To know benefits of WhatsApp based platform in post PCI patients via online nursing till 1 month.
- Conditions
- Health Condition 1: I749- Embolism and thrombosis of unspecified artery
- Registration Number
- CTRI/2022/09/045935
- Lead Sponsor
- Terumo India Private Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
1.Patients who him/herself or the immediate caregiver has WhatsApp on smartphone.
2.Patients who him/herself or the immediate caregiver has self-declared comfort in reading and understanding English language.
3.Patients who have undergone Percutaneous Coronary Intervention (PCI).
4.Patients in whom stent was implanted during the PCI Procedure.
5.Patients who can be discharged from the hospital within 72 hours of PCI as per the medical judgement of the Investigator post PCI.
6.Patient or caregiver with physical and mental ability to comply with daily assessment using WhatsApp based chat Platform with remote nursing.
7.Patient or Legally acceptable representative of patient willing to sign an Informed Consent Form indicating that they understand the purpose of and the procedures required for the trial and are willing to participate in the registry. The form can be signed physically, or there can be implied (digital) consent based on WhatsApp chat initiation by the patient.
1.Patients more than 75 years of age
2.Patients who had PCI for a complex lesion that necessitated multiple stents hospitalization beyond 72 hours.
3.Patients who are being readmitted to hospital after a prior PCI will be discontinued from the assessment
4.Presence of any other clinically significant disease or laboratory findings that in the Investigatorâ??s opinion may affect the study outcomes.
5.Participation in another study concurrently or within 4 weeks prior to the Screening Visit that also has digital intervention or patient satisfaction based survey
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method