Combination With Intranasal Dexmedetomidine and Oral Midazolam for Premedication in Pediatric Patients

Anxiety Clinical Trial

Official title:

Intranasal Dexmedetomidine or Oral Midazolam Alone Versus Combination With Intranasal Dexmedetomidine and Oral Midazolam for Premedication in Pediatric Patients Undergoing Minor Surgery

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04135014
• Other study ID #: SAHoWMU-CR2019-03-111
• Status: Recruiting
• Phase: Phase 4
• Start date: October 25, 2019
• Est. completion date: October 2020

Study information

• Verified date: November 2019
• Source: Second Affiliated Hospital of Wenzhou Medical University
• Contact: Huacheng Liu
• Phone: 18957755138
• Email: huachengliu[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Children tend to anxiety and even fear before survey. And this kind of anxiety will not result in the forced induction of anesthesia, but also may increase the incidence of postoperative agitation in children, even lead to postoperative behavior changes.Currently,Oral midazolam or intranasal dexmedetomidine alone is commonly used as a preoperative regimen, but the clinical effects of each single-use are not satisfactory. In the investigators' study，the researchers conducted the current study to investigate whether dexmedetomidine combined with midazolam can increase the rate of satisfactory anesthesia induction in pediatric patients and achieve better sedative effect.

Description:

A trained member of the research team obtained a baseline The Modified Yale Preoperative Anxiety Scale(mYPAS) after obtaining consent. And corresponding study medication is administered about 30-40 minutes before the anesthesia induction.Vital signs were measured every 5 min after study medication administration.The sedation scores of the children were recorded with University of Michigan Sedation Scale (UMSS) every 10 minutes.The onset time of satisfactory sedation and parental separation anxiety scale was noted.Then recorded the degree of cooperation during inhalation anesthesia induction and recovery times.Moreover, recorded the pediatric anesthesia emergence delirium scale (PAED) during the recovery period.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 138
• Est. completion date: October 2020
• Est. primary completion date: October 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 2 Years to 6 Years

Eligibility

Inclusion Criteria:

1. with American Society of Anesthesiologists (ASA) physical status I or II;

2. aged 2-6 years;

3. children with weight for age within the normal range

4. were scheduled lower abdominal and perineal surgery with an expected operation time shorter than 30 minutes.

Exclusion Criteria:

1. Children who had gastrointestinal,Cardiovascular or endocrine dysfunction;

2. contraindication to preoperative sedation or had a known allergy or hypersensitive reaction to either dexmedetomidine or midazolam;

3. with any nasal pathology,organ dysfunction;

4. recently respiratory infection, mental disorder;

5. other reasons that researchers hold it is not appropriate to participate in this trial.

Related Conditions & MeSH terms

• Anxiety

Intervention

Drug:
• Midazolam
oral midazolam 0.5mg.kg-1 approximately 30-40 minutes before surgery using a computer-generated random number table.
• Dexmedetomidine
intranasal dexmedetomidine 2µg.kg-1 approximately 30-40 mins before surgery using a computer-generated random number table.
• Midazolam and Dexmedetomidine
oral midazolam 0.5mg.kg-1 and intranasal dexmedetomidine 1ug.kg-1 approximately 30-40 mins before surgery using a computer-generated random number table.

Locations

Country	Name	City	State
China	The second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University	Wenzhou	Zhejiang

Sponsors (1)

Lead Sponsor	Collaborator
Second Affiliated Hospital of Wenzhou Medical University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The degree of cooperation during inhalation anesthesia induction	Induction Compliance Checklist range from 0 through 10,and lower scores indicate the higher degree of cooperation during inhalation anesthesia induction	During inhalation anesthesia induction
Secondary	Anxiety before induction of anesthesia	The Modified Yale Preoperative Anxiety Scale: The 22-item measure has five behavioural categories: activity, emotional expressivity, alertness and arousal, vocalizations, and interaction with parents. Total scores range from 23.33 through 100 with higher scores indicating greater anxiety.	Before preoperative medication
Secondary	The level of sedation	University of Michigan Sedation Scale: 0 -Awake/Alert; 1 -Minimally Sedated: Tired/sleepy, appropriate response to verbal conversation and/or sounds.; 2- Moderately Sedated: Somnolent/sleeping, easily aroused with light tactile stimulation.; 3 - Deeply Sedated: Deep sleep, arousable only with significant physical stimulation.; 4 - Unarousable.; higher scores mean a higher levels of sedation.	Each 10 minutes during the preoperative period
Secondary	The onset time of satisfactory sedation	The onset time of satisfactory sedation, defined as the time from drug administration to the time when the University of Michigan Sedation Scale reached two points.; University of Michigan Sedation Scale: 0 -Awake/Alert; 1 -Minimally Sedated: Tired/sleepy, appropriate response to verbal conversation and/or sounds.; 2- Moderately Sedated: Somnolent/sleeping, easily aroused with light tactile stimulation.; 3 - Deeply Sedated: Deep sleep, arousable only with significant physical stimulation.; 4 - Unarousable.; higher scores mean a higher levels of sedation.	During the preoperative period
Secondary	Parental separation anxiety scale	A four-point parental separation anxiety scale as follows: -Easy separation,; -Whimpers, but is easily reassured, not clinging,; - Cries and cannot be easily reassured, but not clinging to parents,; - Crying and clinging to parents.; The scores of 1 and 2 signified acceptable separation whereas scores of 3 and 4 were classified as difficult separation.	During the preoperative period
Secondary	Recovery times	The time from discontinuation of sevoflurane to the first open eye of the children and to achieve aldrete=9	Within up to 30 minutes after child's first eye opening in the postoperative period
Secondary	Pediatric anesthesia emergence delirium	The pediatric anesthesia emergence delirium scale consists of four items. Each item is scored 0-4 yielding a total between 0 and 20.; The degree of emergence delirium increased directly with the total score.pediatric anesthesia emergence delirium scale =12 at any time indicates presence of emergence delirium.	Within up to 15-30 minutes after child's first eye opening in the postoperative period
Secondary	Number of children with adverse effects	Number of children with adverse effects; Bradycardia and/or hypotension need for hemodynamic support; Desaturation is defined as Oxygen desaturation <90%; Salivation; Any adverse effects requiring interventions	Up to 24 hours including preoperative, intraoperative, and postoperative periods