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A study to evaluate the ability and also to assess the risks of Intravenous line Organizer in patients admitted in speciality wards of General Hospitals.

An open labelled, randomized, controlled clinical trial to study the performance and safety of Intravenous line Organizer in patients admitted to tertiary teaching hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/049072
Enrollment
120
Registered
2023-01-18
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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

Conditions

Health Condition 1: X- New Technology

Interventions

Intervention1: Intravenous line Organizer: An intravenous line organizing system will be attached to patients forearm or wrist. to organize one or several IV lines, preventing entanglement and contami

Sponsors

Derryl Burke
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Emergency rooms for patient hydration line (Glucose), Haematology, Pediatrics up to 18 years, Operations (OR) I.C.U. (Intensive Care Units) From simple to complicated

Exclusion criteria

Exclusion criteria: 1.Skin allergy 2.Skin burns 3. Pregnant and lactating women 4. Psychiatric illness patients 5. Severe illness patients 6. Not willing to obtain informed consent

Design outcomes

Primary

MeasureTime frame
To assess the greater autonomy, mobility and comfort using a global scale (0-4 scale where 0- no mobility and 4- highest mobility) by a physician, nurse and patient or patient care giverTimepoint: Visit 1 (Baseline) Visit 2 (During the study) Visit 3 (End of the study)

Secondary

MeasureTime frame
.To assess the adverse eventsTimepoint: Start to End of study;To assess the Device Usability questionnaire on subjectâ??s perception by nurse and patient or patient care giverTimepoint: End of study;To assess the ease of operability and set up by a physician, nurse and patient or patient care giver (0- Not easy and 4- Very Easy)Timepoint: Start to end of study;To assess the Severity of Intravenous Line Entanglement by Medical Line Entanglement scale by a physician, nurse and patient or patient care giverTimepoint: Start to End of the study;To assess the skin irritationTimepoint: Start to End of study

Countries

India

Contacts

Public ContactBaburao Vikram

Sapthagiri Institute of Medical Sciences and Research

pahuli2124@gmail.com9741734968

Outcome results

None listed

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