Effect of Cerebral Oxygen Saturation Monitoring on POCD of Elderly Patients Undergoing Shoulder Arthroscopy
NCT05615480, Not applicable, Unknown, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Effect of Cerebral Oxygen Saturation Monitoring on POCD of Elderly Patients Undergoing Shoulder Arthroscopy | ClinicalTrials.gov |
| NCT number | NCT05615480 | ClinicalTrials.gov |
| Status | Unknown | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 400 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University | ClinicalTrials.gov |
| Conditions | Cerebral Oxygen Saturation, Postoperative Cognitive Function | ClinicalTrials.gov |
| Interventions | Controlled hypotension guided by cerebral oxygen saturation monitoring | ClinicalTrials.gov |
| First posted | 2022-11-14 | ClinicalTrials.gov |
| Last updated | 2023-04-13 | ClinicalTrials.gov |
Registered outcomes 8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Incidence of postoperative cognitive dysfunction(POCD) 3 days after operation | 3 days after operation | The Neuropsychological test, includes: (1) Vocabulary learning; (2) Vocabulary recall; (3) Connection test; (4) Stroop Color word interference; (5) Letter-number coding test. | ClinicalTrials.gov |
| Secondary | Incidence of postoperative cognitive dysfunction(POCD) 14 days after operation | 14 days after operation | The Neuropsychological test, includes: (1) Vocabulary learning; (2) Vocabulary recall; (3) Connection test; (4) Stroop Color word interference; (5) Letter-number coding test. | ClinicalTrials.gov |
| Secondary | Incidence of postoperative cognitive dysfunction(POCD) 3 months after operation | 3 months after operation | The Neuropsychological test, includes: (1) Vocabulary learning; (2) Vocabulary recall; (3) Connection test; (4) Stroop Color word interference; (5) Letter-number coding test. | ClinicalTrials.gov |
| Secondary | Expression changes of cognitive function related markers 24 hours after operation | 24 hours after operation | Patients consented on blood sampling receive marker analysis from blood（S100β、NSE and IL-6). | ClinicalTrials.gov |
| Secondary | Hospital stay | through hospitalization period, an average of 15 day | Hospital stay | ClinicalTrials.gov |
| Secondary | Hospital expenses | through hospitalization period, an average of 15 day | Hospital expenses | ClinicalTrials.gov |
| Secondary | Perioperative complications | 1 day (during the surgical period) | Complications during the surgical period | ClinicalTrials.gov |
| Other | Safety outcomes | through study completion, an average of 1 year | Complications and adverse reactions of patients during the study period | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 14
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|---|---|
| 9525362 | BACKGROUND | PubMed |
| 11739990 | BACKGROUND | PubMed |
| 19225398 | BACKGROUND | PubMed |
| 20626359 | BACKGROUND | PubMed |
| 20650659 | BACKGROUND | PubMed |
| 22068873 | BACKGROUND | PubMed |
| 22311364 | BACKGROUND | PubMed |
| 23415820 | BACKGROUND | PubMed |
| 26358703 | BACKGROUND | PubMed |
| 27127919 | BACKGROUND | PubMed |
| 27285000 | BACKGROUND | PubMed |
| 29161395 | BACKGROUND | PubMed |
| 29396097 | BACKGROUND | PubMed |
| 31166241 | BACKGROUND | PubMed |
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 1
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 | Primary outcome | ConductCognition |
Source 4
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.3.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 4a570df2e7274cee2d4fa2959402fab41880e2cd412e4b590390035fbea69391 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
Release trials-2026-11-12-0.3.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.