Comparative Effects of Ciprofol and Propofol on Pain Intensity on the First Day After Surgery: a Retrospective, Propensity Score Matched, Cohort Study

Comparative Effects of Ciprofol and Propofol on Pain Intensity of the Patients Without PCA on the First Day After Surgery: a Retrospective, Propensity Score Matched, Cohort Study

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06020469

Enrollment

6500

Registered

2023-08-31

Start date

2023-10-31

Completion date

2023-12-31

Last updated

2023-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Pain, Anesthesia, Risk Reduction

Keywords

Data Platform, Machine Learning, Postoperative Acute Pain

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.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 80 Years

Healthy volunteers

Yes

Inclusion criteria

* Patients were included if they were above 18 years old, undergoing non-local anesthesia surgery.

Exclusion criteria

* 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.

Design outcomes

Primary

Measure	Time frame
Area under the curve	October 2022 to October 2023

Countries

China

Contacts

Primary ContactHui Zhang

zhanghui@gd2h.org.cn13719136792

Outcome results