NCT07683611

Brief Summary

This randomized study compared two ultrasound-guided techniques for placing a peripheral intravenous cannula in adults aged 20 to 60 years who required intravenous access. Participants were assigned equally to either the short-axis out-of-plane approach or the long-axis in-plane approach. The study evaluated whether the techniques differed in successful cannulation. It also compared cannulation time, number of attempts, and immediate complications, including arterial puncture, extravasation, and haematoma.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
222

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 7, 2023

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 7, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 7, 2024

Completed
2.1 years until next milestone

First Submitted

Initial submission to the registry

June 28, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 6, 2026

Completed
Last Updated

July 6, 2026

Status Verified

June 1, 2026

Enrollment Period

6 months

First QC Date

June 28, 2026

Last Update Submit

June 28, 2026

Conditions

Keywords

Ultrasound-Guided Peripheral Intravenous CannulationShort-Axis Out-of-Plane ApproachLong-Axis In-Plane ApproachPeripheral Intravenous AccessInterventional Ultrasonography

Outcome Measures

Primary Outcomes (1)

  • Successful Peripheral Intravenous Cannulation

    Cannulation was considered successful when the catheter advanced without resistance, blood returned freely into the hub, and saline could be flushed without local swelling. The outcome was recorded as successful or unsuccessful.

    Immediately following the assigned cannulation procedure

Secondary Outcomes (1)

  • Cannulation Time

    uring the assigned cannulation procedure

Study Arms (2)

Short-Axis Out-of-Plane Approach

EXPERIMENTAL

Participants underwent ultrasound-guided peripheral intravenous cannulation with the probe positioned perpendicular to the target vein to obtain a transverse image. The needle was advanced using an out-of-plane technique.

Procedure: Short-Axis Out-of-Plane Ultrasound-Guided Cannulation

Long-Axis In-Plane Approach

ACTIVE COMPARATOR

Participants underwent ultrasound-guided peripheral intravenous cannulation with the probe positioned parallel to the target vein to obtain a longitudinal image. The needle was advanced in plane while maintaining visualization of the needle tip.

Procedure: Long-Axis In-Plane Ultrasound-Guided Cannulation

Interventions

The ultrasound probe was positioned perpendicular to the target vein to obtain a transverse image. A peripheral intravenous cannula was inserted by advancing the needle using the out-of-plane technique under real-time ultrasound guidance.

Short-Axis Out-of-Plane Approach

The ultrasound probe was positioned parallel to the target vein to obtain a longitudinal image. A peripheral intravenous cannula was inserted by advancing the needle in plane while maintaining visualization of the needle tip under real-time ultrasound guidance.

Long-Axis In-Plane Approach

Eligibility Criteria

Age20 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Men and women aged 20 to 60 years
  • Required peripheral intravenous access

You may not qualify if:

  • Body mass index of 30 kg/m² or greater
  • Infection at the intended cannulation site
  • Upper-limb deformity
  • Previous venous thrombosis
  • Refusal to participate

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Medical Teaching Institution-Lady Reading Hospital

Peshawar, Khyber Pakhtunkhwa, Pakistan

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants were randomly assigned in a 1:1 ratio to one of two parallel groups. One group received ultrasound-guided peripheral intravenous cannulation using the short-axis out-of-plane approach, while the other received the long-axis in-plane approach. Each group included 111 participants.
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PGR

Study Record Dates

First Submitted

June 28, 2026

First Posted

July 6, 2026

Study Start

November 7, 2023

Primary Completion

May 7, 2024

Study Completion

May 7, 2024

Last Updated

July 6, 2026

Record last verified: 2026-06

Locations