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Oral sucrose + soother group (group A) for Pain

N/A
Recruiting
Led By Adel Mohamed, MD
Research Sponsored by Mount Sinai Hospital, Canada
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights

Study Summary

This trial will study the effects of oral sucrose and soother versus soother alone on pain management and its outcomes in premature infants during lung ultrasound scans.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Premature infant pain profile Score (PIPP) measured in (points 0-21) ranging 0-21 points
Secondary outcome measures
Total time to complete the scan (minutes)

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Oral sucrose + soother group (group A)Experimental Treatment1 Intervention
Group A: Infants will receive oral sucrose (24%) followed by a soother 2 minutes before the procedure "LUS scan". The dose will be 0.2 mL, 0.5 mL and 1 mL for infants with current weight < 1500g, 1500-2500g, and > 2500g respectively.
Group II: Soother alone group (group B)Active Control1 Intervention
Group B (control group): infants will receive a soother 2 minutes before LUS scan.

Find a Location

Who is running the clinical trial?

Mount Sinai Hospital, CanadaLead Sponsor
194 Previous Clinical Trials
67,340 Total Patients Enrolled
4 Trials studying Pain
587 Patients Enrolled for Pain
Adel Mohamed, MDPrincipal InvestigatorSinai Health System
2 Previous Clinical Trials
105 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is my profile compatible with the conditions for taking part in this examination?

"Eligible candidates for this clinical trial are those suffering from pain and aged between 0 Days to 37 Weeks. A total of 64 participants will be recruited into the study."

Answered by AI

Does this clinical investigation accept geriatric participants?

"This clinical trial necessitates that patients be between 0 Days and 37 Weeks old to qualify for enrollment."

Answered by AI

Are recruitment efforts still underway for this research project?

"Affirmative. According to clinicaltrials.gov, this medical research is actively seeking participants, with the first post dating back to December 18th 2020 and last update on January 30th 2023. The trial is searching for 64 volunteers at a single site."

Answered by AI

How many individuals have signed up for participation in this experiment?

"Affirmative, according to the records on clinicaltrials.gov this study is actively searching for participants with a start date of December 18th 2020 and an edit made as recent as January 30th 2023. The trial has 1 site aiming to enroll 64 patients in total."

Answered by AI
~15 spots leftby Mar 2025