Stomach NeoplasmNCT06563063
Finding ED90 of Flumazenil for Selective Improvement of Respiratory Distress by Remimazolam
A study testing Flumazenil in people with Stomach Neoplasm, run by Yonsei University at 1 site in South Korea.
Trial summary
Patients undergoing endoscopic submucosal dissection with monitored anesthesia care (MAC) using remimazolam may develop respiratory distress during the procedure. In these cases, substandard doses of flumazenil have been found to improve respiratory distress without completely reversing sedation, a novel and… Read more about this study
- Who is it for?
- Ages 19 years and olderHealthy volunteers can take part
- Conditions the study is for
- Stomach Neoplasm
- What is being tested?
- Flumazenil
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteSouth Korea
- Study dates
- 23 Aug 2023to 1 Dec 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 19 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- American Society of Anesthesiologists (ASA) class I-III
- 19 years of age or older
- Scheduled for gastric ESD by MAC with remimazolam
- Hemodynamically stable patients.
Who cannot join
- Patients who have airway-related anatomic abnormalities
- Being requested by the endoscopist to be fully awake from anesthesia for any reason other than respiroatyr distress during the procedure
- Being administered any sedative other than remimazolam during the procedure (e.g., propofol, dexmedetomidine, etc.)
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Exploring the ED90 Capacity of Plumazenyl for the Improvement of Respiratory Deterioration During Anesthesia Management Under Monitoring Using Remimazolam - Prospective Study
Patients undergoing endoscopic submucosal dissection with monitored anesthesia care (MAC) using remimazolam may develop respiratory distress during the procedure. In these cases, substandard doses of flumazenil have been found to improve respiratory distress without completely reversing sedation, a novel and previously unknown phenomenon. This study aimed to explore the ED90 of flumazenil to selectively improve only respiratory distress during MAC with remimazolam.
The dose determination for flumazenil will follow a biased-coin up-and-down design. Starting with an initial dose of 5 mcg, if there is an improvement in respiratory distress, the biased-coin method will be used to administer the same dose to the next patient with a probability of 8/9, and a decreased dose of 5 mcg to the next patient with a probability of 1/9. Any improvement in respiratory distress within 30 seconds of flumazenil administration will be recorded. After the procedure, the patient will be asked if they had any memory recall of the procedure. Centered isotonic regression will be used to obtain the ED90 of flumazenil.
Read the detailed description
Study patients will be patients scheduled for ESD in our gastroenterology department, and blood pressure and pulse measured in the pre-procedure room will be considered baseline vital signs. At the start of the ESD procedure, MAC with remimazolam will be performed. A bolus of 5 mcg of remimazolam is given over 1 minute at the onset of sedation, followed by a continuous intravenous infusion of remimazolam at a rate of 0.1 to 0.4 mg/kg/hr during the procedure with a goal of a Modified Observer's Assessment of Alertness/Sedation Scale (MOAA/S) score of 2-3. Record the total amount of remimazolam infused during the procedure. For pain control during the procedure, administer 50 ug of fentanyl at baseline and an additional 25 ug bolus of fentanyl if the patient's blood pressure rises (>20% of baseline systolic blood pressure) or pulse rate increases (>20% of baseline heart rate) during the procedure, or if the patient moves. Enroll in the study if respiratory disturbance due to sedation overdose occurs during the procedure, resulting in 1) sustained hypoxia (SpO2 < 94%) with a risk of severe hypoxia, or 2) irregular breathing and excessive diaphragmatic breathing that prevents the endoscopist from performing the procedure. If no respiratory disturbances occur during the procedure, patients will be withdrawn from the study and excluded from statistical analysis. If any of the above respiratory disturbances occur, the remimazolam dose will remain unchanged and flumazenil will be administered to see if there is improvement. Improvement will be considered to occur if the respiratory disturbance resolves within 30 seconds, resulting in an increase in oxygen saturation and sustained to the point where endoscopy can be resumed. Dosing follows a biased-coin up-and-down design. Start with an initial dose of 5 mcg and increase by 5 mcg in the next patient if there is no respiratory improvement. If there is respiratory improvement, the same dose is given in the next patient with a probability of 8/9 and a probability of 1/9, using the biased-coin method, a 5 mcg decrease is given in the next patient. To determine the probability, the principal investigator will randomly generate a number from 1 to 9 using a random number generator, and if the randomly generated number is 1 to 8, the dose will be maintained, and if the number is 9, the dose will be reduced. The minimum dose will be 5 mcg and the maximum dose will be 150 mcg. If there is no respiratory improvement with the medication, start by reducing the remimazolam rate by 30%, attempting to establish an airway by elevating the jaw joint, and if respiratory distress persists, inserting a nasopharyngeal airway device. If respiratory distress improves, resume the procedure. After the procedure is completed, ask the patient if they are awake.
