KCT0004179Not yet recruiting未知
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 enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 140
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional Study
Eligibility Criteria
- Ages
- 19(Year) to 75(Year) (—)
- Sex
- All
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.)
- •(11) Those who participated in other clinical trial within 30 days before screening
- •(12) Those who specialize in voice
- •(13) Those with other observed laryngopharynx disease except laryngopharyngeal reflux disease
- •(14) Those who are judged to be improper for this clinical trial
Investigators
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