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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06065839
Other study ID # 202201089A3
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 20, 2022
Est. completion date August 16, 2024

Study information

Verified date October 2023
Source Chang Gung Memorial Hospital
Contact Yu-Ting HUANG, BSN
Phone +886975832680
Email Bunny@cgmh.org.tw
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The design of this study is an experimental research design, and the research subjects who meet the conditions of acceptance will be used as randomized controlled trials. Cases meeting the sampling conditions in the neonatal intensive care unit were stratified according to birth weeks (26 to 27+6 weeks and 28 to 31+6 weeks), and then randomly assigned to experimental group A (non-nutritive sucking 5 minutes), experimental group B (non-nutritive sucking for 15 minutes) and control group (no non-nutritive sucking). The variables controlled in this study were gestational weeks, birth weight, sex, Apgar score, respirator use, and type of milk fed. The premature infants in the experimental group were given non-nutritive sucking before the first tube-feeding and the feeding volume reached 10mL/kg/day, while the control group was not given non-nutritive sucking before tube-feeding. The interventional measures adopted in this study were set as two meals a day before 17:00, and the patients were force-fed every three hours, and the time interval between the two interventional measures was every six hours (intervention measures were provided every other meal) , the measurement time, times and intervals of the two groups are the same. Experimental group A was given pacifier NNS 5 minutes before each feeding, experimental group B was given pacifier NNS 15 minutes before each feeding, while the control group was not given NNS before feeding, and the two groups were given 150 minutes after feeding (ie 30 minutes before the next force-feeding) to monitor gastric residual volume, changes in abdominal circumference, and vomiting. Since FI mainly occurred 48-72 hours after the start of feeding, the duration of this study was 3 consecutive days to compare with the control group. The acceptance conditions of the research objects are: 1. Premature infants whose gestational age is more than 26 weeks (inclusive) to less than 32 weeks, 2. Premature neonates who have been placed with orogastric tube or nasogastric tube for force-feeding, 3. No congenital gastrointestinal tract Abnormal, 4. No serious congenital abnormalities and heart disease, no cleft lip and palate, 5. Never received stomach or intestinal surgery, 6. No central nervous system damage, 7. With the consent of their parents or guardians, and fill out the consent form By. If the condition is unstable during the course of the case, including severe hypoxemia, hypotension, esophageal perforation, necrotic enteritis, sepsis caused by infection, and grade 3-4 intraventricular hemorrhage, etc., they will be excluded.


Recruitment information / eligibility

Status Recruiting
Enrollment 180
Est. completion date August 16, 2024
Est. primary completion date August 16, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 26 Weeks to 32 Weeks
Eligibility Inclusion Criteria: - Premature infants whose gestational age is more than 26 weeks (inclusive) to less than 32 weeks - Premature neonates who are force-fed with orogastric or nasogastric tubes - No congenital gastrointestinal abnormalities - No serious Congenital anomalies and heart disease, no cleft lip and palate - Never received stomach or intestinal surgery - No central nervous system damage - With the consent of their parents or guardians, and fill out the consent form. Exclusion Criteria: - Severe hypoxemia - Severe hypotension - Esophageal perforation - Necrotic enteritis - Infection-induced sepsis - 3-4 grades of ventricular hemorrhage

Study Design


Related Conditions & MeSH terms


Intervention

Other:
non-nutritive sucking 5 minutes
Give pacifier non-nutritive sucking for 5 minutes before feeding
non-nutritive sucking 15 minutes
Give pacifier non-nutritive sucking for 15 minutes before feeding

Locations

Country Name City State
Taiwan Chang Gung Memorial Hospital Taoyuan Kwei-Shan District

Sponsors (1)

Lead Sponsor Collaborator
Chang Gung Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

References & Publications (5)

Bernbaum JC, Pereira GR, Watkins JB, Peckham GJ. Nonnutritive sucking during gavage feeding enhances growth and maturation in premature infants. Pediatrics. 1983 Jan;71(1):41-5. — View Citation

Foster JP, Psaila K, Patterson T. Non-nutritive sucking for increasing physiologic stability and nutrition in preterm infants. Cochrane Database Syst Rev. 2016 Oct 4;10(10):CD001071. doi: 10.1002/14651858.CD001071.pub3. — View Citation

Marchini G, Lagercrantz H, Feuerberg Y, Winberg J, Uvnas-Moberg K. The effect of non-nutritive sucking on plasma insulin, gastrin, and somatostatin levels in infants. Acta Paediatr Scand. 1987 Jul;76(4):573-8. doi: 10.1111/j.1651-2227.1987.tb10523.x. — View Citation

Szabo JS, Hillemeier AC, Oh W. Effect of non-nutritive and nutritive suck on gastric emptying in premature infants. J Pediatr Gastroenterol Nutr. 1985 Jun;4(3):348-51. doi: 10.1097/00005176-198506000-00004. — View Citation

Widstrom AM, Marchini G, Matthiesen AS, Werner S, Winberg J, Uvnas-Moberg K. Nonnutritive sucking in tube-fed preterm infants: effects on gastric motility and gastric contents of somatostatin. J Pediatr Gastroenterol Nutr. 1988 Jul-Aug;7(4):517-23. doi: 1 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary feeding intolerance Gastric residual volume in milliliter The test was carried out twice a day, with an interval of 6 hours between each data collection, and the test was carried out continuously for 3 days
Primary feeding intolerance abdominal circumference in centimeter The test was carried out twice a day, with an interval of 6 hours between each data collection, and the test was carried out continuously for 3 days
Primary feeding intolerance vomiting in frequency The test was carried out twice a day, with an interval of 6 hours between each data collection, and the test was carried out continuously for 3 days
See also
  Status Clinical Trial Phase
Completed NCT04095702 - Weighted Pacifier Vs. Non-Weighted Pacifier N/A
Recruiting NCT03801785 - Efficacy of Non-Nutritive Sucking (NNS) on Balance and Gait Measured in 12-42 Month-Old Healthy Children Over 36 Months N/A