Trial · NCT03240055
The Effects of Spinal Anesthesia on ED50 and BIS50 of Etomidate for the Loss of Consciousness
NCT03240055, Not applicable, Completed, General Hospital of Ningxia Medical University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Effects of Spinal Anesthesia on ED50 and BIS50 of Etomidate for the Loss of Consciousness. Trials, record NCT03240055. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03240055
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Effects of Spinal Anesthesia on ED50 and BIS50 of Etomidate for the Loss of Consciousness
- NCT number
- NCT03240055
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 54 participants, actual
- Lead sponsor
- General Hospital of Ningxia Medical University
- Conditions
- Dose-Response Relationship, Drug
- Interventions
- spinal anesthesia, etomidate
- First posted
- 2017-08-04
- Last updated
- 2017-09-06
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Median effective dose (ED50)of etomidate at which 50% of patients lose consciousness | After etomidate administration to the lowest BIS value appears，usually about 4 minutes | We want to determine Median effective dose (ED50) of etomidate at which 50% of patients lose consciousness in the SE and E group, respectively. It is a value，like 0.105mg/kg. Patients were considered to be loss of consciousness if there Observer's Assessment of Alertness/Sedation (OAA/S) scores were 2,1,or 0. |
| Primary | BIS value (BIS50) of etomidate at which 50% of patients lose consciousness | After etomidate administration to the lowest BIS value appears，usually about 4 minutes | We want to determine BIS value (BIS50) of etomidate at which 50% of patients lose consciousness in the SE and E group, respectively. It is a unitless value，like 60. Patients were considered to be loss of consciousness if there Observer's Assessment of Alertness/Sedation (OAA/S) scores were 2,1,or 0. |
| Secondary | The change of Mean Arterial Pressure (MAP) | Baseline, l min (T1), 2min (T2), 3min (T3), 5min (T5) after administration of etomidate | |
| Secondary | The change of heart rate (HR) | Baseline, l min (T1), 2min (T2), 3min (T3), 5min (T5) after administration of etomidate |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03240055
GET https://conductscience.org/api/trials/v1/NCT03240055/registered