Skip to content

The effect of rice soup in treatment of acute diarrhea

A comparison between the simultaneous consumption of Oral Rehydration Solution (ORS) along with rice soup and consuming ORS per se in the treatment of acute diarrhea in 6-24 months old children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201310169459N1
Enrollment
40
Registered
2014-01-07
Start date
2013-11-22
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

Acute Diarrhea. functional diarrhea

Interventions

Intervention 1: Intervention 1 in the control group: the patients in this group will receive ORS (produced by Hayan company, Iran) for treating diarrhea using the treatment recommended by WHO based on
Treatment - Other
Treatment - Drugs
Intervention 1 in the control group: the patients in this group will receive ORS (produced by Hayan company, Iran) for treating diarrhea using the treatment recommended by WHO based on which the requi
Intervention 2 in the intervention group: the patients in this group, in addition to ORS (produced by Hayan company, Iran), will receive rice soup till their dismissal from the hospital based on the t

Sponsors

Vice chancellor for research, Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 24 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: •Children between the ages of 6 and 24 months •Underlying disease may not be the cause of diarrhea. •More than 72 hours from the onset of diarrhea is passed. •The amount of serum sodium and potassium ions is in the normal range. •The patient does not consume the foods such as syrup, artificial ingredients, very sweet food, fruit juice, yogurt, butter milk, etc. that increase or decrease the severity of diarrhea. •The patient should continue with the diet. Exclusion criteria: • Regarding medicine, continuing the research is not possible for the patient. •The patient's parents are not willing to continue the investigation. •If the patient abandons the required diet during the dietary intervention. •If there is severe vomiting along with diarrhea.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The use rate of ORS solution. Timepoint: The first 24 hours, the second 24 hours, and the third 24 hours. Method of measurement: Determination of consumed volume by graded container.;The use rate of intravenous fluids. Timepoint: The first 24 hours, the second 24 hours, and the third 24 hours. Method of measurement: Observation.;Serum levels of Na and K ions. Timepoint: The onset of hospitalization, before any kind of intervention. Method of measurement: Blood collection and its experimenting with flame photometer.;Serum levels of Urea. Timepoint: The onset of hospitalization, before any kind of intervention and at the end of intervention, before discharge. Method of measurement: Blood collection and its experimenting through spectrophotometer.

Secondary

MeasureTime frame
Hospitalization stay. Timepoint: The end of intervention. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMojtaba Kianmehr

Gonabad University of Medical Sciences

kianmehr.m@gmu.ac.ir+98 53 3722 5027

Outcome results

None listed

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