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Efficacy of JINLINGGUAN and TOFER Formula in Formula-fed Chinese Term Infants

Efficacy of JINLINGGUAN and TOFER Formula in Formula-fed Chinese Term Infants: A Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03178474
Enrollment
180
Registered
2017-06-07
Start date
2015-12-01
Completion date
2017-12-30
Last updated
2017-09-18

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

Conditions

Infant Formula Intolerance, Well-being

Keywords

infant formula, Clinical trial, Chinese infant, body growth, gut microbiota, Stool characteristics

Brief summary

Objective:The present trial aimed to assess efficacy and safety of Jin Ling Guan and Tofer infant formula on body growth, intestinal tolerance, gut microbiota and fecal residual nutrients as compared to breast-milk in term Chinese infants. Participants:189 healthy termed-infants with ages of 5-14 days at the enrollment. Study Design: A multiple-center, quasi-randomized,open labeled, controlled trial. Random allocation between the two infant formula. Arms, Groups, and Intervention: (1) Breast milk-fed group: fed with human breast milk; (2) JINLINGGUAN Formula Group:fed with JINLINGGUAN infant formula (PRO-KIDO™ I-PROTECH®, Phase I); (3) TOFER Formula Group: feeding TOFER infant formula (TOFER®, Phase I). Random allocation performed between the two formula groups. Intervention Duration: 12 weeks. Visits: 1 week(baseline), 7 and 13 weeks of age Outcome measures: (1) General information, general health and wellbeing, regular body check;(2) Anthropometric parameters: body length, body weight, and head circumferences; (3) Stool characteristics (color , volume, stool consistency, and frequency;(4)Behavior and habits; (5) Gut microbiota; (6) Residual nutrients in feces (nitrogen,total fat, fatty acids, minerals); (7) adverse events and concomitant medications; (8) compliance. Slopes of changes from baseline to 6 and 12 weeks post intervention in anthropometric parameters, stool characteristic index, fecal residual nutrients, pattern score of gut microbiota, behavior and habit index were be calculated.

Interventions

OTHERJINLINGGUAN Infant formula,PRO-KIDO™ I-PROTECH®

JINLINGGUAN Infant formula,PRO-KIDO™ I-PROTECH®: a type of Phase I infant formula for 0-6 month infants, with a trademark of PRO-KIDO™ I-PROTECH®. The formula contains both OPO structured lipid and α+β patented protein (patent number: ZL200810241156.3).It was produced by Inner Mongolia Yili Industrial Group Co.Ltd.,China

OTHERTOFER Infant formula,TOFER®

TOFER Infant formula,TOFER®: a type of Phase I infant formula for 0-6 month infants, with a trademark of TOFER®. The formula was characterized by (1) Moderate digestible small-molecule protein; and (2) BID® complex probiotics. It was produced by Inner Mongolia Yili Industrial Group Co.Ltd.,China

OTHERBreast milk

Breast milk: Human breast milk, provided and fed by the corresponding infant's mother

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

Researchers involved in laboratory tests will be blinded to the group status

Eligibility

Sex/Gender
ALL
Age
5 Days to 14 Days
Healthy volunteers
Yes

Inclusion criteria

* The mother had unequivocally decided not to breast-feed (for formula fed infants) or to breastfeed (for human milk fed infants) * Term infant of Chinese origin born at 37-42 gestation weeks * Birth weight: 2500-4000g * The infant is apparently healthy at birth and entry to study * Apgar after 5 minutes \>7 * age at the enrollment: 5-14 days

Exclusion criteria

* Mother health condition: (psychological or physical) or socioeconomic problems that may interfere with the mother's ability to take care of her infant * The infant suffers from a major congenital abnormality or chromosomal disorder with a clinical significance that can be detected at birth * The infant suffers/ed from a disease requiring mechanical ventilation or medication treatment at the first week after birth (not including photo treatment for infantile hepatitis) * The infant suffers from any suspected or known metabolic or physical limitations interfering with feeding or normal metabolism

Design outcomes

Primary

MeasureTime frameDescription
Average Change Rate of Fecal Residual Calcium from Baseline to 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in fecal residual calcium
Average Change Rate of Fecal Residual Fat from Baseline to 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in fecal residual total fat
Average Change Rate of Stool Characteristic Index from Baseline to 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in Stool Characteristic Index: calculated using stool color (using sample pictures), volume (small, normal or large using sample picture scale), stool consistency (runny, mushy, soft, formed or hard), and frequency
Average Change Rate of Fecal Residual Nitrogen from Baseline to 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in Fecal Residual Nitrogen

Secondary

MeasureTime frameDescription
Average Change Rate of Body Weight from Baseline to 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in body weight
Average Change Rate of Gut Microbiota Pattern Score from Baseline at 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in gut microbiota pattern score from 16S RNA sequencing
Average Change Rate of Pattern Score of Fecal Residual Fatty acids from Baseline at 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in the pattern score of fecal residual fatty acids
Average Change Rate of Head Circumference from Baseline to 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in head circumference
Average Change Rate of an Index of General health and wellbeing from Baseline to 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in Index of General health and wellbeing, calculated from diseases (cold, diarrhea, bronchitis, pneumonia), doctor visits, gastro symptoms,etc.
Average Change Rate of Behavior and Habit Score from Baseline to 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in Behavior and Habit Score assessed by infant behavior questionnaires
Average Change Rate of body length from Baseline to 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in body length

Other

MeasureTime frameDescription
Average Change Rate of Fecal Residual Iron from Baseline at 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in fecal residual iron
Average Change Rate of Fecal Residual Zinc from Baseline at 6 and 12 weeks0, 6, 12 weeksSlope of change at 0, 6 and 12 weeks in fecal residual zinc

Countries

China

Contacts

Primary ContactYuming Chen, Ph.D.
chenyum@mail.sysu.edu.cn8613710230430
Backup ContactQian Zhou
zhouq83@mail.sysu.edu.cn862087330726

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026