The study will follow a biased-coin up-and-down design, with 60 patients who developed respiratory disturbances during MAC with remimazolam for ESD as the final analysis population. The incidence of respiratory disturbances among patients undergoing MAC with remimazolam for ESD at our institution is about 40%, so 167 patients are needed, and we will apply the usual study dropout rate of 10% to target 167 patients undergoing MAC with remimazolam for ESD. However, if 60 patients develop respiratory distress before enrolling 167, and the study procedure is completed, the study will be terminated. The data from all 60 cases will then be used to find the ED90 using centered isotonic regression. Centered isotonic regression is a method of finding the proportion of patients who responded at each dose level and using this to obtain a cumulative distribution function of the proportion of patients who responded to the dose.17 This provides an estimate and confidence interval for the primary endpoint, the ED90 for improvement in respiratory impairment, and the probability of awakening, the secondary endpoint, at that ED90 dose, to assess the likelihood of during-procedure awakening at that ED90 dose.
- Conditions
- Stomach Neoplasm
- Being tested
- Flumazenil
- Keywords
- Monitored anesthesia care, sedation, endoscopic submucosal dissection
- Medical subject headings
- Stomach Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
FlumazenilDrug
The dose determination for flumazenil followed a biased-coin up-and-down design. Starting with an initial dose of 5 mcg, if there was an improvement in respiratory distress, the biased-coin method was used to give the same dose in the next patient with a probability of 8/9, and a decreased dose of 5 mcg in the next patient with a probability of 1/9.
| Study group | Role | What they receive |
|---|---|---|
| Flumazenil | Experimental | Not described Receives: Drug: Flumazenil |
What is being measured
The primary outcome is the main question the study is designed to answer.
Whether it was successful or unsuccessful to improve the patient's respiratory distress
Respiratory distress occurring during the procedure were defined as follows: 1) sustained hypoxia (SpO2 < 94%); or 2) excessive irregular breathing with heavy chest and abdominal movement, making it impossible for the endoscopist to perform the procedure. Improvement in respiratory distress was defined as recovery of hypoxia (SpO2 ≥ 95%) and improvement in respiratory pattern-loss of excessively irregular breathing and subdued chest and abdominal movement-within 30 seconds after flumazenil administration to the extent that the procedure could be resumed.
Measured: 30 seconds after the intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Aug 2024
- Study start23 Aug 2023
- Primary completion1 Dec 2023
- Study completion1 Dec 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Stomach NeoplasmStudies of the same condition, open and under way.
- More trials run by Yonsei UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Not applicable
- Intervention model
- Sequential
- Masking
- None (open label)
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Yonsei University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06563063
- Sponsor's protocol ID
- 4-2023-0507
- Status last verified
- Aug 2024
- First submitted
- 9 Aug 2024
- Last updated
- 20 Aug 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Aug 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Exploring the ED90 Capacity of Plumazenyl for the Improvement of Respiratory Deterioration During Anesthesia Management Under Monitoring Using Remimazolam - Prospective Study
- ClinicalTrials.gov ID
- NCT06563063
- Acronym / sponsor ID
- 4-2023-0507
- Conditions
- Stomach Neoplasm
- Keywords
- Monitored anesthesia care, sedation, endoscopic submucosal dissection
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Yonsei UniversityUniversity, hospital or other
- Study start
- 23 Aug 2023 (actual)
- Primary completion
- 1 Dec 2023 (actual)
- Study completion
- 1 Dec 2023 (actual)
- First posted
- 20 Aug 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Patients undergoing endoscopic submucosal dissection with monitored anesthesia care (MAC) using remimazolam may develop respiratory distress during the procedure. In these cases, substandard doses of flumazenil have been found to improve respiratory distress without completely reversing sedation, a novel and previously unknown phenomenon. This study aimed to explore the ED90 of flumazenil to selectively improve only respiratory distress during MAC with remimazolam.
The dose determination for flumazenil will follow a biased-coin up-and-down design. Starting with an initial dose of 5 mcg, if there is an improvement in respiratory distress, the biased-coin method will be used to administer the same dose to the next patient with a probability of 8/9, and a decreased dose of 5 mcg to the next patient with a probability of 1/9. Any improvement in respiratory distress within 30 seconds of flumazenil administration will be recorded. After the procedure, the patient will be asked if they had any memory recall of the procedure. Centered isotonic regression will be used to obtain the ED90 of flumazenil.
