Trial · NCT02101242
Regional Cerebral Oxygen Saturation Under General Anesthesia A Pilot Study
NCT02101242, Terminated, Charite University, Berlin, Germany
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Regional Cerebral Oxygen Saturation Under General Anesthesia A Pilot Study. Trials, record NCT02101242. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02101242
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Regional Cerebral Oxygen Saturation Under General Anesthesia A Pilot Study
- NCT number
- NCT02101242
- Status
- Terminated
- Enrollment
- 42 participants, actual
- Lead sponsor
- Charite University, Berlin, Germany
- Conditions
- Regional Cerebral Oxygen Saturation
- First posted
- 2014-04-02
- Last updated
- 2019-06-28
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Regional cerebral oxygen saturation (rSO2) | Duration of elective surgery (an average of 2 hours) | Regional cerebral oxygen saturation (rSO2) is measured under different body positions for elective surgery |
| Secondary | Incidence and severity of postoperative delirium | In the 10 - day postoperative sample period | Nursing Delirium Screening Scale (Nu-DESC), Confusion Assessment Method (CAM-ICU), Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-V) (DSM-V), International Classification of Diseases (ICD)-10 (ICD-10) |
| Secondary | Incidence and severity of postoperative cognitive dysfunction | In the 10-day postoperative sample period | Test battery: Verbal Learning Test, Stroop Colour Word Test, Letter Digit Substitution Test, Concept Shifting Test |
| Secondary | Rate of organ complications | In the 10-day postoperative sample period | |
| Secondary | Electrical activity of the brain | Duration of elective surgery (an average of 2 hours) | Electrical activity of the brain is measured by electroencephalogram (EEG-derived) bispectral index (BIS) monitoring |
| Secondary | Somatic cerebral oxygen saturation (sSO2) | Duration of elective surgery (an average of 2 hours) | Somatic cerebral oxygen saturation (rSO2) of the lower limbs (absolutely and in side comparison) in cardiac surgery patients |
| Secondary | Hospital length of stay | participants will be followed for the duration of hospital stay, an expected average of 4 weeks | Post-anaesthesia Discharge Scoring System (PADSS) |
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.
Tests2
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
| Verbal Learning | Secondary outcome | ConductCognition |
Source
- Release
- trials-2026-11-12-0.4.0
- Release manifest SHA-256
- 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
- Registry capture
- 2026-11-12
- Results copy, AACT
- 2026-03-23
- NIH clinical studies file
- 2026-11-13
Source ClinicalTrials.gov
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone 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/NCT02101242
GET https://conductscience.org/api/trials/v1/NCT02101242/registered