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Clinical application of PICC catheterization in children with difficult venous access

Clinical application of PICC catheterization in children with difficult venous access

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099499
Enrollment
Unknown
Registered
2025-03-25
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

difficult venous access

Interventions

T-PICC:The intervention group use tunnel PICC
PICC:The control group was treated with traditional PICC

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1 Children with difficult venous access requiring long-term intravenous infusion; 2 The presence of difficult venous access requires continuous infusion of irritating or corrosive drugs; 3 Age = 1 month; 6 Voluntary participation in this study by children or their caregivers.

Exclusion criteria

Exclusion criteria: 1 Allergic to catheter material; 2 There is a serious irremediable coagulation dysfunction; 3 The preset site has a recent history of radiotherapy and vascular surgery; 4 There is acute thrombus in the preset blood vessel; 5 Confirmed or suspected vascular-related infections, bacteremia, and sepsis.

Design outcomes

Primary

MeasureTime frame
One-time tube placement success rate;Incidence of PICC complications during catheterization;

Secondary

MeasureTime frame
One-time puncture success rate (day of catheterization);The indwelling time after tube placement;Quality of life score during catheter;Pain score (Time: day of implantation;Operation time (Time: day of tube placement);Local tissue injury: (Time: within 24h after successful catheterization);

Countries

China

Contacts

Public ContactZhang Jinghui

Xiangya Hospital, Central South University

401212@csu.edu.cn+86 158 7403 2339

Outcome results

None listed

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