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Effect of pinaverium on diarrhea-predominant irritable bowel syndrome overlapping functional dyspepsia

Effect of pinaverium on diarrhea-predominant irritable bowel syndrome overlapping functional dyspepsia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013684
Enrollment
Unknown
Registered
2017-12-04
Start date
2017-07-13
Completion date
Unknown
Last updated
2017-12-11

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

Conditions

irritable bowel syndrome and functional dyspepsia

Interventions

experimental group:pinaverium
control group:pinaverium and pantoprazole

Sponsors

Wuhan Union Hospital of Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Sign the informed consent form; 2. Aged between 18 and 65 years and the sex is not limited; 3. In accordance with irritable bowel syndrome diagnostic criteria of the Roman III and IV, patients are diagnosised diarrhea-predominant irritable bowel syndrome; 4. Meet the diagnosis of functional dyspepsia in Rome III criteria; 5. The upper abdominal ultrasound, esophagogastroscopy and colonoscopy were performed in the past year in a tertiary A hospital to exclude the organic and metabolic diseases; 6. The electrocardiogram was conducted in the center during the past month and the QT phase was within the normal range.

Exclusion criteria

Exclusion criteria: 1. A history of abdominal operation; 2. Concomitant medication acting on or influencing the gastrointestinal system (such as proton-pump inhibitors, H2 blockers, cholagogues, prokinetic agents, NSAIDs, theophylline) in past 5 days; 3. Combined with other gastrointestinal functional diseases(functional diarrhea, gastroesophageal reflux disease etc.); 4. Combined with other diseases such as heart, brain, liver, renal, hematopoietic, metabolic and systemic diseases(thyroid diseases, systemic sclerosis, systemic lupus erythematosus etc.), or other serious diseases affecting the survival of the patients; 5. The level of ALT, AST or total bilirubin were exceeded 1.5 times than the normal limit; 6. Combined with severe psychological disorders requiring medication; 7. Pregnant, breastfeeding or plan to pregnant; 8. Allergic to pinaverium or pantoprazole; 9. Taken apart in other clinical study within 3 month.

Design outcomes

Primary

MeasureTime frame
IBS-SSS;FD-SSS;Bristol stool type and frequency;

Secondary

MeasureTime frame
single symptom of IBS;single symptom of FD;

Countries

China

Contacts

Public ContactJinsong Liu

Wuhan Union Hospital of Huazhong University of Science and Technology

jsliu@126.com+86 13871593366

Outcome results

None listed

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