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The effect of omeprazole on pediatric chest pain

Evaluation of responses to Omeprazole treatment in children with non-cardiac chest pain

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191208045655N1
Enrollment
144
Registered
2019-12-25
Start date
2018-12-06
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-cardiac Chest Pain. Chest pain, unspecified

Interventions

Intervention 1: Intervention group: A course of treatment with omeprazole at a dose of 1mg / kg daily is prescribed for one week before breakfast for two weeks. Intervention 2: Control group: A placeb

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 18 Years

Inclusion criteria

Inclusion criteria: Kids 5-18 years old Complain chest pain that lasts for at least 2 weeks

Exclusion criteria

Exclusion criteria: cardiac chest pain Patient unwillingness to continue collaborating in the study Duration of pain more than 8 weeks History of trauma to the chest point tenderness

Design outcomes

Primary

MeasureTime frame
Chest pain. Timepoint: First, seventh and fourteenth days. Method of measurement: Visual Analogue Scale of pain.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVahid Heydari

Arak University of Medical Sciences

vahid.heidari8818@gmail.com+98 86 3367 5904

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026