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Clinical efficacy analysis of Vonoprazan in the treatment of pharyngeal reflux disease

Clinical efficacy analysis of Vonoprazan in the treatment of pharyngeal reflux disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090530
Enrollment
Unknown
Registered
2024-10-08
Start date
2024-10-08
Completion date
Unknown
Last updated
2024-10-15

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

Conditions

laryngopharyngeal reflux disease

Interventions

Exposed group (Oral vonoprazan):none
non-exposed group (Oral rabeprazole):none

Sponsors

Yichang Central People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ?All patients had LPRD symptoms for at least 3 months, and LPRD was diagnosed based on their RSI =13 points and/or RFS =7 points; ? Age ? 18 years old, regardless of gender; ?No medication has been administered in the last 14 days; ?Can complete the questionnaire under the guidance of the doctor and cooperate with the follow-up; ?Patients gave informed consent to receive outpatient and hospitalized questionnaires and related information will be used for clinical research.

Exclusion criteria

Exclusion criteria: ? Recent acute inflammation of the pharynx (e.g., upper respiratory tract infection, acute tonsillitis, acute epiglottitis, acute laryngitis, etc.); ? Have a history of allergic rhinitis or asthma; ? Have a history of previous trauma to the throat or neck; ?History of cervical or thoracic spine disease; ? History of previous surgery on the throat, head and neck radiotherapy and acupuncture.

Design outcomes

Primary

MeasureTime frame
Overall efficiency;

Secondary

MeasureTime frame
General Information;

Countries

China

Contacts

Public Contactwenxia He

Xiling Campus of Yichang Central People's Hospital

1298091021@qq.com+86 136 5717 0417

Outcome results

None listed

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