Trial · NCT07877285
Immunonutrition and Neuromonitoring for Postoperative Delirium in Gynecologic Oncology
NCT07877285, Recruiting, Elazıg Fethi Sekin Sehir Hastanesi
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Immunonutrition and Neuromonitoring for Postoperative Delirium in Gynecologic Oncology. Trials, record NCT07877285. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07877285
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Immunonutrition and Neuromonitoring for Postoperative Delirium in Gynecologic Oncology
- NCT number
- NCT07877285
- Status
- Recruiting
- Enrollment
- 80 participants, estimated
- Lead sponsor
- Elazıg Fethi Sekin Sehir Hastanesi
- Conditions
- Postoperative Delirium (POD), Gynecologic Cancers, Malnutitrion
- Interventions
- Preoperative Immunonutritional Scoring and Intraoperative Neuromonitoring
- First posted
- 2026-10-16
- Last updated
- 2026-10-16
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of Early Postoperative Delirium | Baseline to 72 hours postoperatively | Area under the receiver operating characteristic curve (AUC-ROC) of the preoperative Controlling Nutritional Status (CONUT) score for predicting early postoperative delirium. |
| Secondary | Predictive Performance of Baseline CONUT Score for Delirium | Preoperative baseline through postoperative day 1 | Discriminative performance evaluated via Receiver Operating Characteristic (ROC) curve analysis, calculating the Area Under the Curve (AUC), sensitivity, and specificity of baseline Controlling Nutritional Status (CONUT) and Naples Prognostic scores for predicting postoperative delirium. |
| Secondary | Predictive Performance of Baseline Naples Prognostic Score for Delirium | Baseline to 72 hours postoperatively | Area under the receiver operating characteristic curve (AUC-ROC) of the preoperative Naples Prognostic Score for predicting early postoperative delirium. |
| Secondary | Cumulative Duration of Deep Anesthesia (BIS < 40) | Intraoperative period (from anesthesia induction to extubation) | Total intraoperative duration (in minutes) spent at excessive anesthetic depth, defined as Bispectral Index (BIS) values below 40. |
| Secondary | Length of Postoperative Hospital Stay | Up to 30 days postoperatively | Total duration of hospitalization (measured in days) from the date of surgery until hospital discharge. |
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/NCT07877285
GET https://conductscience.org/api/trials/v1/NCT07877285/registered