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A prospective study of the optimal treatment plan to improve the emotional disorders in patients of gastroesophageal reflux disease

A prospective study of the optimal treatment plan to improve the emotional disorders in patients of gastroesophageal reflux disease

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002101
Enrollment
Unknown
Registered
2012-03-08
Start date
2012-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Gastroesophageal Reflux Disease (GERD)

Interventions

Combined drugs treatment group:Deanxit, take 1 pill twice a day after breakfast and lunch each
Esomeprazole, take 40mg/day before breakfast.
one drug treatment group:Esomeprazole, take 40mg/day before breakfast.

Sponsors

Institute of Surgery Research, Daping Hospital, Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Male or female, age from 18 to 65; (2) Did not accept acid suppression therapy, use any sedative-hypnotic and anti-anxiety or depression products within past 2 weeks; (3) The diagnosis of GERD (GERDQ >=8; Gastroscopy shows reflux esophagitis or Barrett's Esophagus; PH determination prompts acid reflux; meet any of the conditions above)(ference to the standards of Los Angeles, the grading of reflux esophagitis under endoscopy are as follows: Class A lesions is confined to the esophageal mucosal folds, length 0.5cm; Class C lesions in the mucous membrane fusion at the top, but does not surround the entire esophageal wall; Class D lesions fusion with each other, and the range > 75% of the esophageal wall. Diagnosis of Barrett's Esophagus: pathology prompts intestinal metaplasia.); (4) HAD emotional determination, anxiety or depression score >=8; (5) Sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) The biochemical,endoscopic and other checks suggest peptic ulcer, gastrointestinal tumors, as well as diabetes, scleroderma, neurological diseases, severe liver diseases, heart disease, malignancy, and alcoholism; (2) Women who are pregnant or in lactation; (3) Participated in other clinical trials within three months before this; (4) Difficult to complete the follow-up or various of other factors affect the compliance; (5) Persons has an allergy to drugs used in this study.

Design outcomes

Primary

MeasureTime frame
GerdQ;

Countries

China

Contacts

Public ContactLan ChunHui
tiandaochouqin99@hotmail.com+86 13896067599

Outcome results

None listed

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