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An Exploratory Study of Perioperative Venous Access in Obese Patients

An Exploratory Study of Perioperative Venous Access in Obese Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06031545
Enrollment
528
Registered
2023-09-11
Start date
2023-12-01
Completion date
2025-12-30
Last updated
2023-09-11

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

Conditions

Catheter Complications

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.

Interventions

OTHERLong peripheral venous catheters for use

Long peripheral venous catheters for use during the perioperative period in obese patients

OTHERMidline catheter

Midline catheters for use during the perioperative period in obese patients

Sponsors

Sir Run Run Shaw Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Masking description

Not possible because of the material and characteristics of the catheter

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Catheter-related complication rateduring catheter indwelling,an average of 2 weeksThe proportion of patients with complications as a proportion of the total number of cases

Secondary

MeasureTime frameDescription
Catheter retention daysduring catheter indwelling,an average of 2 weeksNumber of days from the day of catheter placement to the day of extubation
Completion rate of treatment via one catheterduring catheter indwelling,an average of 2 weeksNumber of patient cases in which all infusion treatments were completed via one catheter/total number of patient cases

Countries

China

Contacts

Primary ContactLinfang Zhao
3193159@zju.edu.cn+86 13588819123
Backup ContactXiuzhu Cao
Caoxz@srrsh.com+86 13588477316

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026