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Effect of probiotics on treating neonatal jaundice

Effect of probiotics with phototherapy in compare to phototherapy for reduction of bilirubin in term neonates

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017032333129N1
Enrollment
150
Registered
2017-05-30
Start date
2016-08-22
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

Neonatal jaundice. Neonatal jaundice, unspecified:Physiological jaundice (intense)(prolonged) NOS

Interventions

Intervention 1: Administration of probiotics to study group Pedilact drop from Zist Takhmir Company 10 drop/day. Intervention 2: control group is given only phototherapy.
Treatment - Drugs
Administration of probiotics to study group Pedilact drop from Zist Takhmir Company 10 drop/day
control group is given only phototherapy.

Sponsors

Babol University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 30 Days

Inclusion criteria

Inclusion criteria: Inclusion criteria : term; healthy; age less than 28 day and more than 1day;weight more than 2500 grams; Exclusion criteria : ABO incompatibility;Rh incompatibility; G6PD deficiency, weight below 2500 gr; history of exchange transfusion in previous sibling; use of drugs such as Phenobarbital during pregnancy; drug and home remedy for jaundice; gestational age less than 37 completed weeks;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Serum billirubin level in study group. Timepoint: At admission serum billirubin level. Method of measurement: mg/dl , device: bilitest A from tajhizat sanjesh company.;Serum billirubin level in study group. Timepoint: Second day serum billirubin level. Method of measurement: mg/dl , device: bilitest A from tajhizat sanjesh company.;Serum billirubin level in study group. Timepoint: Third day serum billirubin level. Method of measurement: mg/dl , device: bilitest A from tajhizat sanjesh company.;Serum billirubin level in study group. Timepoint: Forth day serum billirubin level. Method of measurement: mg/dl , device: bilitest A from tajhizat sanjesh company.;Serum billirubin level in contrl group. Timepoint: At admission serum billirubin level. Method of measurement: mg/dl , device: bilitest A from tajhizat sanjesh company.;Serum billirubin level in contrl group. Timepoint: Second day serum billirubin level. Method of measurement: mg/dl , device: bilitest A from tajhizat sanjesh company.;Serum billirubin level in contrl group. Timepoint: Third day serum billirubin. Method of measurement: mg/dl , device: bilitest A from tajhizat sanjesh company.;Serum billirubin level in contrl group. Timepoint: Forth day serum billirubin level. Method of measurement: mg/dl , device: bilitest A from tajhizat sanjesh company.

Secondary

MeasureTime frame
Duration of admission in control group. Timepoint: At discharge. Method of measurement: Day.;Need of blood exchang transfusion in control group. Timepoint: At discharge. Method of measurement: No.;Need of blood exchang transfusion in control group. Timepoint: At discharge. Method of measurement: Yes.;Need of blood exchang transfusion in study group. Timepoint: At discharge. Method of measurement: No.;Duration of admission in study group. Timepoint: At discharge. Method of measurement: Day.;Need of blood exchang transfusion in study group. Timepoint: At discharge. Method of measurement: Yes.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Abes Ahmadi Jazi

Babol University of Medical Science

Abesahmadijazi@yahoo.com+98 11 3234 2151

Outcome results

None listed

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