The Effect of Vitamin D Supplement as Adjuvant Therapy in Eradication of Helicobacter Pylori Infection
- Conditions
- Helicobacter Pylori Infection
- Interventions
- Registration Number
- NCT06964334
- Lead Sponsor
- Assiut University
- Brief Summary
Helicobacter pylori (H. pylori) is one of the most common chronic infections worldwide. The mode of transmission of H. pylori is through the fecal-oral or oral-oral routes.
Chronic gastritis has been linked to helicobacter pylori (H. pylori) infection. Peptic ulcer disease, gastric adenocarcinoma, and gastric lymphoma are all linked to this condition .
In Egypt, a high prevalence of H. pylori infections has been reported, ranging from 70% in the general population , 73% among school children , up to 88% in patients with chronic active HCV .
In 2007, the American College of Gastroenterology estimated that the cure rate for H. pylori infections was 70-85 percent with the use of a proton pump inhibitor (PPI), clarithromycin, and amoxicillin or metronidazole .
children with H. pylori infection do not have severe digestive symptoms. pylori infection represents a key factor in the pathogenesis of duodenal ulcer and chronic gastritis in children. In addition, H. pylori infection has also been reported to have extra-digestive consequences .
A recent comprehensive evaluation found that sequential and conventional triple treatment had a cure rate of 84% .
The infected macrophage is unable to create enough 1,25-(OH)2D to control the synthesis of AMP cathelicidin when it is vitamin D deficient .
vitamin D has a powerful systemic antibacterial impact by enhancing the activity of monocytes and macrophages. Most illnesses seem to benefit from a vitamin D-rich condition .
Vitamin D-deficient subjects might be more prone to developing H. pylori infection .
- Detailed Description
To assess the efficacy of adding vitamin D supplement as adjuvant therapy in eliminating helicobacter pylori infection.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 70
- Patients aged between 1 to 16 years old who present with helicobacter pylori infection diagnosed by positive stool antigen test for helicobacter pylori infection presented with weight loss, abdominal pain, or failure to surive symptoms for at least 1 month.
-
- Known hypersensitivity to PPIS or antibiotics. 2. Patients who have previously received helicobacter pylori eradication treatment, corticosteroids/immunosuppressive treatment and acid suppressive treatment in the prior 2 months.
- History of systemic inflammatory or autoimmune disorders, gastric surgery, renal failure, liver cirrhosis and malignancies 4. Abnormal birth history such as premature birth and asphyxia or with severe disease history, such as genetic metabolic disease, congenital dysplasia, feeding difficulties, severe malnutrition, repeated respiratory diseases.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Group A Lansoprazole include 35 patients with helicobacter pylori infection with clarithromycin based triple therapy and vitamin D supplement. Group A amoxicillin include 35 patients with helicobacter pylori infection with clarithromycin based triple therapy and vitamin D supplement. Group A clarithromycin include 35 patients with helicobacter pylori infection with clarithromycin based triple therapy and vitamin D supplement. Group A vitamin D include 35 patients with helicobacter pylori infection with clarithromycin based triple therapy and vitamin D supplement. Group B Lansoprazole include 35 patients with helicobacter pylori infection with clarithromycin based triple therapy and without vit D supplement. Group B amoxicillin include 35 patients with helicobacter pylori infection with clarithromycin based triple therapy and without vit D supplement. Group B clarithromycin include 35 patients with helicobacter pylori infection with clarithromycin based triple therapy and without vit D supplement.
- Primary Outcome Measures
Name Time Method cure rate after treatment 3 months compare cure rate between two groups
- Secondary Outcome Measures
Name Time Method