MedPath

Open International Study on Quality of Life in Irritable Bowel Syndrome (IBS) Patients Before and After 8 Weeks Treatment With Mebeverine/Pinaverium Bromide

Completed
Conditions
Irritable Bowel Syndrome
Registration Number
NCT01678781
Lead Sponsor
Abbott
Brief Summary

A study to evaluate, by country and overall, the changes from baseline of the irritable bowel syndrome quality of life (IBS QoL) total score after 4 and 8 weeks of treatment with Duspatalinยฎ or Dicetelยฎ in IBS patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
607
Inclusion Criteria
  • Irritable bowel syndrome patients diagnosed by Rome III criteria (18 years or older)
Exclusion Criteria
  • Pregnancy and lactation
  • Specific contraindications to mebeverine hydrochloride or pinaverium bromide

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in Irritable Bowel syndrome (IBS) quality of life (QoL) measure (IBS-QoL) to assess the impairment of QoL in IBS patientsFrom baseline up to the week 8 visit
Secondary Outcome Measures
NameTimeMethod
Change in abdominal painFrom baseline up to the week 8 visit
Change in bloatingFrom baseline up to the week 8 visit
Change in feeling of abdominal distensionFrom baseline up to the week 8 visit
Change in stool frequencyFrom baseline up to the week 8 visit
Change in stool formFrom baseline up to the week 8 visit
Change in straining of evacuationFrom baseline up to the week 8 visit
Change in urgency of evacuationFrom baseline up to the week 8 visit
Change in feeling of incomplete evacuationFrom baseline up to the week 8 visit

Trial Locations

Locations (24)

Site reference ID/Investigator# 94523

๐Ÿ‡ฒ๐Ÿ‡ฝ

Tampico, Mexico

Site reference ID/Investigaot# 94525

๐Ÿ‡ฒ๐Ÿ‡ฝ

Guadalajara, Mexico

Site Reference ID/Investigator# 85297

๐Ÿ‡ต๐Ÿ‡ฑ

Bialystok, Poland

Site Reference ID/Investigator# 85296

๐Ÿ‡ต๐Ÿ‡ฑ

Lodz, Poland

Site reference ID/Investigator# 85313

๐Ÿ‡ต๐Ÿ‡ฑ

Olsztyn, Poland

Site Reference ID/Investigator# 85294

๐Ÿ‡ต๐Ÿ‡ฑ

Poznan, Poland

Site Reference ID/Investigator# 85295

๐Ÿ‡ต๐Ÿ‡ฑ

Poznan, Poland

Site reference ID/Investigator# 94521

๐Ÿ‡จ๐Ÿ‡ณ

Guangzhou, China

Site reference ID/Investigator # 94518

๐Ÿ‡จ๐Ÿ‡ณ

Shanghai, China

Site reference ID/Investigator # 94515

๐Ÿ‡จ๐Ÿ‡ณ

Wuhan, China

Site reference ID/Investigator# 95475

๐Ÿ‡จ๐Ÿ‡ณ

Guangzhou City, China

Site reference ID/Investigator# 94519

๐Ÿ‡จ๐Ÿ‡ณ

Beijing, China

Site reference ID/Investigator# 95900

๐Ÿ‡ช๐Ÿ‡ฌ

Cairo, Egypt

Site reference ID/Investigator# 95902

๐Ÿ‡ช๐Ÿ‡ฌ

Giza, Egypt

Site reference ID/Investigator # 94516

๐Ÿ‡จ๐Ÿ‡ณ

Shanghai, China

Site Reference ID/Investigator# 95908

๐Ÿ‡ช๐Ÿ‡ฌ

Alexandria, Egypt

Site reference ID/Investigator # 94517

๐Ÿ‡จ๐Ÿ‡ณ

Shanghai, China

Site Reference ID/Investigator# 85293

๐Ÿ‡ต๐Ÿ‡ฑ

Katowice, Poland

Site reference ID/Investigator# 95901

๐Ÿ‡ช๐Ÿ‡ฌ

El Sharkya, Egypt

Site Reference ID/Investigator# 85298

๐Ÿ‡ต๐Ÿ‡ฑ

Bydgoszcz, Poland

Site Reference ID/Investigator# 95906

๐Ÿ‡ช๐Ÿ‡ฌ

Port Said, Egypt

Site refernce ID/Investigator# 94527

๐Ÿ‡ฒ๐Ÿ‡ฝ

Mexico City, Mexico

Site reference ID/Investigator# 85314

๐Ÿ‡ต๐Ÿ‡ฑ

Bialystok, Poland

Site reference ID/Investigator# 95903

๐Ÿ‡ช๐Ÿ‡ฌ

Giza, Egypt

ยฉ Copyright 2025. All Rights Reserved by MedPath