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Ketamine-ketorolac Versus Fentanyl- Ketorolac I.M in Children During Bone Marrow Biopsy

Analgesic Efficacy of Intra-muscular Ketamine-ketorolac Versus Fentanyl- Ketorolac for Children Undergoing Bone Marrow Biopsy and Aspiration

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03649334
Enrollment
80
Registered
2018-08-28
Start date
2018-08-26
Completion date
2018-10-15
Last updated
2020-09-09

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

Conditions

Hematological Malignancy (Leukemia- Lymphoma)

Brief summary

investigators aim to compare between anaesthetic regimens that included dual-agent (fentanyl and ketorolac) or (ketamine and ketorolac) analgesic therapy

Detailed description

regarding patient registry; a prior G power analysis was done. Based on the assumption that the pain score in intramuscular ketamine group will be similar to similar to those in previously published data; forty children would be required per group to detect a difference of 30% in CHEOPS pain scores with a power of 90% (α =0.05, β =0.1) \- Statistical analysis: Data will be analyzed through SPSS (Statistical Package for Social Sciences), program version 22. Distribution of data will be first tested by the Shapiro test. Data will be presented as the mean and standard deviation (SD), median and range or numbers and percentages. For normally distributed data, the unpaired t-test will be used to compare the mean values of both groups. For pain and emergence behaviour scores, Mann Whitney U test will be used. Fisher's exact test will be used for comparison of categorical data. The P value ≤ 0.05 will be considered as the level of statistical significance.

Interventions

DRUGketamine-ketorolac

The patient will receive ketamine 0.5mg.kg-1 + ketorolac 1mk.kg-1 in 2 ml syringe intramuscularly.

DRUGfentanyl- ketorolac

The patient will receive fentanyl 1.5ug.kg-1 + ketorolac 1 mg.kg-1 in 2ml syringe intramuscularly

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Caregiver)

Eligibility

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

Inclusion criteria

* American Society of Anesthesiologists (ASA) physical status II

Exclusion criteria

* Any known allergy to the studied drugs. * congenital heart disease * Any cardiac problems. * Use of psychotropic medication * mental retardation * any organ dysfunction

Design outcomes

Primary

MeasureTime frameDescription
Postoperative painfor 60 minutes later admission to the post-anaesthesia care unitPostoperative pain will be assessed by the CHEOP scale (Children's Hospital of Eastern Ontario Pain Scale)The scale includes six entries with an appropriate point evaluation focused on the character of crying (1-3 points), facial expressions (0-2 points), verbal reaction (0-2 points), position of the body (1-2 points), touch (1-2 points), and position of the legs (1-2 points). Minimum score is 4 (no pain) and maximum is 13 (maximum pain). Grades are summed together. CHEOPS has a minimum possible score of 4 points (no pain) to a maximum of 13 points (the worst pain). When the postoperative pain score exceeded four, rescue analgesia was given with a 20mg/kg paracetamol suppository.

Secondary

MeasureTime frameDescription
systolic blood pressureat the baseline (after the induction of anesthesia and before administration of the drugs) then every 5min up to 20 minutessystolic blood pressure (mmHg) using sphygmomanometer cuff
The time to the first demand for rescue analgesicduring first 24 hours postoperativeThe time to the first demand for rescue analgesic (minutes or hours)
total number of children who required postoperative pain medicationfor 24 hours after surgery
Heart rateat the baseline (after the induction of anesthesia and before administration of the drugs) then every 5min up to 20 minutesHeart rate (beat/minute) using ECG monitoring
nausea, vomitingduring first 24 hours postoperativeNumber of attacks of nausea and/or vomiting
respiratory difficultyduring first 24 hours postoperativesigns of respiratory difficulty: 1. Breathing rate. An increase in the number of breaths per minute (\>35 breath/minute) 2. Increased heart rate. 3. Color changes. A bluish color seen around the mouth, on the inside of the lips, or on the fingernails 4. Grunting. A grunting sound can be heard each time the person exhales. 5. Nose flaring. The openings of the nose spreading open while breathing 6. Retractions. The chest appears to sink in just below the neck and/or under the breastbone with each breath- 7. Sweating. There may be increased sweat on the head, but the skin does not feel warm to
emergence behaviorevery 5 minutes during first 30 minutes of recovery-emergence behavior will be measured using Aono's four point scale : (1) Asleep; (2) Awake but calm; (3) Agitated but consolable; and (4) Severely agitated and difficult to console and the highest-recorded value was recorded during the Post anesthesia care unit stay. Lowest score is 1 and highest score is 4 The higher score indicates more emergence agitation. For purposes of analysis, grades 1 and 2 in the scale of behavior were considered no agitation and grades 3 and 4 were considered the presence of agitation.

Countries

Egypt

Outcome results

None listed

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