Trial · NCT07568938
Evaluation of the Stress Response in Anesthesia Use Inhalation Anesthetic (Desflurane) Versus TIVA for Bariatric Surgery
NCT07568938, Not applicable, Recruiting, G.Gennimatas General Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Evaluation of the Stress Response in Anesthesia Use Inhalation Anesthetic (Desflurane) Versus TIVA for Bariatric Surgery. Trials, record NCT07568938. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07568938
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Evaluation of the Stress Response in Anesthesia Use Inhalation Anesthetic (Desflurane) Versus TIVA for Bariatric Surgery
- NCT number
- NCT07568938
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 70 participants, estimated
- Lead sponsor
- G.Gennimatas General Hospital
- Conditions
- Opioid Use, Bariatric Surgery Candidate, TCI Eleveld, Obesity
- Interventions
- opioid free anesthesia, Opiod Free Anesthesia with TCI ELEVELD
- First posted
- 2026-05-06
- Last updated
- 2026-05-06
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Perioperative trend of Cortisole | At baseline, at the end of the operation, 24 hours after surgery] | |
| Primary | Perioperative trend of Adrenaline | At baseline, at the end of the operation, 24 hours after surgery | |
| Primary | Perioperative trend of Noradrenaline | At baseline, at the end of the operation, 24 hours after surgery | |
| Primary | Perioperative trend of Dopamine | Time Frame: At baseline, at the end of the operation, 24 hours after surgery | |
| Primary | Perioperative trend of Prolactine | Time Frame: At baseline, at the end of the operation, 24 hours after surgery | |
| Primary | Perioperative trend of ACTH | Time Frame: At baseline, at the end of the operation, 24 hours after surgery | |
| Primary | Perioperative trend of Lactate | Time Frame: At baseline, at the end of the operation, 24 hours after surgery | |
| Secondary | Plasma levels of Propofol for patients receiving Propofol TCI | Immediately after extubation | |
| Secondary | Anesthesia related adverse effects reported, including intraoperative hemodynamic instability, postoperative hypoxemia, nausea and vomit | Baseline (preoperative), immediately postoperatively, and 24 hours postoperatively During surgery and through 24 hours after surgery, Immediately after extubation Up to 24 hours postoperatively, DAY 2 DAY 15 and DAY 30 postoperative (QoR-40) | |
| Secondary | Long-term and short-term quality of anesthesia recovery | Post operatively Day 1, Day 2 Day 15 and Day 30 | Evaluation through the use of questionnaires QoR 40 |
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/NCT07568938
GET https://conductscience.org/api/trials/v1/NCT07568938/registered