Comparative Effects of Ciprofol and Propofol on Pain Intensity on the First Day After Surgery: a Retrospective, Propensity Score Matched, Cohort Study
1 other identifier
observational
6,500
1 country
1
Brief Summary
Data intelligence platform was widely used to facilitate the process of clinical research. However, a platform that integrates natural language processing (NLP) and machine learning (ML) algorithms has not been reported in perioperative medical management.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2023
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 28, 2023
CompletedFirst Posted
Study publicly available on registry
August 31, 2023
CompletedStudy Start
First participant enrolled
October 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2023
CompletedAugust 31, 2023
August 1, 2023
Same day
August 28, 2023
August 28, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Area under the curve
October 2022 to October 2023
Study Arms (2)
Numeric Rating Scale (NRS) score after surgery <4
Numeric Rating Scale (NRS) score after surgery ≥ 4
Eligibility Criteria
Pain assessment was used by Numeric Rating Scale (NRS) score after surgery.
You may qualify if:
- Patients were included if they were above 18 years old, undergoing non-local anesthesia surgery.
You may not qualify if:
- The basic information such gender, age, height, weight, and body mass index (BMI) were missing.
- Patients undergoing day surgery, with a history of multiple operations, or entering ICU after surgery, and losing the NRS score during movement at 24h after surgery.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Guangdong Second Provincial General Hospital
Guangzhou, Guangdong, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- associate chief physician
Study Record Dates
First Submitted
August 28, 2023
First Posted
August 31, 2023
Study Start
October 1, 2023
Primary Completion
October 1, 2023
Study Completion
December 1, 2023
Last Updated
August 31, 2023
Record last verified: 2023-08