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Remimazolam Tosilate Sedation and Midazolam Sedation in Dental Patients

The Effects of Remimazolam Tosilate Sedation Compared With Midazolam Sedation in Dental Patients: A Double Blind, Prospective , Randomized Controlled Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04602845
Enrollment
81
Registered
2020-10-26
Start date
2021-04-01
Completion date
2021-12-31
Last updated
2022-03-15

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

Conditions

Midazolam, Remimazolam, Sedation Complication

Keywords

Remimazolam, Midazolam, Sedation

Brief summary

Remimazolam Tosilate is a new short-acting benzodiazepines used in sedation. It has the advantages of rapid metabolism, quick recovery without injection pain. This study aims to compared with Midazolam, study whether Remimazolam Tosilate can achieve the same sedation effect with lower side effects on sedation maintenance period, During the recovery period of anesthesia, can Remimazolam Tosilatebe more stable and rapid.

Interventions

DRUGFentanyl

50ug Fentanyl intravenously

DRUGFlurbiprofen

50mg Fentanyl intravenously

DRUGMidazolam

2.5mg midazolam in 2ml normal saline intravenously

DRUGRemimazolam

3mg Remimazolam in 2ml normal saline intravenously

Sponsors

Peking University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

1. Age 18-60 2. BMI in 18-30Kg / m2 3. ASA classification I-II level 4. Sign informed consent 5. Patients whose outpatient treatment time less than 1 hour 6. The methods of local anesthesia including: periosteum infiltration method, periodontal ligament injection method, regional nerve block method

Exclusion criteria

1. Patients who are allergic to benzodiazepines, opioids, flumazenil or have contraindications 2. Long-term use of benzodiazepines 3. Long-term use of opioids 4. Participate in other clinical trials within 4 weeks 5. Women during pregnancy or breastfeeding 6. Patients who have a history of drug abuse or long-term alcohol abuse 7. Patients who suffer from mental illness or unable to cooperate with the experiment

Design outcomes

Primary

MeasureTime frameDescription
Success rates of sedationDay 0Success rates for patients who completed outpatient treatment with sufficient depth of sedation, additional sedation medication less than 5 times /15 minutes, and without the need of propofol for further sedation.

Secondary

MeasureTime frameDescription
Time to reach ideal sedationDay 0Time to reach Modified Observer Assessment of Sedation Score (MOAA/S) ≤ 3 after drug administration
Differences in blood pressure between the two groupsDay 0Differences in blood pressure during the operation between the two groups
Differences in heart rate between the two groupsDay 0Differences in heart rate during the operation between the two groups
Differences in basic vital signs between the two groupsDay 0Differences in blood pressure, heart rate, and BIS at different points during the operation between the two groups
Deepest sedation of MOAA/SDay 0The lowest intraoperative sedation depth of MOAA/S
Deepest sedation of Bispect ral index(BIS) valueDay 0The lowest intraoperative sedation depth of BIS value
Recovery of orientationDay 0Time from the end of the treatment to the recovery of orientation
Benzodiazepine dosageDay 0Intraoperative benzodiazepine dosage
Respiratory complication occurrence rateDay 0Respiratory complication including: intraoperative hypoxemia, respiratory depression and other complications in the two groups.
Discharge timeDay 0Time to be allowed to discharge after finishing the treatment
The Hopkins Language Learning Test scoreDay 0The Hopkins Language Learning Test (HVLT-R) score 15 minutes after the end the of the treatment. HVLT-R is a assessment of the patients' language learning condition , this score is from 0 to 30, the more score patients get means the better of patients' Language Learning condition.
Usage rate of flumazenilDay 0If the patients' MOAA/S less than 4 for more than 15 minutes, flumazenil will be used. The usage rate of flumazenil is the number of patients use flumazenil/ the number of all patients.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026