H.Pylori InfectionPhase 4NCT06315478
Safety and Efficacy of Triple and Quadruple Regimens as First Line Therapy for Management of Helicobacter Pylori Infection in Egyptians
A Phase 4 study testing Omeprazole 20 MG Oral Tablet, Amoxicillin 500Mg Tab and Clarithromycin 500Mg Tab in people with H.Pylori Infection, run by Helwan University at 1 site in Egypt.
Trial summary
Our study aimed to investigate the efficacy and safety of hybrid regimen as a first line therapy for H. pylori eradication compared to triple and quadruple regimens in attempt to overcome antibiotic resistance Read more about this study
- Who is it for?
- Ages 18 to 60 years
- Conditions the study is for
- H.Pylori Infection
- What is being tested?
- Omeprazole 20 MG Oral Tablet, Amoxicillin 500Mg Tab and Clarithromycin 500Mg Tab
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Feb 2021to 1 Nov 2021
- Phase
- Phase 4
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 60 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- 1. Naïve patients 2. adult >18 years 3. Patients with positive SAT 4. Patients didn't take any antibiotics for the previous 4 weeks or PPI for the previous 2 weeks 5. Patients diagnosed with duodenal ulcers who have H. pylori infection and treated with triple or quadruple regimens for H. pylori
Who cannot join
- 1-Patients had any concern with triple or quadruple regimens such as hypersensitivity to any of the drug 2-Pregnancy or lactation 3-Refusal to sign the informed consent.
Trial locations and contacts
1 site in 1 country.
About this study
Our study aimed to investigate the efficacy and safety of hybrid regimen as a first line therapy for H. pylori eradication compared to triple and quadruple regimens in attempt to overcome antibiotic resistance
Read the detailed description
Helicobacter pylori (H. pylori) is a globally prevalent pathogen which infects about over 50% of population. However, not all cases have clinical symptoms, H. pylori are described as gram negative bacteria which causes ulcers in the lining of stomach or the upper part of small intestine. For some patients, a progressive infection can cause gastric cancer which is the second widespread cancer worldwide (1).
While this pathogen in Egypt is a public health issue, the propagation of H. pylori infection is approximately 80% (2), study results concluded that H. pylori infection in upper Egypt was higher than in urban areas (3).
Transmission modes of H. pylori are very controversial, the reservoir of H. pylori is the human stomach. The main method of acquisition in both developing and developed countries by fecal oral route, whereas the other route of transmission in developed countries is the gastro-oral route mainly water borne prevalence, overcrowding of the family of large number members, institutionalized children are predisposing for acquiring the infection. (4:6), and occupational risk factor for health members, in particular those working in gastrointestinal units (7). Over spread of the infection in upper Egypt could be due to the hygiene level, socioeconomic conditions, life style, and absence of sources of pure water supply in rural areas (3).
- pylori has been classified as one of the 12 bacterial species need high priority future strategies for new antibiotic development by the World Health Organization (WHO), management of H. pylori is widely debatable due to high antibiotics resistance prevalence after exclusion of inadequate gastric suppression by proton pump inhibitor and poor adherence to the therapy. Furthermore, the efficacy of many regimens has declined due to increased antibiotic resistance making H. pylori eradication challenging, H. pylori treatment has been complicated and has required 10 and 14 days of multiple daily doses of three or four different medicines. (8:13).
There is no worldwide accepted regimen for the eradication of H. pylori infection. Standard triple therapy (STT) with proton pump inhibitors (PPI) in standard dose, clarithromycin (500 mg), and amoxicillin (1 g) twice daily for 14 days is the standard triple first line regimen in the published international guidelines of the European Helicobacter and Microbiota Study Group in areas of low clarithromycin resistance (14).
A randomized controlled trial in Japan showed that clarithromycin resistance is a growing problem found metronidazole to be superior to clarithromycin as a 7-day first-line triple regimen (15).
In regions with low dual clarithromycin and metronidazole resistance (<15%), either a bismuth quadruple therapy (BQT) (PPI, bismuth salt, tetracycline, and metronidazole) or non-bismuth concomitant quadruple therapy (PPI, amoxicillin, clarithromycin, and metronidazole) is recommended (14,16), In areas of high dual clarithromycin and metronidazole resistance (>15%), bismuth quadruple therapy is the recommended regimen. However, bismuth isn't available in all regions and not preferred due to complexity and the high pill burden (14 pills per day). Therefore, levofloxacin, rifabutin or high dose dual (amoxicillin and PPI) therapies have been suggested (14,17).
