Recurrence of H Pylori : Incidence and Influential Factors.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorSohag University

About this trial

This study aims to determine recurrence rates, identify influential factors, investigate key factors that contribute to recurrence, evaluate treatment effectiveness and to assess the efficacy of different eradication regimens and their role in reducing recurrence.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age: 18-75 years old.

H. pylori infection: Confirmed by endoscopy, biopsy, or non-invasive tests (e.g., urea breath test, stool antigen test).

Symptoms: Presence of dyspepsia, peptic ulcer disease, or other H. pylori-related symptoms.

Laboratory tests: Normal liver and kidney function, and no significant abnormalities in blood counts.

Disqualifiers

Patients receiving eradication therapy in the past taking proton pump inhibitors,, H2 blockers ,,bismuth ,, antibiotics or other medications that interfere with the result of the examination in the recent 4 weeks.

Gastrointestinal disorders: Severe gastrointestinal disorders (e.g., gastric cancer, inflammatory bowel disease ,gastric or duodenal ulcer with current or recent bleeding , or clinical significant gastrointestinal bleeding within 4 weeks of randomization).

Malignancies: Active or recent malignancies.

Severe comorbidities: Unstable or severe comorbidities (e.g., heart failure, liver cirrhosis).

Trial design

Design model

Single group

Treatments tested in this trial

  • follow up of patients that had H. Pylori infection and recieved medical treatment for recurrence

    Behavioral

    follow up of patients that had H. Pylori infection and recieved medical treatment for recurrence and influential factors for recurrence

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: follow up of patients that had H. Pylori infection and recieved medical treatment for recurrenceOther 1 intervention

Trial outcomes

Primary outcomes

1

recurrence of H. Pylori infection in patients who recieved medical treatment

H. Pylori antigen in stool

Time frame
4 weeks after successful medical treatment

Secondary outcomes

Other outcomes

Sponsors and contacts

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