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The effect of Omeprazole suspension on gastric pH of ICU patients

Evaluating the effect of prepared powder for Omeprazole suspension on gastric pH of ICU patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016062120592N6
Enrollment
30
Registered
2016-08-09
Start date
2015-07-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

erosion (acute) of stomach. Gastric ulcer

Interventions

patients for prophylaxis treated with omeprazol suspension (40mg)every day via nasogastric tube for 14 days. Gastric aspirates were sampled before(empty stomach) and 1.5-2 hours after administration o
Treatment - Drugs

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 95 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age of =16 yrs of age; anticipated stay of =72 hrs in ICU; required mechanical ventilation more than 48 hrs; APACHE II score =11; have a nasogastric or orogastric tube in place; have at least one additional risk factor for upper GI bleeding Exclusion criteria: status of no CPR; delay of >48 hrs from time of initial eligibility; history of gastric surgery; allergy to omeprazole; active GI bleeding; significant risk of swallowing blood; admission for upper GI surgery; known upper GI Lesions that might bleed; inability to take a suspension by nasogastric tube;end-stage liver disease

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Mean gastric pH. Timepoint: before and 1-2.5 hrs after drug administration. Method of measurement: pH meter.

Secondary

MeasureTime frame
Active upper GI bleeding. Timepoint: every day up to 14 days. Method of measurement: Gastroccult test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDoctor Fanak Fahimi

Shahid Beheshti University of Medical Sceinces,Faculty of pharmacy

fanakfahimi@yahoo.com+98 21 8820 0118

Outcome results

None listed

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