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Local Effect of sheep ghee on complication after Angiography

Investigation of the Local Effect of bovine ghee on complication after Angiography in Patients Under Coronary Angiography Admitted to Ali-ibn Abitaleb Hospital in Rafsanjan City in 2018-2019

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180729040630N2
Enrollment
135
Registered
2019-03-11
Start date
2018-08-23
Completion date
Unknown
Last updated
2019-03-25

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

Conditions

Complications after Angiography. Bleeding

Interventions

Intervention 1: Intervention group: Cow oil. Intervention 2: Intervention group: Sheep oil. Intervention 3: Control group: Vaseline cream.

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients undergoing coronary angioplasty Performing angiography via femoral artery Lack of heart failure Lack of COPD Lack of kidney failure Lack of severe valve disease Lack of liver failure Lack of Blood disorders Using Sheath 6 to access the artery pathway Not having known psychiatric disorders Fluency in Farsi and ability to communicate Systolic blood pressure is less than 130 Lack of ecchymosis in the angiography site Lack of hematoma in the angiography site Lack of hemorrhage in the angiography site Not taking steroids, heparin and enoxaparin Age more than 18 years old

Exclusion criteria

Exclusion criteria: Drug side effects History of localized allergy to animal oil The incidence of non-vascular complications of Angiography in the patient Types of cardiac dysrhythmia Contrast agents Cardiac tamponed Cerebrovascular accident (CVA) Pulmonary edema Cardio-respiratory arrest Decreased consciousness Angioplasty Emergency Surgery Lack of cooperation Personal satisfaction and discharge

Design outcomes

Primary

MeasureTime frame
Complication after Angiography. Timepoint: Before and after intervention. Method of measurement: Christenson's guideline, Visual Satisfaction Scale of Patients, Visual Scale of Pain And Fatigue Assay Scale for Routine Patients.

Secondary

MeasureTime frame
Satisfaction of Patients. Timepoint: Before and after intervention. Method of measurement: Visual Satisfaction Scale of Patients.;Pain. Timepoint: Before and after intervention. Method of measurement: Visual analogue pain scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Ali Zakeri

Rafsanjan University of Medical Sciences

mazakeri@rums.ac.ir+98 34 3428 0011

Outcome results

None listed

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