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Clinical Trials/NCT06031545
NCT06031545
Not yet recruiting
Not Applicable

An Exploratory Study of Perioperative Venous Access in Obese Patients

Sir Run Run Shaw Hospital1 site in 1 country528 target enrollmentDecember 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Catheter Complications
Sponsor
Sir Run Run Shaw Hospital
Enrollment
528
Locations
1
Primary Endpoint
Catheter-related complication rate
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

This study is intended to explore the application effect of long peripheral intravenous catheters(LPCs) and midline catheters(MCs) in the perioperative period of obese patients, aiming at providing the scientific basis for the optimal perioperative venous access for the obese patients.

Detailed Description

This study is intended to explore the application effect of long peripheral intravenous catheters(LPCs) and midline catheters(MCs) in the perioperative period of obese patients; at the same time, the LPCs will be used as the control group and the MCs as the experimental group, to compare whether the application of LPCs in the perioperative period of obese patients is not inferior to that of the MCs; the comprehensive comparison of the effect of the clinical application and the evaluation of the health economics, aiming at providing the scientific basis for the optimal perioperative venous access for the obese patients.

Registry
clinicaltrials.gov
Start Date
December 1, 2023
End Date
December 30, 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Obese patients (BMI ≥ 30kg/m2) who are to undergo surgery.
  • Expected length of hospitalisation within 2 weeks.
  • Conscious and able to communicate normally.

Exclusion Criteria

  • It is expected that perioperative medications will need to be infused via a central venous catheter (e.g. total parenteral nutrition TPN);
  • Patients with an indwelling central venous catheter on admission

Outcomes

Primary Outcomes

Catheter-related complication rate

Time Frame: during catheter indwelling,an average of 2 weeks

The proportion of patients with complications as a proportion of the total number of cases

Secondary Outcomes

  • Completion rate of treatment via one catheter(during catheter indwelling,an average of 2 weeks)
  • Catheter retention days(during catheter indwelling,an average of 2 weeks)

Study Sites (1)

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