Trial · NCT06063772
Effect of Treatment of Pre-induction Hypertension on Hemodynamic Stability During Induction of General Anesthesia
NCT06063772, Phase 4, Not yet recruiting, University of California, San Diego
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effect of Treatment of Pre-induction Hypertension on Hemodynamic Stability During Induction of General Anesthesia. Trials, record NCT06063772. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06063772
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effect of Treatment of Pre-induction Hypertension on Hemodynamic Stability During Induction of General Anesthesia
- NCT number
- NCT06063772
- Status
- Not yet recruiting
- Phases
- Phase 4
- Enrollment
- 64 participants, estimated
- Lead sponsor
- University of California, San Diego
- Conditions
- Hypertension
- Interventions
- Clevidipine, Lactated Ringers, Intravenous
- First posted
- 2023-10-03
- Last updated
- 2024-11-08
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Magnitude and Duration of Deviation from a normal blood pressure range. | The investigators will measure and record blood pressure at 2 minute intervals from induction of anesthesia until just prior to incision. | Blood pressure (systolic, diastolic and mean) will be recorded and plotted against time. The area under the curve of that plot that is outside of the normal blood pressure range is the outcome measure upon which the investigators will compare the clevidipine treated cohort to the placebo treated cohort. |
| Secondary | Dose of vasoactive drugs used during induction of anesthesia. | Investigators will record the dose of vasoactive drugs administered from induction until just prior to incision. | All vasoactive drug name(s) and dose (s) will be recorded. The difference in doses will be compared between the clevidipine cohort and the placebo cohort. |
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/NCT06063772
GET https://conductscience.org/api/trials/v1/NCT06063772/registered