s usual seizure pattern in patients with epilepsy 12 years of age and older.

Intravenous

For the intravenous injection formulation, midazolam is indicated as an agent for sedation/anxiolysis/amnesia and prior to or during diagnostic, therapeutic or endoscopic procedures, such as bronchoscopy, gastroscopy, cystoscopy, coronary angiography, cardiac catheterization, oncology procedures, radiologic procedures, suture of lacerations and other procedures either alone or in combination with other CNS depressants. The sedative, anxiolytic and amnestic use of midazolam can also be employed pre-operatively. It can also be indicated for induction of general anesthesia, before administration of other anesthetic agents or as a component of intravenous supplementation of nitrous oxide and oxygen for a balanced anesthesia. A relatively narrower dose range of midazolam and a shorter period of induction can be achieved if midazolam is combined with narcotic premedication. Finally, midazolam can be indicated as a continous intravenous infusion for sedation of intubated and mechanically ventilated patients as a component of anesthesia or during treatment in a critical care setting.

Intramuscular

For the intramusuclar injection formulation, midazolam is indicated for preoperative sedation/anxiolysis/amnesia or for treatment of status epilepticus in adults.

Oral

Midazolam syrup is indicated for use in pediatric patients for sedation, anxiolysis and amnesia prior to diagnostic, therapeutic or endoscopic procedures or before induction of anesthesia. It is only approved in monitored settings only and not for chronic or home use.

In Europe, a buccal formulation of midazolam is also approved for the treatment of prolonged, acute, convulsive seizures in infants, toddlers, children and adolescents (from 3 months to < 18 years). For infants between 3-6 months of age treatment should be in a hospital setting where monitoring is possible and resuscitation equipment is available.

Associated Conditions
Epileptic seizure, Status Epilepticus
Associated Therapies
Anaesthesia, Anxiolytic therapy therapy, Sedation for mechanically-ventilated patients, Preoperative amnesia therapy, Preoperative sedation therapy

This Study Tests the Effect of Risankizumab on the Metabolism in the Liver of Five Additional Drugs to Study Possible Drug Interactions in Patients With Psoriasis With or Without Psoriatic Arthritis

First Posted Date
2016-05-13
Last Posted Date
2017-09-25
Lead Sponsor
AbbVie
Target Recruit Count
21
Registration Number
NCT02772601
Locations
🇩🇪

Boehringer Ingelheim Investigational Site, Berlin, Germany

Phase 4, Vedolizumab-4002 Post-marketing, Disease-Drug-Drug Interaction Study

Phase 4
Withdrawn
Conditions
Colitis, Ulcerative
Crohn Disease
Interventions
First Posted Date
2016-05-03
Last Posted Date
2020-10-27
Lead Sponsor
Takeda
Registration Number
NCT02760615
Locations
🇺🇸

WCCT, Cypress, California, United States

🇺🇸

QPS MRA, Miami, Florida, United States

A Phase I Study With LEO 32731 and Midazolam in Healthy Male Subjects

Phase 1
Terminated
Conditions
Psoriasis Vulgaris
Interventions
Drug: Midazolam
Drug: LEO 32731
First Posted Date
2016-04-27
Last Posted Date
2017-05-03
Lead Sponsor
LEO Pharma
Target Recruit Count
12
Registration Number
NCT02753218
Locations
🇬🇧

Covance Clinical Research Unit Ltd., Springfield House, Hyde Street, Leeds, United Kingdom

Pharmacokinetic Drug-Drug Interaction Study of Rucaparib

First Posted Date
2016-04-15
Last Posted Date
2023-06-09
Lead Sponsor
pharmaand GmbH
Target Recruit Count
17
Registration Number
NCT02740712
Locations
🇵🇱

BioVirtus Research Site, Kajetany, Mokra 7, Poland

🇵🇱

Zachodniopomorskie Centrum Onkologii Centrum Innowacji, Szczecin, Poland

🇵🇱

Med Polonia, Poznan, Poland

Intensive 7-day Treatment for PTSD Combining Ketamine With Exposure Therapy

Phase 2
Terminated
Conditions
Posttraumatic Stress Disorder
Interventions
First Posted Date
2016-04-05
Last Posted Date
2022-10-17
Lead Sponsor
Yale University
Target Recruit Count
28
Registration Number
NCT02727998
Locations
🇺🇸

Yale University School of Medicine, New Haven, Connecticut, United States

Phase 1 Study to Determine the Effect of Lenvatinib (E7080) on the Pharmacokinetics of Midazolam in Subjects With Advanced Solid Tumors

Phase 1
Completed
Conditions
Tumors
Interventions
First Posted Date
2016-02-19
Last Posted Date
2019-08-28
Lead Sponsor
Eisai Inc.
Target Recruit Count
51
Registration Number
NCT02686164
Locations
🇺🇸

Facility # 1, San Antonio, Texas, United States

The Platelet Aggregation After tiCagrelor Inhibition and FentanYl Trial (PACIFY)

Phase 4
Completed
Conditions
Coronary Artery Disease
Interventions
Drug: Fentanyl
Other: Removal of Fentanyl from peri-procedural analgesia
Drug: Lidocaine
Drug: Midazolam
First Posted Date
2016-02-17
Last Posted Date
2018-06-07
Lead Sponsor
Johns Hopkins University
Target Recruit Count
212
Registration Number
NCT02683707
Locations
🇺🇸

Johns Hopkins Hospital and University School of Medicicine, Baltimore, Maryland, United States

Ketamine for Relapse Prevention in Recurrent Depressive Disorder

Phase 1
Terminated
Conditions
Depression
Recurrent Depressive Disorder
Relapse
Major Depressive Disorder
Interventions
First Posted Date
2016-01-22
Last Posted Date
2020-01-13
Lead Sponsor
St Patrick's Hospital, Ireland
Target Recruit Count
9
Registration Number
NCT02661061
Locations
🇮🇪

St Patrick's University Hospital, Dublin, Ireland

Effects of Systemic or Adjunct Tramadol Addition to Lidocaine Used for IVRA in Patients Undergoing Hand Surgery

Phase 3
Completed
Conditions
Anesthesia
Interventions
First Posted Date
2016-01-20
Last Posted Date
2016-01-20
Lead Sponsor
Bagcilar Training and Research Hospital
Target Recruit Count
60
Registration Number
NCT02658721

A Study of GDC-0134 to Determine Initial Safety, Tolerability, and Pharmacokinetic Parameters in Participants With Amyotrophic Lateral Sclerosis

Phase 1
Completed
Conditions
Amyotrophic Lateral Sclerosis
Interventions
First Posted Date
2016-01-14
Last Posted Date
2020-08-06
Lead Sponsor
Genentech, Inc.
Target Recruit Count
54
Registration Number
NCT02655614
Locations
🇺🇸

Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

🇺🇸

Mayo Clinic Hospital - Florida, Jacksonville, Florida, United States

🇺🇸

Forbes Norris Mda/als Ctr; Research Center, San Francisco, California, United States

and more 7 locations
© Copyright 2025. All Rights Reserved by MedPath