Coronary angiography. Coronavirus as the cause of diseases classified elsewhere
Conditions
Interventions
Intervention 1: Intervention group: Intervention group 1 (PC6 point massage): In addition to standard postoperative care, patients in the intervention group will undergo acupressure at the PC6 point.
the difference is that pressure is applied to a non-therapeutic point with no energy meridian path, approximately 1 to 1.5 centimeters away from the actual PC6 point. Intervention 4: Pseudo Group 2 (r
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: Diagnostic angiography via femoral or radial artery and admission to CCU Age 18 to 85 years No skin lesions, ulcers, or active inflammation in the areas of the targeted pressure points (PC6 and ST36) Stable hemodynamic status based on initial assessment by the attending physician No use of medications that affect the autonomic nervous system or cardiovascular responses (such as beta-blockers, sedatives, or centrally acting antidepressants) No history of using acupressure or other similar complementary methods in the past 3 months
Exclusion criteria
Exclusion criteria: Occurrence of hemodynamic instability or need for emergency measures during the study (including need for vasopressors or cardiopulmonary resuscitation or shock) The occurrence of any acute complications after angiography (such as severe bleeding, significant arrhythmia, extensive hematoma, or embolism) Lack of effective cooperation or patient withdrawal from continuing to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean arterial pressure (MAP). Timepoint: Before intervention (Baseline), immediately after intervention, 10 minutes after intervention, 20 minutes after intervention, 30 minutes after intervention. Method of measurement: Using a digital blood pressure monitor.;Heart rate (HR). Timepoint: Before intervention (Baseline), immediately after intervention, 10 minutes after intervention, 20 minutes after intervention, 30 minutes after intervention. Method of measurement: Using a cardiac monitoring device.;Peripheral perfusion index (PI). Timepoint: Before intervention (Baseline), immediately after intervention, 10 minutes after intervention, 20 minutes after intervention, 30 minutes after intervention. Method of measurement: Using a digital pulse oximeter. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactkeyhan jafari
Hamedan University of Medical Sciences
Outcome results
None listed