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The Effect of Probiotic and Zinc Supplementation in Patients With Gastroesophageal Reflux Disease

The Effect of Probiotic and Zinc Supplementation in Patients With Gastroesophageal Reflux Disease

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06664008
Enrollment
120
Registered
2024-10-29
Start date
2024-11-01
Completion date
2025-10-01
Last updated
2024-10-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastro-oesophageal Reflux Disease

Brief summary

Introduction: Gastroesophageal reflux disease (GERD) is a common digestive disorder affecting the esophagus and gastro-duodenum, presenting symptoms such as acid reflux and heartburn. GERD's incidence, symptoms, and prognosis are heavily influenced by diet and lifestyle factors. Current management of GERD involves lifestyle modifications (e.g., weight loss, dietary changes) and pharmacologic agents like proton pump inhibitors (PPIs), histamine-2-receptor blockers (H2 B), antacids, and medications that affect gastrointestinal motility (Kröner et al., 2021). Background on Probiotics and Zinc: Probiotics are non-pathogenic microorganisms that, when administered in adequate amounts, offer several health benefits, including improvement in conditions associated with inflammation and gut health. Probiotics, often of the Lactobacillusand Bifidobacterium species, interact with gut microbiota, enhance barrier function, and modulate immune responses (Cheng & Ouwehand, 2020; Kröner et al., 2021). Probiotics have been linked to reduced levels of inflammatory mediators, such as cytokines, and are recognized for their anti-inflammatory and antioxidant properties (Sharifi-Rad et al., 2020; Wang et al., 2017). Zinc, specifically Zinc L-carnosine, exhibits antioxidant, cytokine modulation, and membrane-stabilizing properties, acting as a mucosal cytoprotective and anti-inflammatory agent (Efthymakis & Neri, 2022). Previous studies suggest that the combination of probiotics and zinc may be beneficial for gut health, but there is limited data on their effects on GERD symptoms, inflammation, and oxidative stress. Study Aim: To evaluate the effect of probiotics and zinc on GERD symptoms and to explore their potential antioxidant and anti-inflammatory effects. Patients and Methods: Study Design: This is a prospective controlled randomized comparative study conducted at El-Demerdash Hospital, Ain Shams University Hospitals. Ethical Considerations: The study has received ethical approval from the Research Ethics Committee of the Faculty of Pharmacy, Ain Shams University, and the Scientific Research Ethics Committee at the Faculty of Medicine, Ain Shams University. It adheres to the Declaration of Helsinki and is registered on ClinicalTrials.gov. Participants: Inclusion Criteria: Adults aged 18-74 years with esophagitis confirmed by gastroscopy and GERD symptoms. Exclusion Criteria: Allergy to study medications, pregnancy, severe renal or liver insufficiency, history of myocardial infarction, stroke, malignant tumors, and certain gastrointestinal conditions or surgeries. Sample Size Calculation: The study is designed to detect a large effect size (f = 0.4) for zinc and probiotic effects using G\*Power software. A total of 120 patients will be recruited (30 per group) to account for a 15% dropout rate. Study Groups: Group I (Control): PPI (Omeprazole 40 mg daily). Group II: PPI + probiotic. Group III: PPI + zinc. Group IV: PPI + probiotic and zinc. Methodology: Participants will undergo baseline assessments, including medical history, gastroscopy, and measurement of gastrointestinal hormones, inflammatory markers (IL-6, IL-12, CRP), and oxidative stress markers (MDA). The same assessments will be repeated at the study's end after 4 weeks. Follow-up assessments will occur biweekly, and patients will be contacted between visits to monitor side effects. Outcomes: Primary Outcome: Change in Gastrointestinal Symptom Rating Scale (GSRS) scores and gastrin hormone levels before and after treatment. Secondary Outcomes: Anti-inflammatory effect (IL-6, IL-12, CRP levels). Antioxidant effect (MDA levels). Statistical Analysis: Data will be analyzed using SPSS. Statistical significance is set at p ≤ 0.05. Continuous variables will be expressed as mean ± SD or median (interquartile range), depending on distribution, and analyzed using appropriate tests (e.g., T-test or Mann-Whitney U test). This study aims to provide insights into the potential benefits of probiotics and zinc in managing GERD symptoms and their anti-inflammatory and antioxidant effects, filling a current gap in the literature.

Interventions

It reduces stomach acid production and manage GERD symptoms

DRUGProbiotic

Live microorganisms, primarily bacteria and yeast, that are believed to provide health benefits when consumed in adequate.

DRUGZinc

Zinc used a supplement due to its role in decreasing inflammation of the gastroesophageal reflux disease.

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 74 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 18-74 years; (both male and female). * Esophagitis that might be confirmed by gastroscopy. * Patients with confirmed symptoms of GERD N.B.: The typical clinical presentation of GERD is heartburn and regurgitation. Heartburn is defined as a retrosternal burning sensation or discomfort that may radiate into the neck and typically occurs after the ingestion of meals or when in a reclined position. Regurgitation is a retrograde migration of acidic gastric contents into the mouth or hypopharynx . GERD can also present with various other symptoms that include dysphagia, odynophagia, belching, epigastric pain, and nausea.

Exclusion criteria

* Allergy or potential allergy to the study medications. * Pregnancy. * Patients with CrCl< 20 ml/min or on dialysis. * Patients with myocardial infarction, stroke, or malignant tumour. * Patients with liver insufficiency (liver enzymes > 2\*upper limit of normal) * Heart Failure or ECG (electrocardiogram) abnormalities * Gastroscopy that revealed any of the following diseases within the last 2 months: bleeding, esophageal and gastric varices, upper gastrointestinal malignant lesions. * A history of gastroesophageal or duodenal surgery.

Design outcomes

Primary

MeasureTime frameDescription
Change in Gastrointestinal Symptom Rating Scale (GSRS)1 month•The primary efficacy variable will be the change in Gastrointestinal Symptom Rating Scale (GSRS) score before and after treatment (reflecting the patient's experience of the dyspepsia symptoms during the preceding weeks: pain, heartburn, acid reflux, hunger, pain, nausea, stomach rumbles, stomach swelling, belching, bloating, constipation, diarrhea, and interchange between constipation and diarrhea) as well as the effect on gastrin hormone level.

Secondary

MeasureTime frame
Anti-inflammatory effect will be measured through the markers (Interleukin-6 (IL-6), Interleukin-12 (IL-12) and CRP levels.1 month
Antioxidant effect measured through oxidative stress marker as (MAD).1 month

Contacts

Primary ContactChristina M Aziz
christina.medhat@bue.edu.eg+201286750660

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026