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Analysis of factors related to postoperative vomiting in interventional therapy: a single-center retrospective case-control study

Analysis of factors related to postoperative vomiting in interventional therapy: a single-center retrospective case-control study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092672
Enrollment
Unknown
Registered
2024-11-21
Start date
2024-11-30
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Nausea, vomiting

Interventions

Case group (vomiting occurred):postoperative nausea and vomiting, PONV
Control group (vomiting did not occur):postoperative nausea and vomiting, PONV

Sponsors

The First Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients undergoing interventional therapy in vascular surgery from January 1, 2020 to December 31, 2023; 2.Age > 18 years old; 3.Local anesthesia or monitoring anesthesia;

Exclusion criteria

Exclusion criteria: 1.Preoperative concurrent or acute or chronic digestive tract disease or nausea, vomiting, acid reflux, belching from any cause; 2.General anesthesia or general anesthesia within 1 month; 3.chemotherapy;

Design outcomes

Primary

MeasureTime frame
Contrast agent dosage;—

Secondary

MeasureTime frame
weight;Glomerular filtration rate;—

Countries

China

Contacts

Public ContactChunFang Hu

The First Affiliated Hospital of Army Medical University

2123996523@qq.com+86 23 6876 5755

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026