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Trial · NCT04492813

Plasmatic Concentrations of Propofol and Remifentanil in Obese and Non Obese Patients.

NCT04492813, Not applicable, Completed, University Hospital, Clermont-Ferrand

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Plasmatic Concentrations of Propofol and Remifentanil in Obese and Non Obese Patients. Trials, record NCT04492813. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04492813

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Plasmatic Concentrations of Propofol and Remifentanil in Obese and Non Obese Patients.
NCT number
NCT04492813
Status
Completed
Phases
Not applicable
Enrollment
40 participants, actual
Lead sponsor
University Hospital, Clermont-Ferrand
Conditions
General Anesthesia, Obesity
Interventions
Pharmacokinetic of propofol and remifentanil
First posted
2020-07-30
Last updated
2021-08-25

Source ClinicalTrials.gov

Registered outcomes8

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPlasma concentration of Propofol5 minutes after the insufflation of the pneumoperitoneumPlasma concentration of Propofol at different times during the maintenance phase of general anesthesia
PrimaryPlasma concentration of Propofol5 minutes after completion of the gastric slice or ligation of the bile ductsPlasma concentration of Propofol at different times during the maintenance phase of general anesthesia
PrimaryPlasma concentration of PropofolAt time of removing surgical specimen from the abdomenPlasma concentration of Propofol at different times during the maintenance phase of general anesthesia
PrimaryPlasma concentration of PropofolAt the exsufflation of the pneumoperitoneumPlasma concentration of Propofol at different times during the maintenance phase of general anesthesia
PrimaryPlasma concentration of Remifentanil5 minutes after the insufflation of the pneumoperitoneumPlasma concentration of Remifentanil at different times during the maintenance phase of general anesthesia
PrimaryPlasma concentration of Remifentanil5 minutes after completion of the gastric slice or ligation of the bile ductsPlasma concentration of Remifentanil at different times during the maintenance phase of general anesthesia
PrimaryPlasma concentration of RemifentanilAt time of removing surgical specimen from the abdomenPlasma concentration of Remifentanil at different times during the maintenance phase of general anesthesia
PrimaryPlasma concentration of RemifentanilAt the exsufflation of the pneumoperitoneumPlasma concentration of Remifentanil at different times during the maintenance phase of general anesthesia

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT04492813

GET https://conductscience.org/api/trials/v1/NCT04492813/registered