Detailed description
Study patients will be patients scheduled for ESD in our gastroenterology department, and blood pressure and pulse measured in the pre-procedure room will be considered baseline vital signs. At the start of the ESD procedure, MAC with remimazolam will be performed. A bolus of 5 mcg of remimazolam is given over 1 minute at the onset of sedation, followed by a continuous intravenous infusion of remimazolam at a rate of 0.1 to 0.4 mg/kg/hr during the procedure with a goal of a Modified Observer's Assessment of Alertness/Sedation Scale (MOAA/S) score of 2-3. Record the total amount of remimazolam infused during the procedure. For pain control during the procedure, administer 50 ug of fentanyl at baseline and an additional 25 ug bolus of fentanyl if the patient's blood pressure rises (>20% of baseline systolic blood pressure) or pulse rate increases (>20% of baseline heart rate) during the procedure, or if the patient moves. Enroll in the study if respiratory disturbance due to sedation overdose occurs during the procedure, resulting in 1) sustained hypoxia (SpO2 < 94%) with a risk of severe hypoxia, or 2) irregular breathing and excessive diaphragmatic breathing that prevents the endoscopist from performing the procedure. If no respiratory disturbances occur during the procedure, patients will be withdrawn from the study and excluded from statistical analysis. If any of the above respiratory disturbances occur, the remimazolam dose will remain unchanged and flumazenil will be administered to see if there is improvement. Improvement will be considered to occur if the respiratory disturbance resolves within 30 seconds, resulting in an increase in oxygen saturation and sustained to the point where endoscopy can be resumed. Dosing follows a biased-coin up-and-down design. Start with an initial dose of 5 mcg and increase by 5 mcg in the next patient if there is no respiratory improvement. If there is respiratory improvement, the same dose is given in the next patient with a probability of 8/9 and a probability of 1/9, using the biased-coin method, a 5 mcg decrease is given in the next patient. To determine the probability, the principal investigator will randomly generate a number from 1 to 9 using a random number generator, and if the randomly generated number is 1 to 8, the dose will be maintained, and if the number is 9, the dose will be reduced. The minimum dose will be 5 mcg and the maximum dose will be 150 mcg. If there is no respiratory improvement with the medication, start by reducing the remimazolam rate by 30%, attempting to establish an airway by elevating the jaw joint, and if respiratory distress persists, inserting a nasopharyngeal airway device. If respiratory distress improves, resume the procedure. After the procedure is completed, ask the patient if they are awake.
The study will follow a biased-coin up-and-down design, with 60 patients who developed respiratory disturbances during MAC with remimazolam for ESD as the final analysis population. The incidence of respiratory disturbances among patients undergoing MAC with remimazolam for ESD at our institution is about 40%, so 167 patients are needed, and we will apply the usual study dropout rate of 10% to target 167 patients undergoing MAC with remimazolam for ESD. However, if 60 patients develop respiratory distress before enrolling 167, and the study procedure is completed, the study will be terminated. The data from all 60 cases will then be used to find the ED90 using centered isotonic regression. Centered isotonic regression is a method of finding the proportion of patients who responded at each dose level and using this to obtain a cumulative distribution function of the proportion of patients who responded to the dose.17 This provides an estimate and confidence interval for the primary endpoint, the ED90 for improvement in respiratory impairment, and the probability of awakening, the secondary endpoint, at that ED90 dose, to assess the likelihood of during-procedure awakening at that ED90 dose.
Study design
- Primary purpose
- Supportive care
- Allocation
- Not applicable
- Intervention model
- Sequential
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Flumazenil | Experimental | Drug: Flumazenil |
Who may qualify
- Ages
- 19 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- American Society of Anesthesiologists (ASA) class I-III
- 19 years of age or older
- Scheduled for gastric ESD by MAC with remimazolam
- Hemodynamically stable patients.
Key exclusion criteria (3 listed)
- Patients who have airway-related anatomic abnormalities
- Being requested by the endoscopist to be fully awake from anesthesia for any reason other than respiroatyr distress during the procedure
- Being administered any sedative other than remimazolam during the procedure (e.g., propofol, dexmedetomidine, etc.)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| FlumazenilThe dose determination for flumazenil followed a biased-coin up-and-down design. Starting with an initial dose of 5 mcg, if there was an improvement in respiratory distress, the biased-coin method was used to give the same dose in the next patient with a probability of 8/9, and a decreased dose of 5 mcg in the next patient with a probability of 1/9. | Drug | Flumazenil |
Primary outcome
Whether it was successful or unsuccessful to improve the patient's respiratory distress
Time frame: 30 seconds after the intervention
Respiratory distress occurring during the procedure were defined as follows: 1) sustained hypoxia (SpO2 < 94%); or 2) excessive irregular breathing with heavy chest and abdominal movement, making it impossible for the endoscopist to perform the procedure. Improvement in respiratory distress was defined as recovery of hypoxia (SpO2 ≥ 95%) and improvement in respiratory pattern-loss of excessively irregular breathing and subdued chest and abdominal movement-within 30 seconds after flumazenil administration to the extent that the procedure could be resumed.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Aug 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Flumazenil in people with Stomach Neoplasm, run by Yonsei University at 1 site in South Korea.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 20 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Whether it was successful or unsuccessful to improve the patient's respiratory distress (time frame: 30 seconds after the intervention). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Aug 2024.