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Clinical efficacy evaluation of Tiaoganlipi prescription in treating Gastroesophageal reflux disease related Laryngologic reflux disease

Clinical efficacy evaluation of Tiaoganlipi prescription in treating Gastroesophageal reflux disease related Laryngologic reflux disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019428
Enrollment
Unknown
Registered
2018-11-10
Start date
2018-12-01
Completion date
Unknown
Last updated
2018-11-19

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

Conditions

Gastroesophageal reflux disease related Laryngologic reflux disease

Interventions

Group 1:Omeprazole Enteric-coated Tablets+Tiaoganlipi prescription granules
Group 2:Omeprazole Enteric-coated Tablets+Tiaoganlipi prescription granules analogue

Sponsors

Beijing Hospital of TCM Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. meet the GERD diagnostic standard for Laryngology and reflux disease. RSI>13 and/or RFS>7?, 24 hours, throat acid reflux event was more than 3 times or throat throat pH <4 total time was more than 1%. 2. Aged 18 to 65 years old male and female; 3. Informed consent, volunteers.

Exclusion criteria

Exclusion criteria: (1) operation history of stomach, esophagus and duodenum; (2) suffering from Zhuo AI syndrome and primary esophageal motility disease; (3) suspected or confirmed malignant diseases or any early warning symptoms; (4) PPI or H2 receptor blockers were used in the first 1 weeks; (5) severe primary heart, liver, lung, kidney, pancreas, liver, or severe diseases affecting their survival; (6) Persons with disabilities prescribed by law (blind, deaf, dumb, mental retardation, mental retardation, physical disability); (7) there is a history of alcohol or drug abuse; (8) Allergic constitution, such as those who have a history of allergy to two or more drugs or foods, or are known to be allergic to the ingredients of this drug; (9) poor compliance or failure to cooperate; (10) pregnant, pregnant or lactating.

Design outcomes

Primary

MeasureTime frame
refiux symptom index;reflux finding score;

Secondary

MeasureTime frame
TCM syndrome score;24 hour esophageal PH monitoring index;

Countries

China

Contacts

Public ContactLin Tao

Beijing Hospital of TCM Affiliated to Capital Medical University

taolin8900@163.com+86 15117908900

Outcome results

None listed

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