Trial · NCT07895836
Multimodal Monitoring During General Anesthesia in ENT Surgery
NCT07895836, Not applicable, Completed, Barbara Verro
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Multimodal Monitoring During General Anesthesia in ENT Surgery. Trials, record NCT07895836. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07895836
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Multimodal Monitoring During General Anesthesia in ENT Surgery
- NCT number
- NCT07895836
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 200 participants, actual
- Lead sponsor
- Barbara Verro
- Conditions
- General Anesthesia
- Interventions
- Multimodal Anesthesia Monitoring (BIS, SPI, TOF), Standard Anesthesia Monitoring
- First posted
- 2026-10-26
- Last updated
- 2026-10-27
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of Postoperative Anesthesia-Related Complications | Within 48 hours after surgery | Proportion of participants experiencing at least one anesthesia-related postoperative complication, including delayed recovery of spontaneous breathing, postoperative nausea and vomiting (PONV), shivering, postoperative residual neuromuscular blockade (PORC), or constipation. Each participant was counted once if one or more of these complications occurred. |
| Secondary | Mean Intraoperative Remifentanil Infusion Rate | During surgery, from induction to discontinuation of anesthesia | Mean remifentanil infusion rate administered during general anesthesia, expressed in micrograms per kilogram of body weight per minute (μg/kg/min), compared between the multimodal monitoring and standard monitoring groups. |
| Secondary | Incidence of Supplemental Rocuronium Administration | During surgery, from induction to discontinuation of anesthesia | Proportion of participants requiring at least one additional bolus of rocuronium after the initial dose during general anesthesia, compared between the two study groups. |
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/NCT07895836
GET https://conductscience.org/api/trials/v1/NCT07895836/registered