Functional Dyspepsia: Validation of a Questionnaire for Symptom Assessment in FD PDS Subgroup

Functional Dyspepsia Clinical Trial

Official title:

Validation of a Questionnaire for Symptom Assessment in Postprandial Distress Syndrome (Functional Dyspepsia)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04647955
• Other study ID #: LPDSItopride
• Status: Completed
• Phase: Phase 4
• Start date: February 22, 2013
• Est. completion date: October 2015

Study information

• Verified date: November 2020
• Source: Universitaire Ziekenhuizen Leuven
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Fuctional dyspepsia is defined as the presence of symptoms thought to originate from the gastroduodenum, in the absence of any structural or metabolic disease that is likely to explain these symptoms. To facilitate its diagnostic and therapeutic approach, the Rome consensus proposed to distinguish 2 subgroups: postprandial distress syndrome (PDS), is characterized by meal-related symptoms such as early satiation and postprandial fullness. At present, no validated instrument is available for the assessment of the symptom responsiveness in patients suffering from PDS. To develop a new PRO questionnaire, we have previously conducted focus group sessions and cognitive interviews in PDS patients to identify all relevant symptom items that characterize PDS. In this study we aim to validate the provisional Leuven Postprandial Distress Scale (LPDS) through the assessment of its consistency, reliability and ability to detect change in the framework of a controlled treatment trial.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 100
• Est. completion date: October 2015
• Est. primary completion date: October 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with PDS diagnosis as per Rome III by Rome III questionnaire (see appendix 1B)
• Patients must provide witnessed written informed consent prior to any study procedures being performed
• Patients aged between 18 and 70 years inclusive
• Male or female patients
• Patients who are capable to understand the study and the questionnaires, and to comply with the study requirements

Exclusion Criteria:

• Patients with any condition which, in the opinion of the investigator, makes the patient unsuitable for entry into the study
• Patients with an active major psychiatric condition (depression, anxiety disorder, alcohol or substance abuse). Patients who are taking a stable dose of a single antidepressant (with the exception of amitryptiline) during the last 3 months are eligible.
• Females who are pregnant or lactating.
• Patients who are H. Pylori positive or patients who received treatment for HP eradication during the last 3 months.
• Patients suffering from diabetes type 1 or type 2.
• Patients taking medication for functional dyspepsia will need a wash-out period of 2 weeks before they can be screened
• Patients with known hypersensitivity to gastroprokinetic drugs.
• Patients with confirmed gastro-intestinal disease.
• Patients with former digestive surgery affecting upper gut motility.
• Patients affected by concomitant disease responsible for digestive symptoms
• Patients presenting with predominant symptoms of irritable bowel syndrome (IBS)
• Patients presenting symptoms of EPS several times a week according to Rome III questionnaire
• Patients presenting daily symptoms of CIN on Rome III questionnaire
• Patients presenting vomiting more than one day a month.
• Patients presenting daily symptoms of Excessive belching according to Rome III questionnaire
• Patients presenting predominant GERD according to GERD questionnaire

Related Conditions & MeSH terms

• Dyspepsia
• Functional Dyspepsia
• Postprandial Fullness Syndrome
• Syndrome

Intervention

Drug:
• Itopride
Itopride is a D2 antagonist and cholinesterase inhibitor with prokinetic effects on gastric motility used to treat functional dyspepsia. Patients were treated for 8 weeks.
• Placebo
Patients were treated for 8 weeks.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Universitaire Ziekenhuizen Leuven

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Validation of LPDS questionnaire	Responsiveness of LPDS	8 weeks
Secondary	Percentage of subject that improved after treatment with itopride based on the LPDS validated questionnaire	Percentage of subjects that show a decrease of at least 0.5 in the LPDS score at the end of the treatment. We calculated the number of patients that reached the LPDS MCID (=0.5) and at a higher response threshold (=0.7) and differences between proportions were analysed with the Chi-squared test.	8 weeks
Secondary	Efficacy of itopride compared to baseline based on the LPDS validated questionnaire	Improvement of dyspepsia symptoms at the end of the treatment compared to baseline. Within each treatment arm, the change from baseline to week 8 of treatment in quantitative measures was evaluated by mixed models.	8 weeks
Secondary	Efficacy of itopride compared to baseline in the dyspepsia subgroups on based on the LPDS validated questionnaire	Improvement of dyspepsia symptoms at the end of the treatment compared to baseline. Within each treatment arm, the change from baseline to week 8 of treatment in quantitative measures was evaluated by mixed models.	8 weeks