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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

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Phase 1
Recruiting
Conditions
Burns
Interventions
First Posted Date
2023-11-13
Last Posted Date
2024-02-01
Lead Sponsor
Ruijin Hospital
Target Recruit Count
32
Registration Number
NCT06126991
Locations
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Department of Burn, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, Shanghai, China

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Phase 3
Completed
Conditions
Tonsillectomy
Adenoidectomy
Drug-Related Side Effects and Adverse Reaction
Interventions
First Posted Date
2023-11-08
Last Posted Date
2024-10-14
Lead Sponsor
Kasr El Aini Hospital
Target Recruit Count
200
Registration Number
NCT06122948
Locations
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Cairo university hospitals, kasralainy, Cairo, Egypt

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Phase 1
Completed
Conditions
Chronic Obstructive Pulmonary Disease Exacerbation
COPD
Interventions
First Posted Date
2023-11-07
Last Posted Date
2024-02-28
Lead Sponsor
EpiEndo Pharmaceuticals
Target Recruit Count
37
Registration Number
NCT06118684
Locations
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Clinical Trial Consultants AB, Uppsala, Sweden

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Completed
Conditions
Bronchoscopy
Interventions
First Posted Date
2023-11-03
Last Posted Date
2024-01-31
Lead Sponsor
The Affiliated Hospital of Qingdao University
Target Recruit Count
424
Registration Number
NCT06116955
Locations
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Affiliated Hospital of Qingdao University, Shandong, Qingdao, China

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Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2023-11-01
Last Posted Date
2024-11-08
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
35
Registration Number
NCT06111521
Locations
🇺🇸

ICON Early Clinical & Bioanalytical Solutions, Salt Lake City, Utah, United States

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Phase 2
Completed
Conditions
Choledocholithiasis
Choledochal Cyst
Cholangitis
Pancreatic Cancer
Interventions
First Posted Date
2023-11-01
Last Posted Date
2025-03-25
Lead Sponsor
National University of Malaysia
Target Recruit Count
90
Registration Number
NCT06111872
Locations
🇲🇾

Hospital Canselor Tuanku Muhriz UKM, Cheras, Kuala Lumpur, Malaysia

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Phase 1
Active, not recruiting
Conditions
Healthy
Interventions
First Posted Date
2023-10-30
Last Posted Date
2024-06-26
Lead Sponsor
Pfizer
Target Recruit Count
110
Registration Number
NCT06106009
Locations
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Pfizer Clinical Research Unit - New Haven, New Haven, Connecticut, United States

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Phase 1
Completed
Conditions
Healthy Participants
Interventions
First Posted Date
2023-10-23
Last Posted Date
2024-01-11
Lead Sponsor
DICE Therapeutics, Inc., a wholly owned subsidiary of Eli Lilly and Company
Target Recruit Count
28
Registration Number
NCT06092931
Locations
🇺🇸

ICON Phase 1 Clinic, Salt Lake City, Utah, United States

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Phase 1
Not yet recruiting
Conditions
Alcohol Use Disorder
Depression
Interventions
First Posted Date
2023-10-19
Last Posted Date
2023-10-19
Lead Sponsor
University Hospital of North Norway
Target Recruit Count
34
Registration Number
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Phase 4
Not yet recruiting
Conditions
Postoperative Pain
Interventions
First Posted Date
2023-10-13
Last Posted Date
2023-10-16
Lead Sponsor
Assiut University
Target Recruit Count
90
Registration Number
NCT06082232
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