Skip to content

Comparing the number of days and device utility between two intravenous canula in patients undergoing surgery

Efficacy of long peripheral catheter (LPC) versus peripheral intravenous cannula (PIVC) for perioperative vascular access in high risk surgical patients - a randomised comparative trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/074562
Enrollment
200
Registered
2024-10-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: LONG PERIPHERAL CATHETER PLACEMENT: Patients allocated to Group LPC will be shifted to the procedure room in the operating theatre complex. The appropriate vein basilic or brachial will

Sponsors

Mahatma Gandhi Medical College and Research Institute , Pondicherry
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients above 18 years of age with need for vascular access for more than one week for perioperative indications

Exclusion criteria

Exclusion criteria: Patients with difficult venous access , emergency surgeries , immediate requirement of central venous catheter , CKD patients , pregnant patients

Design outcomes

Primary

MeasureTime frame
To measure and compare the incidence of primary device failure for 1000 catheter daysTimepoint: catheter patency will be assessed every twenty four hours until device removal

Secondary

MeasureTime frame
To calculate the cost incurred by the patient for the VAD.Timepoint: At the time of patient discharge;To identify the number of devices utilised per patient (Ratio)Timepoint: At the time of patient discharge;To measure and compare the incidence of complications for 1000 catheter days- phlebitis/ infiltration/ leak/ and thrombosis.Timepoint: Catheter will be assessed every twenty four hours for complications until device removal;To measure and compare the median catheter dwell time (Days)Timepoint: Day of device removal;To measure the patient satisfaction regarding overall performance and comfort of the VAD.Timepoint: At the time of patient discharge

Countries

India

Contacts

Public ContactDr Sivashanmugam T

Mahatma Gandhi Medical College and Research Institute

drsiva95@gmail.com9442505567

Outcome results

None listed

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