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comparing crystaloids

Clinical trial study of comparison of normal saline and lactated ringer for fluid therapy in emergency department of Imam Reza hospital

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181105041562N1
Enrollment
1300
Registered
2018-11-19
Start date
2018-12-22
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

patients of emergency department of general hospitals that receive intravenous fluid. Dehydration

Interventions

Intervention 1: Intervention group: Normal Saline group: patients in this group receive normal saline. volume and speed of fluid will be prescribed by responsible physician that is not dependent of ty

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to No maximum

Inclusion criteria

Inclusion criteria: all patients of emergency department that fluid prescribed for them age more than 14

Exclusion criteria

Exclusion criteria: contraindication to each of these two fluids (according to FDA guideline) need to another fluid for patient need to infusion of drugs that can't infused with one of these fluids

Design outcomes

Primary

MeasureTime frame
In hospital death. Timepoint: discharge time. Method of measurement: based on hospital record.;Duration of hospitalization. Timepoint: at the end of hospitalization. Method of measurement: based on hospital record.;Creatinine clearance. Timepoint: 6 and 24 hours after initiation of IV fluid. Method of measurement: creatinine clearance estimated by the Cockcroft-Gault equation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Aliee

Kermanshah University of Medical Sciences

alialiee@gmail.com+98 83 3825 2948

Outcome results

None listed

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