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Not yet recruiting NCT06890455

Fecal Calprotectin in Patients Infected with Intestinal Protozoan Infections

Observational Fecal Calprotectin in Intestinal Protozoa

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Fecal Calprotectin in Intestinal Protozoa. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Calprotectin extracted from stool can be detected easily using ELISA. Numerous studies have shown that fecal calprotectin concentrations demonstrate a good correlation with intestinal inflammation This study aims to detect the relationship between fecal calprotectin and Blastocystis hominis and Entamoeba histolytica infections.

Primary outcome measures

  • Prevalence of Blastocystis and Entamoeba [Time frame: 2 months]
Secondary outcome measures (1)
  • Number of persons have high fecal calprotectin [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

120 fecal samples will be collected as the following:

  • 40 samples from patients complaining of gastrointestinal manifestations and only infected with B.hominis and E.histolytica.
  • 40 samples from patients complaining of gastrointestinal manifestations without any protozoal infection.
  • 40 healthy control cross-matched volunteers (without gastrointestinal manifestations, or intestinal parasites).

Exclusion criteria

  • persons received antiparasitic drugs or antibiotic 2 weeks before sample collection Patients with mixed intestinal protozoa Patients with intestinal protozoa rather than Entamoeba histolytica and Blastocystis

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

Egypt · 1 center
  • Sohag University — Sohag

Identifiers

NCT: NCT06890455 · Soh-Med--25-3-07MS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