Quality of Life Clinical Trial
Official title:
The Study of Efficacy and Adverse Effects of Prapchompoothaweep Remedy Crude Drug and Loratadine for Treatment in Allergic Rhinitis Patients (Clinical Trials Phase II)
1. To compare the effectiveness of Prapchompoothaweep crude drug at 3,000 mg per day and
Loratadine 10 mg per day for treatment in Allergic Rhinitis patients. (Clinical Trial
Phase II)
2. To evaluate the safety and adverse effect of Prapchompoothaweep crude drug at 3,000 mg
and Loratadine 10 mg for Allergic Rhinitis patients.
this study is a double blind randomized controlled trial study.
the volunteers will be divided into 2 groups. One is received Prapchompoothaweep crude drug
capsule at 1,000 mg 3 times a day before meals and the other is received Loratadine 10 mg per
day before meals. it takes 6 weeks to complete the project for each volunteers.
Before enrolling, volunteers will stop using any anti-histamine drug for 1 week (wash-out
period). All volunteers will be followed up in the 3rd and 6th week to evaluate the efficacy
and adverse effect after received drugs.
The researcher will record characteristic data such as gender, age, BMI, vital signs and
symptoms . The adverse effect will be monitored by hematology test e.g. liver function test,
renal function test, lipid profile and blood sugar test.
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