KCT0004179
Not Yet Recruiting
N/A
The Comparative study of Voice quality improvement according to Ilaprazole administration on Laryngopharyngeal reflux disease patients with Voice change
Koera University Guro Hospital0 sites140 target enrollmentTBD
ConditionsDiseases of th respiratory system
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Diseases of th respiratory system
- Sponsor
- Koera University Guro Hospital
- Enrollment
- 140
- Status
- Not Yet Recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(1\) Those who don't lack decision\-making capacity, with the age of between 19 and 75
- •(2\) Those suffering from voice disorder with the score of Reflux Symptom index (RSI) and Reflux Finding score (RFS) higher than 13 and 7 point.
- •(3\) Those who agree to participate in this clinical trial voluntarily.
Exclusion Criteria
- •(1\) Those sensitive to class of Ilaprazole (Proton pump inhibitor)
- •(2\) Those with history of malignant tumor
- •(3\) Those with need to take Warfarin, Coumarin, Aspirin(higher then 325mg/d) or steroid consistently.
- •(4\) Those with history of surgery or treatment due to Gastroesophageal reflux disease (GERD)
- •(5\) Those with history of Gastric acid suppression
- •(6\) Those with history of significant surgery which has impact on Gastric acid secretion
- •(7\) Those taking Gastric acid suppression medicine
- •(8\) Mental illiness patient, alcohol addictor or those with history of drug abuse
- •(9\) Pregnant and lactating women
- •(10\) Childbearing women (Menopausal women who are amenorrheic for at least 12 months are considered to be non\-childbearing women.)
Outcomes
Primary Outcomes
Not specified
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