Screening of Lactose Intolerance Among IBS Patients Diarrhea Dominant

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorAssiut University

About this trial

This cross-sectional study aims to determine the prevalence of lactose intolerance among patients with chronic diarrhea, assess its correlation with age and gender, and evaluate common symptoms in affected patients. The study will collect demographic data, conduct lactose intolerance testing via PCR, and use a symptom questionnaire.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Related to defecation (pain improves or worsens with bowel movements).

Change in stool frequency (diarrhea or constipation).

Change in stool form (appearance) (loose, watery, hard, or lumpy).

Patients aged >18 years.

Disqualifiers

-patient aged<18 years old.

Patients with chronic diarrhea don't meet Rome criteria

patients with malignancies

Trial population

The study population consists of adult patients aged 18-70 years diagnosed with chronic diarrhea lasting more than four weeks. Both male and female participants are included. Participants will be recruited from a single healthcare center. They will undergo comprehensive assessments, including demographic profiling, medical history review, and diagnostic testing for lactose intolerance using PCR. The diversity in age and gender ensures that potential correlations with these variables can be analyzed.

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

70 Participants
are grouped into 1 trial group
Group A: adult patients aged 18-70 years diagnosed as IBS diarrhea dominant

Trial outcomes

Primary outcomes

1

Prevalence data on lactose intolerance in patients with IBS diarrhea dominant.

The primary outcome is to determine the percentage of patients with chronic diarrhea who test positive for lactose intolerance using PCR testing.

Time frame
1 year

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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