Comparison effect of Lavender and Acetaminophen on Nitroglycerin-induced headache

Phase 3

Recruiting

• Conditions: Angina.; Ischaemic heart diseases; I20-I25

• Registration Number: IRCT20180927041157N1
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 14 January 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

Receiving Nitroglycerin infusion for the first time
Receiving Acetaminophen PRN
Not having a history of sublingual Nitroglycerin use
Not having a history of migraine or chronic headaches
No sensitivity to Acetaminophen
No sensitivity to medicinal Plants
Lack of olfactory disorders
Ability to swallow
Ability to speak

Exclusion Criteria

Hypotension
Drug susceptibility

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain scale by VAS scale. Timepoint: The evaluation of the patient's headache at 5, 10, 15, and 60 minutes after the onset of Nitroglycerine infusion. Method of measurement: The evaluation of the patient's headache in three groups (Acetaminophen, Lavender essential oil and control) at 5, 10, 15, and 60 minutes after the onset of Nitroglycerine infusion will be measured.;Comfort scale by VAS scale. Timepoint: The evaluation of the patient's comfort 15 minutes before infusion and at 60 minutes after initiation of nitroglycerin infusion. Method of measurement: The evaluation of the patient's comfort (VAS) 15 minutes before infusion and at 60 minutes after initiation of nitroglycerin infusion in three groups (acetaminophen, lavender essential oil and control) will be measured.