Bismuth Based Quadruple Therapy 10 Days in Children

NCT ID: NCT03299725

Last Updated: 2018-02-15

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 120 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-11-24
• Study Completion Date: 2019-11-30

Brief Summary

Helicobacter pylori infection causes chronic gastritis, peptic ulcer disease and is involved in the development of gastric cancer.

Current accepted strategies to eliminate the infection in children are a 10 days sequential treatment (proton pump inhibitor + amoxicillin 5 days followed by proton pump inhibitor + metronidazole + clarithromycin 5 days) or a triple therapy 14 days (proton pump inhibitor + amoxicillin + clarithromycin or metronidazole).

However, there is a concern due to the growing resistance of Helicobacter pylori strains to antibiotics, especially clarithromycin, and the decreased efficacy of first line treatment regimens to satisfactorily eliminate the infection in children.

Recent data show that combinations using bismuth salts must be considered in adults. Indeed, the efficacy of a 10 days of quadruple therapy with omeprazole plus a single three-in-one capsule containing bismuth subcitrate, metronidazole and tetracycline was shown to be highly superior to the standard triple therapy combining omeprazole, amoxicillin, and clarithromycin without related severe adverse events.

The possibility of re-using bismuth salts on a more regular basis in pediatrics is being restudied through a monocentric, prospective, open label, single arm clinical trial to assess the safety and efficacy of a 10 days colloidal bismuth sub-citrate as an adjunctive therapy in combination with esomeprazole, amoxicillin and metronidazole in children aged 6-17 years, infected by Helicobacter pylori.

Conditions

Helicobacter Pylori Infection

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment arm

Group Type: EXPERIMENTAL

colloidal bismuth sub-citrate

Intervention Type: DRUG

colloidal bismuth sub-citrate administered as an adjunctive therapy in combination with esomeprazole, amoxicillin and metronidazole

Interventions

colloidal bismuth sub-citrate

colloidal bismuth sub-citrate administered as an adjunctive therapy in combination with esomeprazole, amoxicillin and metronidazole

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Paediatric subjects aged 6 to 17 years of either gender
• Body weight ≥ 20kg.
• Helicobacter pylori gastritis confirmed by positive histology and culture with antimicrobial susceptibility testing.
• Antral and corpus biopsies must have been taken for histology and culture during an upper GI endoscopy performed for chronic or recurrent pain in the epigastric region with epigastric tenderness at physical examination.
• Subject able to swallow tablets.
• All girls of child-bearing potential must have a negative urine pregnancy test at Visit 1. If sexually active, girls of child-bearing potential and boys whose partner is of child-bearing potential agree to use highly effective method of birth control during the trial.
• In the Investigator's opinion, patient is willing and able to comply with all trial requirements specified in this protocol.
• Willing to allow his or her General Practitioner and consultant, if appropriate, to be notified of participation in the trial.
• Subjects (or their legally-acceptable representatives) must have signed an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study. Assent is also required of children capable of understanding the nature of the study (typically older than 11 years of age).

Exclusion Criteria

• Female participant who is pregnant, lactating or planning pregnancy during the course of the trial.
• Have a history of significant renal or hepatic impairment.
• Have an erosive esophagitis or peptic ulcer disease in the gastric or the duodenal mucosa showed during the upper GI endoscopy.
• Have received proton pump inhibitors within 2 weeks prior to first administration of study agent.
• Have received any antimicrobial agent within 4 weeks prior to first administration of study agent.
• Require routine use (≥ 2 times per week) of non-steroidal anti-inflammatory drug (NSAID).
• Are under any immunosuppressive agent.
• Are under oral or IV steroids
• Have a scheduled elective surgery or any procedures requiring general anaesthesia during the trial.
• Have known allergies or a known hypersensitivity to any Study Drugs or their excipients (refer to Study Drugs SmPCs).
• Contraindication for any of the Study Drugs (refer to Study Drugs SmPCs).
• Any condition that, in the opinion of the investigator, would compromise the well-being of the subject or the study or prevent the subject from meeting or performing study requirements.
• Subjects who are participating or have participated in another study with an IMP in the past 12 weeks.

• Minimum Eligible Age: 6 Years
• Maximum Eligible Age: 17 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Queen Fabiola Children's University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Abdallah Kanfaoui, MD

Role: STUDY_DIRECTOR

Queen Fabiola Children's University Hospital

Locations

Hôpital Universitaire Des Enfants Reine Fabiola

Brussels, , Belgium

Site Status: RECRUITING

Countries

Belgium

Central Contacts

Samy Cadranel, MDPhD

Role: CONTACT

samy.cadranel@huderf.be

0032 2 477 32 16

Patrick Bontems, MDPhD

Role: CONTACT

patrick.bontems@huderf.be

0032 2 477 32 16

Facility Contacts

Samy Cadranel, MDPhD

Role: primary

samy.cadranel@huderf.be

003224773216

Other Identifiers

CBS-EAM 10d

Identifier Type: -

Identifier Source: org_study_id