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Clinical Trials/CTRI/2025/05/087986
CTRI/2025/05/087986Not yet recruitingNot Applicable

A randomized controlled trial to assess the effectiveness of nurse-led intervention package on transradial access site care for patients undergoing percutaneous coronary intervention on selected outcome variables admitted in cardiology units, Advanced Cardiac Centre, PGIMER, Chandigarh, 2024-26.

Damini1 site in 1 country100 target enrollmentStarted: June 16, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
vascular complications and Pain

Study Overview

Brief Summary

A randomized controlled trial to assess the effectiveness of the "nurse-ledintervention package on transradial access site care" for patientsundergoing percutaneous coronary intervention on selected outcome variables admitted incardiology units, Advanced Cardiac Centre, PGIMER, Chandigarh, 2024-26.  A total of 100 adult patients will be enrolled and randomized equally into control and experimental groups. The intervention group will receive a structured nurse-led care package focusing on education, complication prevention, pain management, activity guidelines, and follow-up care post-PCI via the transradial route, while the control group will receive routine care. Outcome variables include incidence of vascular complications (bleeding, ecchymosis, hematoma), pain level, comfort, knowledge, and hypoesthesia. The study is expected to provide evidence for the effectiveness of nurse-led interventions in improving clinical and patient-reported outcomes post-transradial PCI.

Study Design

Study Type
Interventional
Allocation
Other
Masking
Not Applicable

Eligibility Criteria

Ages
18.00 Year(s) to 99.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •1 Patients equal or more than 18 year 2 Both male and female willing to participate 3 Able to understand hindi english and punjabi language.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

vascular complications and Pain

Time Frame: At baseline, immediate+ within 24 hours+ at discharge, at two weeks after PCI.

Secondary Outcomes

  • Knowledge(Immediate)

Investigators

Sponsor
Damini
Sponsor Class
Research institution and hospital

Study Sites (1)

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