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Helicobacter Pylori InfectionEarly Phase 1NCT05100446

Comparison Between High-dose Amoxicillin Dual Therapy and Pylera Quadruple Therapy in the Treatment of Helicobacter Pylori Infection

A Early Phase 1 study testing Amoxicillin - high dose dual therapy, Pylera and Esomeprazole 40mg in people with Helicobacter Pylori Infection and Gastritis, run by Unidade Local de Saúde do Alto Ave, EPE at 1 site in Portugal.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Helicobacter pylori is a pathogenic bacteria transmitted from individual to individual, being scientifically recognized as an agent who causes persistent inflammatory activity on the gastric mucosa. This pathogen represents a Global Health problem, as shown in a systematic review by Hooi et al. Read more about this study

Who is it for?
Ages 18 to 75 yearsHealthy volunteers can take part
What is being tested?
Amoxicillin - high dose dual therapy, Pylera and Esomeprazole 40mg
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 sitePortugal
Study dates
1 May 2021to 31 Dec 2022
Phase
Early Phase 1
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 75 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Documented Helicobacter pylori infection
  • Age equal or greater to 18 years
  • Recent (<6months) upper digestive endoscopy
  • Ability to consent to participate in the study

Who cannot join

  • Documented allergy to any of the available drugs
  • Contraindications to any of the available drugs
  • Antibiotics use for the last 4 weeks
  • Previous gastric cancer
  • Previous gastric surgery
  • Pregnancy
  • Breastfeeding

Trial locations and contacts

1 site in 1 country.

Portugal1 site, 1 recruiting
  • Vítor Bruno Macedo da Silva

    Guimarães, 4835-044

    Vítor Bruno Macedo Silva, M.D., 00351253540330, vitorbmacedo@gmail.com

    Recruiting

Other trials in Portugal

About this study

Official title: Prospective Randomized Trial: Comparison Between High-dose Amoxicillin Dual Therapy and Pylera Quadruple Therapy in the Treatment of Helicobacter Pylori Infection

Helicobacter pylori is a pathogenic bacteria transmitted from individual to individual, being scientifically recognized as an agent who causes persistent inflammatory activity on the gastric mucosa. This pathogen represents a Global Health problem, as shown in a systematic review by Hooi et al. Besides regional differences, more that half of the world population is expected to have already been infected by this bacteria.

In Portugal, research studies estimate that more than 80% of the adult population has already contacted with H. pylori.

Read more
  1. pylori infection is associated with active chronic gastritis in every colonized patient, what may consequently lead to peptic ulcer disease, atrophic gastritis, gastric adenocarcinoma and mucosa-associated lymphoid tissue (MALT) lymphoma.

For that reason, H. pylori infection is considered to be a disease, independently of the presence of gastrointestinal symptoms. Additionally, H. pylori has been classified as a confirmed carcinogen (class I) by the International Agency for Research, being responsible for carcinogenic pathways conducting to both gastric adenocarcinoma and lymphoma. This fact gains a particular relevance taking into account that gastric cancer is one of the most prevalent cancers worldwide. On other hand, more than 75% of the gastric cancers occur following H. pylori infection.

Thus, H. pylori eradication constitutes an essential Public Health measurement, being inclusively considered a cost-effective method to decrease the gastric cancer burden, by promoting pre-malignant lesions regression, such as atrophic gastritis, and by delaying the disease progression in case of intestinal metaplasia or dysplasia.

Maastricht V consensus is a document updated in 2016, including the major recommendations regarding H. pylori diagnosis, follow-up and treatment. It highlights the emergence of antibiotic resistances and how they must influence clinical practice, namely the choice of antibiotic regimens, as successful eradication has become less frequent with more prevalent antibiotic resistances. This is the case of clarithromycin and metronidazol, both currently recommended as first-line options by the Portuguese Society of Gastroenterology. In fact, a systematic review conducted in 2018, aiming to evaluate antibiotic resistances on the Portuguese population observed that clarithromycin, metronidazole and double resistance occurred in 42%, 25% and 20% of the individuals, respectively.

Nowadays, Maastricht V guidelines recommend quadruple regimens containing bismuth, such as Pylera (r), as the first-line option in areas with significant double resistance to metronidazole and clarithromycin. Another option currently being investigated is the double therapy with amoxicillin in high doses and proton pump inhibitor. This has become a particularly attractive alternative due to its efficacy, good tolerability and significantly low resistance (<1%) among the European population.

The aim of this clinical trial is to compare both regimens - pylera (r) and high-dose amoxycillin - in H. pylori eradication, regarding their efficacy, tolerability and side effects, in order to asses viable therapeutic options in a population with progressively increasing resistances to alternative regimens currently recommended.

Being tested
Amoxicillin - high dose dual therapy, Pylera, Esomeprazole 40mg
Medical subject headings
Gastritis, Stomach Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Amoxicillin - high dose dual therapyDrug

    Eradication with Amoxicillin 1000mg + 500 mg + 1000mg + 500mg, for 15 days.

  • PyleraDrug

    Eradication with Pylera, for 10 days.

  • Esomeprazole 40mgDrug

    Esomeprazole 40mg, twice a day.

Study groups in NCT05100446
Study groupRoleWhat they receive
Treatment with Pylera (r) + esomeprazole 40mgActive comparatorNot described
Receives: Drug: Pylera; Drug: Esomeprazole 40mg
Treatment with high-dose amoxicillin + esomeprazole 40mgActive comparatorNot described
Receives: Drug: Amoxicillin - high dose dual therapy; Drug: Esomeprazole 40mg

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Helicobacter pylori eradication

    Confirmation of H. pylori eradication

    Measured: Approximately 1 month after treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Oct 2021
  2. Study start1 May 2021
  3. Primary completion31 Dec 2021 (estimated)
  4. Study completion31 Dec 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05100446
Sponsor's protocol ID
101/2020
Status last verified
Oct 2021
First submitted
19 Oct 2021
Last updated
29 Oct 2021
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A Early Phase 1 study testing Amoxicillin - high dose dual therapy, Pylera and Esomeprazole 40mg in people with Helicobacter Pylori Infection and Gastritis, run by Unidade Local de Saúde do Alto Ave, EPE at 1 site in Portugal.

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 4 inclusion and 7 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: status not confirmed, as of the sponsor's last update on 29 Oct 2021. 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 Portugal. 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?

Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Helicobacter pylori eradication (time frame: Approximately 1 month after treatment). 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 29 Oct 2021.

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