Actively Recruiting

Age: 18Years - 75Years
FEMALE
Healthy Volunteers
NCT07196735

Bio-electrical Impedance Analysis in Patients With Functional Dyspepsia

Led by Universitair Ziekenhuis Brussel · Updated on 2025-10-03

40

Participants Needed

1

Research Sites

62 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary objective of this study is to compare the BIA parameters, including Phase Angle, Fat Free Mass and Fat Mass, between women with functional dyspepsia and healthy women. All woman will undergo a bio-electrical impedance monitoring for this.

CONDITIONS

Official Title

Bio-electrical Impedance Analysis in Patients With Functional Dyspepsia

Who Can Participate

Age: 18Years - 75Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 18 - 75 years
  • Diagnosed with functional dyspepsia according to ROME IV criteria (for FD patients)
  • Functional dyspepsia not explained by upper GI endoscopy in the past 12 months, except mild gastritis (for FD patients)
Not Eligible

You will not qualify if you...

  • Clinical suspicion of organic disorders other than functional dyspepsia
  • Abnormal upper GI endoscopy findings other than mild gastritis (for FD patients)
  • Known reflux oesophagitis Los Angeles grade C or D, Barrett oesophagus, or peptic stricture
  • Helicobacter pylori infection unless treated at least 6 months prior
  • Known inflammatory bowel disease
  • Known major intestinal motility disorder
  • Alcohol consumption exceeding 14 units per week or other substance abuse
  • Active psychiatric disorder
  • Known systemic or autoimmune disorders affecting the GI system
  • Prior abdominal surgery except cholecystectomy or appendectomy
  • Any previous cancer diagnosis except basocellular carcinoma
  • Current chemotherapy treatment
  • History of gastroenteritis within the past 12 weeks
  • Use of dietary supplements unless at a stable dose for over 12 weeks
  • Treatment with neuromodulators unless stable dose for over 12 weeks
  • Use of proton pump inhibitors in the past 8 weeks
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UZ Brussel

Brussels, Belgium, 1090

Actively Recruiting

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Research Team

S

Sebastien Kindt

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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