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Glycerin Suppositories for Premature Infants
N/A
Waitlist Available
Led By J M Walton, M.D.
Research Sponsored by McMaster University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* Gestational age 24-32 weeks OR * Birth weight 500-1500 grams
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
All Individual Drugs Already Approved
Summary
This trial is testing glycerin suppositories in premature babies to help their bowels work better and prevent serious infections. The study will begin with a small group of babies to determine if a larger trial is feasible.
Who is the study for?
This trial is for premature infants born between 24-32 weeks of gestation or those with a birth weight of 500-1500 grams. It aims to help prevent feeding and digestive problems, including a serious bowel infection called necrotizing enterocolitis.
What is being tested?
The study is testing if glycerin suppositories can stimulate the digestive system in premature babies to prevent complications. Babies will be randomly given either a real glycerin suppository or a sham (fake) one as part of the pilot study at McMaster University Medical Centre.
What are the potential side effects?
Potential side effects may include mild discomfort or irritation where the suppository is inserted. Since this is a preliminary study, part of its purpose is to assess safety and any other possible side effects.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Secondary study objectives
Days to complete meconium evacuation
Other study objectives
Completion rate
Recruitment rate
Treatment-related adverse events
Awards & Highlights
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Glycerin SuppositoryActive Control1 Intervention
Group II: Sham SuppositoryPlacebo Group1 Intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Feeding intolerance in neonates, especially preterm infants, can lead to severe complications like necrotizing enterocolitis (NEC). Treatments such as glycerin suppositories stimulate the digestive tract, promoting bowel movements and reducing stasis, which helps in the timely passage of enteral feeds and reduces the risk of bacterial overgrowth and infection.
This is crucial for preventing NEC and ensuring better nutrient absorption. Other treatments may include prokinetics to enhance motility and careful management of feeding volumes and schedules to help the immature gut adapt gradually.
Gestational and postnatal maturation of duodenal motor responses to intragastric feeding.Gastrointestinal motility in the neonate.Two weeks of repetitive gut-challenge reduce exercise-associated gastrointestinal symptoms and malabsorption.
Gestational and postnatal maturation of duodenal motor responses to intragastric feeding.Gastrointestinal motility in the neonate.Two weeks of repetitive gut-challenge reduce exercise-associated gastrointestinal symptoms and malabsorption.
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Who is running the clinical trial?
McMaster UniversityLead Sponsor
916 Previous Clinical Trials
2,615,229 Total Patients Enrolled
McMaster Surgical AssociatesOTHER
16 Previous Clinical Trials
46,489 Total Patients Enrolled
Hamilton Health Sciences CorporationOTHER
377 Previous Clinical Trials
340,370 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My baby was born weighing between 500-1500 grams or was 24-32 weeks gestational age.
Research Study Groups:
This trial has the following groups:- Group 1: Glycerin Suppository
- Group 2: Sham Suppository
Awards:
This trial has 1 awards, including:- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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