A levofloxacin triple therapy is recommended as second-line treatment in case of first line therapy failure; However, clarithromycin-based triple therapy or bismuth quadruple therapy are alternative second-line options if not used as first line regimen and clarithromycin resistance is known to be low.
Third-line and subsequent treatment strategies should be guided by antimicrobial susceptibility testing, treatment durations of 14 days and the use of newer generation PPIs are recommended in all H. pylori regimens, unless local evidence suggests that 10 days therapy is efficient (14,18,19). In Egypt, the first and second line H. pylori regimens as the international guidelines are used to eradicate H.pylori. However, these recommendations should be reviewed, due to increased resistance rate and progressive decline in eradication therapy efficacy. (20).
Expert groups in USA, Canada, and Europe have issued treatment guidelines for the management of H. pylori infection to overcome the global challenge of antibiotic resistance (13).
Treatment of H. pylori is still widely empiric due to antibiotic resistance, which could be prevented through culture guided therapy that associated with higher eradication rates (21,22).
Some experts such as the Maastricht guidelines recommend clarithromycin susceptibility testing before prescribing clarithromycin triple regimen or after second line regimen failure, its preferable to have this test in an earlier phase than waiting for two treatment failures mostly due to increased levofloxacin resistance, a component of many second line therapies (14,23,24).
Antibiotic susceptibility testing can be done by culture or molecular methods, both of which require gastric biopsies. However. This test is less cost-effective to be adopted widespread (23). The scarcity of such data in USA was an obstacle to make strong evidence-based treatment recommendations in the 2017 ACG guideline on H. pylori treatment (19).
In USA, only two publications in the previous 20 years including fewer than 500 strains of H. pylori have revealed resistance features (13,25,26) A recent study compared the efficacy of first-line H.pylori eradication therapies including STT, BQT, sequential therapy (ST) consisting of a PPI and amoxicillin for 5-7 days followed by a PPI, clarithromycin, and a metronidazole for 5-7 days, and HT. Results revealed that hybrid regimen had the best H.pylori eradication rates (27).
Another study compared the efficacy of different regimens for eradication of H. pylori had shown that A 14-day hybrid therapy has attracted global attention as this regimen proved to be safe, well tolerated and effective in high antibiotic resistance settings (28,29).
A current hybrid therapy (HT) (PPI and amoxicillin for 14 days followed by clarithromycin and a nitroimidazole for 7 days) is a promising first-line strategy for H. pylori eradication due to the rising prevalence of antibiotic resistance globally (30).
To the best of our knowledge there is lacking information about hybrid regimen efficacy in eradication of H.pylori infection in Egyptian patients, our study aimed to investigate the efficacy and safety of hybrid regimen as a first line therapy for H. pylori eradication compared to triple and quadruple regimens in attempt to overcome antibiotic resistance.
- Conditions
- H.Pylori Infection
- Being tested
- Omeprazole 20 MG Oral Tablet, Amoxicillin 500Mg Tab, Clarithromycin 500Mg Tab
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Omeprazole 20 MG Oral TabletDrug
Also called amoxicillin 500 mg, clarithromycin 500mg
standard triple therapy for 14 days Bid for each drug
Amoxicillin 500Mg TabDrug
Also called Omeprazole 20 MG Oral Tablet, clarithromycin 500mg, metronidazole 500mg
Quadruple regimen for 14 days Bid for each drug
Clarithromycin 500Mg TabDrug
Also called amoxicillin 500 mg Tablet, Omeprazole 20 MG Oral Tablet, metronidazole 500mg Tablet
Hybrid regimen, PPI and Amoxicillin for first 7 days then adding clarithromycin and metronidazole for the second 7 days
| Study group | Role | What they receive |
|---|---|---|
| Triple regimen(Group A) | Active comparator | Not described Receives: Drug: Omeprazole 20 MG Oral Tablet |
| Quadruple regimen (Group B) | Active comparator | Not described Receives: Drug: Amoxicillin 500Mg Tab |
| Hybrid regimen (Group C) | Active comparator | Not described Receives: Drug: Clarithromycin 500Mg Tab |
What is being measured
The primary outcome is the main question the study is designed to answer.
