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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

A Study to Investigate the Pharmacokinetics of Midazolam After Repeated Doses of Camizestrant (AZD9833) and to Investigate the Pharmacokinetics of Camizestrant When Administered Alone and in Combination With Carbamazepine in Healthy Post-Menopausal Female Participants

Phase 1
Recruiting
Conditions
Healthy Participants
Interventions
First Posted Date
2024-08-09
Last Posted Date
2025-04-01
Lead Sponsor
AstraZeneca
Target Recruit Count
40
Registration Number
NCT06547164
Locations
🇬🇧

Research Site, Harrow, United Kingdom

A Drug-drug Interaction Study Evaluating the Perpetrator Potential of LY4100511 (DC-853) on Midazolam, Repaglinide, Digoxin, Rosuvastatin in Healthy Participants

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: LY4100511 (DC-853) Dose 1
Drug: LY4100511 (DC-853) Dose 2
Drug: LY4100511 (DC-853) Dose 3
First Posted Date
2024-07-16
Last Posted Date
2025-01-24
Lead Sponsor
DICE Therapeutics, Inc., a wholly owned subsidiary of Eli Lilly and Company
Target Recruit Count
49
Registration Number
NCT06503679
Locations
🇺🇸

Fortrea Clinical Research Unit, Dallas, Texas, United States

Ketamine for Methamphetamine Use Disorder

Phase 2
Recruiting
Conditions
Substance Use
Substance Use Disorders
Methamphetamine Abuse
Interventions
First Posted Date
2024-07-11
Last Posted Date
2025-04-27
Lead Sponsor
University of Texas Southwestern Medical Center
Target Recruit Count
120
Registration Number
NCT06496750
Locations
🇺🇸

Addiction Institute of Mount Sinai, New York, New York, United States

🇺🇸

Interdisciplinary Substance Use and Brain Injury Facility, Albuquerque, New Mexico, United States

🇺🇸

Prisma Health, Greenville, South Carolina, United States

and more 1 locations

A Study in Healthy Men to Test Whether Zongertinib Affects How 3 Other Medicines (Midazolam, Omeprazole, and Repaglinide) Are Taken up and Processed by the Body

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2024-07-10
Last Posted Date
2024-11-13
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
16
Registration Number
NCT06494761
Locations
🇩🇪

Humanpharmakologisches Zentrum Biberach, Biberach, Germany

I-CBT and IV Ketamine for Suicidality in Treatment-Resistant Depression: a Randomized, Midazolam-Controlled Clinical Trial

Phase 2
Recruiting
Conditions
Major Depressive Disorder
Suicide
Treatment Resistant Depression
Interventions
Behavioral: i-CBT (Internet-based Cognitive Behavioural Therapy)
First Posted Date
2024-06-28
Last Posted Date
2025-04-01
Lead Sponsor
University Health Network, Toronto
Target Recruit Count
110
Registration Number
NCT06480500
Locations
🇨🇦

Toronto General Hospital, Toronto, Ontario, Canada

🇨🇦

Ontario Shores Centre for Mental Health Sciences, Whitby, Ontario, Canada

Comparison of Intravenous V/S Nasal Atomizer Delivery of Midazolam for Conscious Sedation for No-scalpel Vasectomy

Phase 4
Completed
Conditions
Vasectomy
Sedation
Interventions
Device: midazolam by nasal atomizer
First Posted Date
2024-06-10
Last Posted Date
2024-06-10
Lead Sponsor
University of Tennessee Graduate School of Medicine
Target Recruit Count
35
Registration Number
NCT06449365
Locations
🇺🇸

UTGSM, Knoxville, Tennessee, United States

Intranasal Dexmedetomidine Versus Oral Midazolam Premedication for Postoperative Negative Behavior Changes in Children

Phase 4
Recruiting
Conditions
Behavior Problem
Interventions
Drug: normal Saline
Drug: Glucose solution
First Posted Date
2024-05-16
Last Posted Date
2024-08-16
Lead Sponsor
Fujian Provincial Hospital
Target Recruit Count
324
Registration Number
NCT06417125
Locations
🇨🇳

Fujian Provincial Hospital, Fuzhou, Fujian, China

Preoperative Oral Midazolam to Postoperative Pain Relief in Sleep Disturbance or Anxiety Patients With Colorectal Cancer

Not Applicable
Recruiting
Conditions
Preoperative
Midazolam
Sleep Disturbance
Anxiety
Pain, Postoperative
Interventions
First Posted Date
2024-05-09
Last Posted Date
2025-04-06
Lead Sponsor
Sixth Affiliated Hospital, Sun Yat-sen University
Target Recruit Count
280
Registration Number
NCT06407518
Locations
🇨🇳

the Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China

A Phase 1, Open-label Study Evaluating the Pharmacokinetics and Drug-drug Interaction of VX-993 in Healthy Adults

Phase 1
Completed
Conditions
Pain
Interventions
First Posted Date
2024-04-30
Last Posted Date
2024-08-01
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Target Recruit Count
42
Registration Number
NCT06392659
Locations
🇬🇧

MAC Clinical Research, Manchester, United Kingdom

The Efficacy of Thoracic Erector Spinae Plane Block For Perioperative Analgesia in Laparoscopic Bariatric Surgery for Super Obese Patients.

Not Applicable
Recruiting
Conditions
Super Obese Patients
Erector Spinae Plane Block
Bariatric Surgery
Interventions
Procedure: ESPB
Procedure: local anaesthetic infiltration
First Posted Date
2024-04-22
Last Posted Date
2025-04-30
Lead Sponsor
Amany Ahmed Eissa
Target Recruit Count
60
Registration Number
NCT06377605
Locations
🇪🇬

Kasr Al Ainy Hospitals, Cairo, Egypt

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