Trial · NCT02997800
The Effect of Intraoperative Labetalol on Time to Discharge
NCT02997800, Phase 2, Completed, Dr. Robert Tanzola
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Effect of Intraoperative Labetalol on Time to Discharge. Trials, record NCT02997800. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02997800
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Effect of Intraoperative Labetalol on Time to Discharge
- NCT number
- NCT02997800
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 172 participants, actual
- Lead sponsor
- Dr. Robert Tanzola
- Conditions
- Bloodpressure, Heart Rate
- Interventions
- Esmolol, Labetalol, Fentanyl, saline infusion, 1 ml saline infusion
- First posted
- 2016-12-20
- Last updated
- 2020-02-13
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Length of stay in the post-anesthesia care unit (PACU) | The time-frame between entry to PACU and discharge from PACU (approximately 1.5 hours). | time from arrival in PACU after surgery until discharge from PACU |
| Secondary | Intraoperative Heart Rate (HR) | intraoperatively-from anesthesia induction to the surgery completion (wound closure) -approximately 45 min. | heart rate (beats per min.) |
| Secondary | Intraoperative mean arterial pressure (MAP) | intraoperatively-from anesthesia induction to the surgery completion (wound closure)-approximately 45 min. | blood pressure (mmHg) |
| Secondary | postoperative nausea and vomiting (PONV) in PACU | The time-frame between entry to PACU and discharge from PACU (approximately 1.5 hours). | incidence of nausea and vomiting |
| Secondary | pain scores | The time-frame between entry to PACU and discharge from PACU (approximately 1.5 hours). | pain scores visual analogue scale (VAS) |
| Secondary | fentanyl required | The time-frame between entry to PACU and discharge from PACU (approximately 1.5 hours). | total fentanyl required mcg |
| Secondary | adverse effects | The time-frame between entry to PACU and discharge from PACU (approximately 1.5 hours). | Any reported adverse effects or complications |
| Secondary | postoperative heart rate | The time-frame between entry to PACU and discharge from PACU (approximately 1.5 hours). | heart rate (beats per min) |
| Secondary | postoperative mean arterial pressure (MAP) | The time-frame between entry to PACU and discharge from PACU (approximately 1.5 hours). | blood pressure (mmHg) |
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/NCT02997800
GET https://conductscience.org/api/trials/v1/NCT02997800/registered