stool antigen retest
efficacy of the regimen by eradication of H. pylori
Measured: 6 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Mar 2024
- Study start1 Feb 2021
- Primary completion16 Mar 2021
- Study completion1 Nov 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for H.Pylori InfectionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Helwan University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Donia Mohamed Eid, Helwan University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06315478
- Sponsor's protocol ID
- Hybrid regimen for H.pylori
- Status last verified
- Mar 2024
- First submitted
- 11 Mar 2024
- Last updated
- 18 Mar 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 Mar 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Safety and Efficacy of Triple and Quadruple Regimens as First Line Therapy for Management of Helicobacter Pylori Infection in Egyptians
- ClinicalTrials.gov ID
- NCT06315478
- Acronym / sponsor ID
- Hybrid regimen for H.pylori
- Conditions
- H.Pylori Infection
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Helwan UniversityUniversity, hospital or other
- Study start
- 1 Feb 2021 (actual)
- Primary completion
- 16 Mar 2021 (actual)
- Study completion
- 1 Nov 2021 (actual)
- First posted
- 18 Mar 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Our study aimed to investigate the efficacy and safety of hybrid regimen as a first line therapy for H. pylori eradication compared to triple and quadruple regimens in attempt to overcome antibiotic resistance
Detailed description
Helicobacter pylori (H. pylori) is a globally prevalent pathogen which infects about over 50% of population. However, not all cases have clinical symptoms, H. pylori are described as gram negative bacteria which causes ulcers in the lining of stomach or the upper part of small intestine. For some patients, a progressive infection can cause gastric cancer which is the second widespread cancer worldwide (1).
While this pathogen in Egypt is a public health issue, the propagation of H. pylori infection is approximately 80% (2), study results concluded that H. pylori infection in upper Egypt was higher than in urban areas (3).
Transmission modes of H. pylori are very controversial, the reservoir of H. pylori is the human stomach. The main method of acquisition in both developing and developed countries by fecal oral route, whereas the other route of transmission in developed countries is the gastro-oral route mainly water borne prevalence, overcrowding of the family of large number members, institutionalized children are predisposing for acquiring the infection. (4:6), and occupational risk factor for health members, in particular those working in gastrointestinal units (7). Over spread of the infection in upper Egypt could be due to the hygiene level, socioeconomic conditions, life style, and absence of sources of pure water supply in rural areas (3).
- pylori has been classified as one of the 12 bacterial species need high priority future strategies for new antibiotic development by the World Health Organization (WHO), management of H. pylori is widely debatable due to high antibiotics resistance prevalence after exclusion of inadequate gastric suppression by proton pump inhibitor and poor adherence to the therapy. Furthermore, the efficacy of many regimens has declined due to increased antibiotic resistance making H. pylori eradication challenging, H. pylori treatment has been complicated and has required 10 and 14 days of multiple daily doses of three or four different medicines. (8:13).
There is no worldwide accepted regimen for the eradication of H. pylori infection. Standard triple therapy (STT) with proton pump inhibitors (PPI) in standard dose, clarithromycin (500 mg), and amoxicillin (1 g) twice daily for 14 days is the standard triple first line regimen in the published international guidelines of the European Helicobacter and Microbiota Study Group in areas of low clarithromycin resistance (14).
A randomized controlled trial in Japan showed that clarithromycin resistance is a growing problem found metronidazole to be superior to clarithromycin as a 7-day first-line triple regimen (15).
In regions with low dual clarithromycin and metronidazole resistance (<15%), either a bismuth quadruple therapy (BQT) (PPI, bismuth salt, tetracycline, and metronidazole) or non-bismuth concomitant quadruple therapy (PPI, amoxicillin, clarithromycin, and metronidazole) is recommended (14,16), In areas of high dual clarithromycin and metronidazole resistance (>15%), bismuth quadruple therapy is the recommended regimen. However, bismuth isn't available in all regions and not preferred due to complexity and the high pill burden (14 pills per day). Therefore, levofloxacin, rifabutin or high dose dual (amoxicillin and PPI) therapies have been suggested (14,17).
A levofloxacin triple therapy is recommended as second-line treatment in case of first line therapy failure; However, clarithromycin-based triple therapy or bismuth quadruple therapy are alternative second-line options if not used as first line regimen and clarithromycin resistance is known to be low.
Third-line and subsequent treatment strategies should be guided by antimicrobial susceptibility testing, treatment durations of 14 days and the use of newer generation PPIs are recommended in all H. pylori regimens, unless local evidence suggests that 10 days therapy is efficient (14,18,19). In Egypt, the first and second line H. pylori regimens as the international guidelines are used to eradicate H.pylori. However, these recommendations should be reviewed, due to increased resistance rate and progressive decline in eradication therapy efficacy. (20).
