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Efficacy of iv Fentanyl Citrate Administered Oral as a Pediatric Premedication

Efficacy of the Intravenous Formulation of Fentanyl Citrate Administered Orally as Premedication in Paediatric Patients Undergoing Open Cardiac Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04991298
Enrollment
60
Registered
2021-08-05
Start date
2021-06-01
Completion date
2022-07-25
Last updated
2021-08-05

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

Conditions

Anesthesia, Local

Brief summary

evaluate the efficacy of the intravenous formulation of fentanyl citrate administered orally as a sedative premedication, we will compare it with oral midazolam, as a gold standard premedication, in paediatric congenital cardiac surgeries

Detailed description

In this double-blinded randomized controlled study, after approval by the local ethics committee, paediatric patients, aged 1 to 7 years, scheduled for elective surgical procedures for correction of congenital heart disease will be enrolled. Patients with hepatic or renal disorders, gastrointestinal tract disorders or malformation, conduction disorders, coronary artery disease, emergency operations, mental disabilities, and known reactions to the drugs to be used will be excluded. After assessing the patient for anaesthesia, informed consent of patients about study and anaesthesia will be obtained.Children will be kept off solid food for 6 hours and of clear fluids for 2 hours. The premedication will be administered orally mixed with equal volume of 5% dextrose and using a 5-ml syringe, 30 minutes before admission to operating room by a member of the nursing staff unaware of the group allocation, in the preoperative holding area, in the presence of one parent. A randomized block design will be used for allocation of patients into two groups (50 patients each); one group of patients will receive midazolam (Group M) and the other will receive fentanyl (Group F) as a sedative premedication. 1. Group M: patients will be premedicated with the undiluted IV formulation of Midazolam (5 mg/mL), 0.5 mg/kg up to 15 mg per patient. The dose is chosen to be similar to the dose of midazolam used in other previous studies (). 2. Group F: patients will be premedicated with the undiluted IV formulation of fentanyl citrate (50 µg/mL), 10 µg/kg up to 400 µg per patient. The dose is chosen to be similar to the dose of OTFC used in other previous studies

Interventions

DRUGOral premedication

Oral anesthesia premedication for congenital Cardiac surgery

Sponsors

University of Alexandria
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
1 Years to 7 Years
Healthy volunteers
No

Inclusion criteria

* paediatric congenital heart disease patients, aged 1 to 7 years, scheduled for elective surgical procedures for correction of congenital heart disease

Exclusion criteria

* Patients with hepatic or renal disorders, gastrointestinal tract disorders or malformation, conduction disorders, coronary artery disease, emergency operations, mental disabilities, and known reactions to the drugs to be used will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Patient's acceptance of the medication (score from 1 to 3)1 yearResponse of the child to acceptance of premedication will be assessed on a three-point scale: 1. = Spits/vomits the premedication. 2. = Accepts it/but dislikes the taste. 3. = Accepts it/likes the taste.
Reaction to separation from parents (score from 1 to 4)1 yearThe response of the children when taken away from the parents will be recorded as the end point of premedication. It will be assessed on a four point scale: 1. = Inconsolable cry. 2. = Complaining. 3. = Quiet but awake. 4. = Sleepy.
Sedation score ( score from 1 to 6)1 yearThe degree of sedation, when the child will be first seen in the operating room (OR), will be scaled from 1 to 6 according to the Ramsay Sedation Scale. 1. =Anxious and agitated or restless, or both. 2. =Cooperative, oriented, and calm. 3. =Responsive to commands only. 4. =Exhibiting brisk response to light glabellar tap or loud auditory stimulus. 5. =Exhibiting a sluggish response to light glabellar tap or loud auditory stimulus. 6. =Unresponsive.
Ease of Induction of general anaesthesia (score from 1 to 4)1 yearA 4-point scoring system will used to evaluate the child's behaviour at anaesthesia induction and mask acceptance 1= Calm and cooperating 2 =Anxious but without resistance 3 =Anxious with slight resistance 4 =Crying and/or struggling against mask

Secondary

MeasureTime frameDescription
Hemodynamic effects1 yearHeart rate (beats/min)
Adverse effects1 yearnausea, vomiting, illusion, pruritis, paradoxical hyperactive reactions

Countries

Egypt

Contacts

Primary ContactIbrahim Mabrouk, Phd
ibrahim_wama@hotmail.com00201224336786
Backup ContactIslam Elbardan, Phd
Islamelbardan@gmail.com+20 111 227 8083

Outcome results

None listed

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