Gastritis Clinical Trial
— RASATHEMEOfficial title:
Open Label, Randomized, Single Site Clinical Trial To Compare The Safety Of Herbal Melanin Extracted From Nigella Sativa Seeds Vs Standard Of Care Treatment In Treating Gastritis Patients
The aim of the study is to use Melanole, a herbal extract from Nigella sativa, for treatment
of gastritis. The effect of Melanole will be compared between participants (including H.
pylori and non-H.pylori infected patients), with the triple therapy and Standard of care
treatment of gastritis, respectively.
All participants will be examined before and after the administration of Melanole. The
results showing a relief of gastritis symptoms for non-H. pylori patients and partial or
complete eradication of H. pylori for H.pylori infected patients will be evaluated.
Status | Not yet recruiting |
Enrollment | 132 |
Est. completion date | March 2020 |
Est. primary completion date | March 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: - Males or Females between 18- 60 years - Willing to sign Informed Consent Form (ICF) - Women of Child bearing age will be asked to conduct a pregnancy test before enrolling in the study and offered contraceptives for the duration of the study participation - Clinical Pictures of Gastritis. - Histologically confirmed H- Pylori Gastritis or Non H- Pylori by one week from enrollment. Exclusion Criteria: - Patients with disturbed gastrointestinal physiology (gastric surgery, vagotomy, Zollinger-Ellison syndrome) - Patients who have been treated with proton pump inhibitors during 3 weeks prior to inclusion - Patients who have been treated with antibiotics or bismuth containing drugs 1 month prior enrolling in the study - Patient with pyloric stenosis - Patient with Hematologic disorder - Patient with congestive heart disease - Women who are pregnant or lactating - Current or past history of malignancy - Drug abuser and chronic alcoholism - Patients currently participating in any other clinical trial of any kind |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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King Abdullah International Medical Research Center |
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* Note: There are 29 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of participants cured from acidity symptoms and H.Pylori -induced gastritis | Investigators hypothesize that HM is an effective candidate that can decrease stomach acidity and eradicate H.Pylori by working as Proton Pump Inhibitor(PPI) and/or antibacterial agent, respectively. Investigators suggest the role of HM in activation of Toll like Receptor 4 (TLR4)/Cycloxygenase2(COX2)/ProstaglandinE2( PGE2) as one underlying mechanism. | 6 months | |
Secondary | Number of Participants cured with herbal melanin as compared to number of participants cured with standard of care for gastritis and H.Pylori-induced gastritis | Gastritis as indicated by improving the clinical presentation of gastritis and confirmed by end of treatment endoscopy and stool antigen test | 6 months | |
Secondary | Number of Participants between study groups having high expression of TLR4 and COX2 as assessed by Western blots procedure. | By using stomach biopsies for measuring the expression of TLR4 and COX 2 expression. | 6 months |
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