Expert groups in USA, Canada, and Europe have issued treatment guidelines for the management of H. pylori infection to overcome the global challenge of antibiotic resistance (13).
Treatment of H. pylori is still widely empiric due to antibiotic resistance, which could be prevented through culture guided therapy that associated with higher eradication rates (21,22).
Some experts such as the Maastricht guidelines recommend clarithromycin susceptibility testing before prescribing clarithromycin triple regimen or after second line regimen failure, its preferable to have this test in an earlier phase than waiting for two treatment failures mostly due to increased levofloxacin resistance, a component of many second line therapies (14,23,24).
Antibiotic susceptibility testing can be done by culture or molecular methods, both of which require gastric biopsies. However. This test is less cost-effective to be adopted widespread (23). The scarcity of such data in USA was an obstacle to make strong evidence-based treatment recommendations in the 2017 ACG guideline on H. pylori treatment (19).
In USA, only two publications in the previous 20 years including fewer than 500 strains of H. pylori have revealed resistance features (13,25,26) A recent study compared the efficacy of first-line H.pylori eradication therapies including STT, BQT, sequential therapy (ST) consisting of a PPI and amoxicillin for 5-7 days followed by a PPI, clarithromycin, and a metronidazole for 5-7 days, and HT. Results revealed that hybrid regimen had the best H.pylori eradication rates (27).
Another study compared the efficacy of different regimens for eradication of H. pylori had shown that A 14-day hybrid therapy has attracted global attention as this regimen proved to be safe, well tolerated and effective in high antibiotic resistance settings (28,29).
A current hybrid therapy (HT) (PPI and amoxicillin for 14 days followed by clarithromycin and a nitroimidazole for 7 days) is a promising first-line strategy for H. pylori eradication due to the rising prevalence of antibiotic resistance globally (30).
To the best of our knowledge there is lacking information about hybrid regimen efficacy in eradication of H.pylori infection in Egyptian patients, our study aimed to investigate the efficacy and safety of hybrid regimen as a first line therapy for H. pylori eradication compared to triple and quadruple regimens in attempt to overcome antibiotic resistance.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Triple regimen(Group A) | Active comparator | Drug: Omeprazole 20 MG Oral Tablet |
| Quadruple regimen (Group B) | Active comparator | Drug: Amoxicillin 500Mg Tab |
| Hybrid regimen (Group C) | Active comparator | Drug: Clarithromycin 500Mg Tab |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (1 listed)
- 1. Naïve patients 2. adult >18 years 3. Patients with positive SAT 4. Patients didn't take any antibiotics for the previous 4 weeks or PPI for the previous 2 weeks 5. Patients diagnosed with duodenal ulcers who have H. pylori infection and treated with triple or quadruple regimens for H. pylori
Key exclusion criteria (1 listed)
- 1-Patients had any concern with triple or quadruple regimens such as hypersensitivity to any of the drug 2-Pregnancy or lactation 3-Refusal to sign the informed consent.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Omeprazole 20 MG Oral TabletAlso: amoxicillin 500 mg, clarithromycin 500mgstandard triple therapy for 14 days Bid for each drug | Drug | Triple regimen(Group A) |
| Amoxicillin 500Mg TabAlso: Omeprazole 20 MG Oral Tablet, clarithromycin 500mg, metronidazole 500mgQuadruple regimen for 14 days Bid for each drug | Drug | Quadruple regimen (Group B) |
| Clarithromycin 500Mg TabAlso: amoxicillin 500 mg Tablet, Omeprazole 20 MG Oral Tablet, metronidazole 500mg TabletHybrid regimen, PPI and Amoxicillin for first 7 days then adding clarithromycin and metronidazole for the second 7 days | Drug | Hybrid regimen (Group C) |
Primary outcome
stool antigen retest
Time frame: 6 weeks
efficacy of the regimen by eradication of H. pylori
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Mar 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Omeprazole 20 MG Oral Tablet, Amoxicillin 500Mg Tab and Clarithromycin 500Mg Tab in people with H.Pylori Infection, run by Helwan University at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 18 Mar 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
stool antigen retest (time frame: 6 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Mar 2024; AzTrials last refreshed its copy on 8 Nov 2026.