Preemptive Analgesia for Post Tonsillectomy Pain With IV Morphine in Children

Sponsor
Dr. Soliman Fakeeh Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT02995304
Collaborator
(none)
60
1
2

Study Details

Study Description

Brief Summary

In this double blind study, after taking an informed consent, 60 children aged between 7 and 12 years old assigned for tonsillectomy with or without adenoidectomy will be randomly divided into three groups. The first group 30 children will receive 0.025 mg/kg midazolam IV followed by 0.1 mg/kg morphine as a premedication 20 to 30 min before surgical incision. In the second group30 children who will receive the same dose of midazolam followed by saline premedication. All groups will be compared for pain score using visual analog scale (VAS) after recovery and hourly for 8 hours and during first drinking. Heart rate (HR), blood pressure and peripheral oxygen saturation (SPO2) will be recorded before premedication, every 10 min after premedication then every 5 min during and after anesthesia. 6 point sedation score and 4 points behavioral score will be monitored every 5 min after sedation. Four-point wake-up score will be recorded every 5 min. Time of first analgesic requirement and total morphine consumption during the first post-operative 8 hours will be recorded.

Condition or Disease Intervention/Treatment Phase
  • Drug: Morphine premedication
  • Drug: Midazolam premedication
  • Drug: Saline premedication (placebo)
N/A

Detailed Description

Tonsillectomy is a minor procedure but it causes sever post-operative pain. This pain is difficult to be controlled with opioids because the fear from respiratory depression in pediatric age group with postoperative oral bleeding. The World Heath Organization (WHO) guidelines clearly state that fear and lack of knowledge regarding the use of opioids in children should not be a barrier for effective analgesia (1). ). However, these procedures are usually day case and the use of oral morphine at home may be risky in some groups of this population (2). So decrease the analgesic requirements following these procedures will increase both satisfaction and safety. The trials for the use of morphine as a preemptive analgesia, in awake patient, have been limited to intramuscular (IM) or oral use which has a slow onset and unpredictable absorption. The use of preoperative IV morphine is not popular because of the unpleasant sensations following its administration. I will use small dose midazolam 0.025 gm/kg before morphine to prevent this sensation. In this double blind study, after taking an informed consent, 60 children aged between 7 and 12 years old assigned for tonsillectomy with or without adenoidectomy will be randomly divided into three groups. The first group 30 children will receive 0.025 mg/kg midazolam IV followed by 0.1 mg/kg morphine as a premedication 20 to 30 min before surgical incision. In the second group30 children who will receive the same dose of midazolam followed by saline premedication. Inhalational anesthesia with sevoflurane and nitrous oxide will be used in all patients. Exclusion criteria are those with bronchial asthma, obstructive sleep apnea, allergy to medications used in the study and those who are unfit for surgery or anesthesia for any reason like coagulopathy or chest infection.

All groups will be compared for pain score using visual analog scale (VAS) after recovery and hourly for 8 hours and during first drinking. HR, blood pressure and SPO2 will be recorded before premedication, every 10 min after premedication then every 5 min during and after anesthesia. 6 point sedation score and 4 points behavioral score will be monitored every 5 min after sedation. Four-point wake-up score will be recorded every 5 min. Time of first analgesic requirement and total morphine consumption during the first post-operative 8 hours will be recorded. Base line oxygen saturation, incidence of postoperative hypoxia, bleeding, nausea and vomiting will be recorded.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Preemptive Analgesia for Post Tonsillectomy Pain With IV Morphine in Children
Study Start Date :
Dec 1, 2016
Anticipated Primary Completion Date :
Mar 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Morphine and Midazolam premedication

30 children will receive 0.025 mg/kg midazolam IV followed by 0.1 mg/kg morphine 20 to 30 min before surgical incision.

Drug: Morphine premedication
30 children will 0.1 mg/kg morphine as a premedication 20 to 30 min before surgical incision.

Drug: Midazolam premedication
All children who will receive 0.025 mg/kg midazolam IV as a premedication 20 to 30 min before surgical incision.

Active Comparator: Midazolam only premedication

30 children who will receive 0.025 mg/kg midazolam IV followed by saline 20 to 30 min before surgical incision.

Drug: Midazolam premedication
All children who will receive 0.025 mg/kg midazolam IV as a premedication 20 to 30 min before surgical incision.

Drug: Saline premedication (placebo)
30 children in midazolam only group will receive saline after midazolam

Outcome Measures

Primary Outcome Measures

  1. Postoperative morphine requirement [8 hours]

Secondary Outcome Measures

  1. Postoperative nonsteroidal analgesic requirements [two days]

  2. Preoperative behavior score [15 to 30 minutes]

    B. Behavior scores: 1 - Calm and cooperative 2 - Anxious but can be reassured 3 - Anxious and can not be reassured 4 - Crying, or resisting C. Wake-up behavior scores 1 - Calm and cooperative 2 - Not calm but could be easily calmed 3 - Not easily calmed, moderately agitated or restless 4 - Combative, excited, disoriented.

  3. Wake-up behavior scores [30 minutes]

Eligibility Criteria

Criteria

Ages Eligible for Study:
7 Years to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Tonsillectomy procedures in

  • Children aged between 7 and 12 years old.

Exclusion Criteria:

Bronchial asthma, obstructive sleep apnea, allergy to medications used in the study and those who are unfit for surgery or anesthesia for any reason like coagulopathy or chest infection.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Doctor Soliman Fakeeh Hospital Jeddah Saudi Arabia 21461

Sponsors and Collaborators

  • Dr. Soliman Fakeeh Hospital

Investigators

  • Principal Investigator: Amr A Keera, MD, Doctor Soliman Fakeeh Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Amr Aly Ismail Keera, Principle investigator, Dr. Soliman Fakeeh Hospital
ClinicalTrials.gov Identifier:
NCT02995304
Other Study ID Numbers:
  • 03/IRB/2016
First Posted:
Dec 16, 2016
Last Update Posted:
Dec 16, 2016
Last Verified:
Dec 1, 2016
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 16, 2016