Last updated: September 21, 2023
Sponsor: Hospital Vall d'Hebron
Overall Status: Completed
Phase
4
Condition
Functional Dyspepsia
Heartburn
Non-ulcer Dyspepsia (Nud)
Treatment
Iberogast® and Iberogast® N
Clinical Study ID
NCT04656730
IBO
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Subject has read and signed the institutional review board-approved informed consentform before screening.
- ≥18 years old.
- Confirmed irritable bowel syndrome (ibs) or functional dyspepsia (fd) diagnosis perrome iv criteria.
- Has active symptoms of bloating.
- Subject must be willing to comply with the protocol.
- Female subjects who are capable of conceiving must use an acceptable form ofcontraception in order to participate in the study*. *women of childbearing potentialmust have a negative pregnancy test prior to randomization into the study andcommitment to use at least one of these birth control methods: male or female condomwith or without spermicide, cap, hormonal contraception, diaphragm or sponge with orwithout spermicide, intrauterine device, bilateral tubal occlusion, vasectomizedpartner, sexual abstinence during the study. based on ich, m3 (r2) 2009 a woman isconsidered of childbearing potential: fertile, following menarche and until becomingpost-menopausal unless permanently sterile. permanent sterilization methods includetubal ligation, hysterectomy, bilateral oophorectomy.
Exclusion
Exclusion Criteria:
- Presence of any organic gastrointestinal diseases.
- Subjects with known hypersensitivity to Iberogast or one of the active substances orexcipients.
- One or more medical condition(s), including renal, hepatic, hematologic,endocrinological, neurologic, or immune disease that in the opinion of theInvestigator would make the subject an inappropriate candidate for this study.
- Subjects with impaired liver function tests
- Malignant disease not in remission.
- Presence of any active infectious disease.
- Subjects not willing to stop medications that may interfere with gastrointestinalmotility during 48 h previous to the gas infusion tests. These include: bulkingagents, laxatives, linaclotide, prokinetics, antidiarrheal or opioids.
- Known alcohol or drug abuse.
- Female participants of childbearing potential with a positive pregnancy test, breastfeeding, or female participants of childbearing potential without adequatecontraception.
- Subject judged by the investigator or study staff to be unable or unlikely to complywith daily protocol requirements, or study visits.
Study Design
Total Participants: 68
Treatment Group(s): 1
Primary Treatment: Iberogast® and Iberogast® N
Phase: 4
Study Start date:
September 03, 2020
Estimated Completion Date:
January 31, 2023
Study Description
Connect with a study center
Germans Trias i Pujol Hospital
Badalona, Barcelona 08916
SpainSite Not Available
Hospital Universitari Vall d'Hebron
Barcelona, 08035
SpainSite Not Available
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