Trial · NCT07895407
Effects of Ciprofol on Perioperative Neurocognitive Function in Elderly Patients Undergoing Daytime Surgery
NCT07895407, Phase 4, Enrolling by invitation, Second Affiliated Hospital of Wenzhou Medical University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effects of Ciprofol on Perioperative Neurocognitive Function in Elderly Patients Undergoing Daytime Surgery. Trials, record NCT07895407. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07895407
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects of Ciprofol on Perioperative Neurocognitive Function in Elderly Patients Undergoing Daytime Surgery
- NCT number
- NCT07895407
- Status
- Enrolling by invitation
- Phases
- Phase 4
- Enrollment
- 148 participants, estimated
- Lead sponsor
- Second Affiliated Hospital of Wenzhou Medical University
- Conditions
- PND, POCD - Postoperative Cognitive Dysfunction
- Interventions
- Ciprofol, propofol
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The incidence rate of PND | At least 1 day before the operation, 4 hours after the operation, and 24 hours after the operation. | The primary outcome was the incidence of PND within 24 hours after surgery. |
| Secondary | The DST score | At least 1 day before the operation, 4 hours after the operation, and 24 hours after the operation. | The changes in DST scores before and after the surgery |
| Secondary | The MMSE score | At least 1 day before the operation, 4 hours after the operation, and 24 hours after the operation. | The changes in MMSE scores before and after the surgery |
| Secondary | anesthetic dosage | during operation | |
| Secondary | The TMT-A/B score | At least 1 day before the operation, 4 hours after the operation, and 24 hours after the operation. | |
| Secondary | The BNT score | At least 1 day before the operation, 4 hours after the operation, and 24 hours after the operation. | |
| Secondary | The AVLT-H score | At least 1 day before the operation, 4 hours after the operation, and 24 hours after the operation. | |
| Secondary | the clock drawing test score | At least 1 day before the operation, 4 hours after the operation, and 24 hours after the operation. | |
| Secondary | The QoR-15 score | At least 1 day before the operation, 4 hours after the operation, and 24 hours after the operation. |
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 |
|---|---|---|
| Clock Drawing Task | Secondary outcome | ConductCognition |
| Trail Making Test A | Secondary outcome | ConductCognition |
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/NCT07895407
GET https://conductscience.org/api/trials/v1/NCT07895407/registered