Effect of Gabapentin in treatment of feeding refusal disorder

Phase 3

Recruiting

• Conditions: lnfants feeding refusal disorder.; Feeding difficulties; R63.3

• Registration Number: IRCT20190410043224N4
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 64

Inclusion Criteria

Age 3 to 6 months
The score of reflux questionary 16 or lower
Lack of an acute or chronic disease

Exclusion Criteria

The score of the reflux questionary greater than 16
Presence of an acute or chronic disease
Starting of complementary foods

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
umber of effective breastfeeding. Timepoint: At the beginning of the study and at the end of the second week and the first month. Method of measurement: The number of feedings from the mother's breast that lasts at least 10 minutes or the mother feels empty breasts and the volume of formula to cc.;Volume of formula consumed. Timepoint: Before the intervention, the end of the second week and the end of the first month. Method of measurement: Frequency of breastfeeding that lasts at least 10 minutes or the mother feels empty breasts-volume of formula consumed in mililiter.

Secondary Outcome Measures

Name	Time	Method
Restlessness. Timepoint: The end of the first months. Method of measurement: Asking from mother.