MedDataX Logo

Fast Tracking Impact on Fentanyl Consumption and Parents Satisfaction

NCT ID: NCT04376541

Last Updated: 2020-05-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

70 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-01-01

Study Completion Date

2020-04-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The investigators are measuring fentanyl consumption in micrograms used during anesthesia for patients on fast track congenital cardiac surgeries

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Efficacy of iv Fentanyl Citrate Administered Oral as a Pediatric Premedication

NCT04991298

Anesthesia, Local
UNKNOWN NA

Effect of Topical Airway Block on Hemodynamic Stability Post Induction of Anaesthesia in Cardiac Surgeries

NCT06395727

Cardiac Surgery
COMPLETED PHASE4

Effects on Recovery of Children of Intravenous Formulation of Fentanyl Citrate and Midazolam Orally for Premedication

NCT05500599

Separation Anxiety
ACTIVE_NOT_RECRUITING NA

Cardioprotective Effect of Ketamine-dexmeditomidine Versus Fentanyl-midazolam in Open Heart Surgery in Pediatrics

NCT05314569

Anesthesia
COMPLETED PHASE1

Is it Possible to Replace Fentanyl in Anesthesia for Minor Procedures?

NCT03806374

Anesthesia
COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The investigators are measuring fentanyl consumed for both fast track and conventional corrective cardiac surgeries and also parents Parental Perceptions satisfaction with early child communication in ICU and impact of caudal anesthesia on extubation time our 2ry outcomes are the hospital and ICU length of stay

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Fentanyl Adverse Reaction Caudal Anesthesia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

early extubation

the patients extubated in O.R or within 2 hours in the ICU

Fentanyl

Intervention Type DRUG

amount of fentanyl used in both groups

late extubation

the patients extubated after 2 hours from O.R

Fentanyl

Intervention Type DRUG

amount of fentanyl used in both groups

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Fentanyl

amount of fentanyl used in both groups

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* patients diagnosed with congenital cardiac anomaly for surgical correction.
* age limit: child 3months of age to 18 years

Exclusion Criteria

patients with any o the following:

* emergency surgeries
* redo surgeries
* complex surgeries
* patients weight less than 3kg
Minimum Eligible Age

3 Months

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Gamal Adel Adelhameed

lecturer of anesthesia and intensive care and pain management

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

s 43

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Pharmacokinetics and Pharmacodynamics of Oral Transmucosal Dexmedetomidine.
NCT03120247 COMPLETED PHASE2/PHASE3
Fentanyl Versus Midazolam as an Adjunct to Intrathecal Bupivacaine In Children
NCT03592537 COMPLETED PHASE2/PHASE3
Dexmedetomedine Infusion Versus Fentanyl Infusion for Donor Anlgesia During Living Donor Hepatectomy
NCT02531529 COMPLETED NA
Evaluation of the Postoperative Agitation Prevention and Analgesic Efficacy of Perioperative Dexmedetomidine Infusion in a Pediatric Patient Group to Undergo Tonsillectomy and Adenoidectomy
NCT05986942 COMPLETED
Effect of Dexmedetomidine and Propofol on Regional Cerebral Tissue Oxygen Saturation
NCT03817112 COMPLETED NA
Comparison of Nebulized Fentanyl, Midazolam and Dexmedetomidine as a Premedication in Pediatric Dental Surgeries
NCT04226885 COMPLETED NA
Effect of Nebulized Milrinone on Right Ventricular Hemodynamics in Adult Cardiac Surgery
NCT05132153 UNKNOWN PHASE4
Comparison of Propofol-fentanyl and Midazolam-fentanyl for Conscious Sedation
NCT01749579 UNKNOWN PHASE4
Subtenon and Intravenous Dexmedetomidine Effect on Patients Undergoing Cataract Surgery
NCT04668456 UNKNOWN PHASE3
Dexmedetomidine Versus Fentanyl Added to Levobupivacaine for Transversus Abdominis Plane (TAP) Block
NCT03778671 COMPLETED PHASE1/PHASE2
Dexmedetomidine and Fentanyl As Adjuvants to Hyperbaric Bupivacaine for the Prevention of Post-spinal Shivering in Hip Arthroplasty Surgeries
NCT06834841 RECRUITING NA
Attenuation of Airway and Cardiovascular Responses to Extubation in Chronic Smokers
NCT04659642 UNKNOWN EARLY_PHASE1
Dexmedetomidine Versus Fentanyl for Sedation of Postoperative Mechanically Ventilated Neonates
NCT05324891 COMPLETED PHASE2
Dexmedetomidine in Spinal Anesthesia Decreasing Post Spinal Shivering in Caesarean Section
NCT06318546 COMPLETED PHASE1
Comparative Study of Fentanyl vs Dexmedetomidine as Adjuvants to Intrathecal Bupivacaine in Cesarean Section
NCT06785285 COMPLETED NA
Intrathecal Additives to Prevent Post Spinal Shivering in Transurethral Prostatectomy
NCT04178512 UNKNOWN NA
Dexmedetomidine as an Adjunct to Fentanyl for Term Neonates on Mechanical Ventilation
NCT07241351 COMPLETED PHASE2/PHASE3
Comparsion of IV Dexmedetomidine, Tramdol and Ketamine for Post Spinal Anesthesia Shivering.
NCT05311722 UNKNOWN PHASE3
The Effect of Opioid Free Anesthesia in Bariatric Surgeries
NCT04048200 COMPLETED PHASE4
Comparison of Intrathecal Dexmedetomidine Versus Fentanyl as Adjuvants to Bupivacaine on Post-operative Urinary Retention in Knee Joint Arthroscopic Surgeries
NCT05596552 COMPLETED PHASE4
Dexmedetomidine-propofol-remifentanil Anaesthesia and Reactivity to Noxious Stimuli
NCT01076790 COMPLETED PHASE4
Pre-medication With Alfentanil vs Placebo During ECT
NCT03359395 COMPLETED PHASE4
Clinical Comparative Study Aiming to Evaluate Postoperative Effect of Using Intrathecal Dexmedetomidine and Fentanyl as an Adjuvant to Heavy Bupivacaine in Lower Limb Vascular Surgeries on Pain Intensity, Analgesic Requirement and Shivering. Patients and Methods After Approval of Medical Institution
NCT07035223 COMPLETED PHASE4
Analgesic and Sedative Effect of Fentanyl Versus Dexmedetomidine Infusion in Post-Operative Mechanically Ventilated Children After Open Abdominal Surgeries
NCT06994273 COMPLETED NA
Ketamine Versus Fentanyl for Induction of Anesthesia in Septic Shock
NCT03251170 COMPLETED PHASE4