Low-Dose Ketamine Infusion for Children With Sickle Cell Disease-Related Pain

Sickle Cell Disease Clinical Trial

Official title: Use of Low-Dose Ketamine Infusion in Acute Painful Episodes of Sickle Cell Disease: A Pilot Study

Status Terminated

Clinical Trial Summary

Acute pain episodes associated with sickle cell disease (SCD) are very difficult to manage effectively. Opioid tolerance and side effects have been major roadblocks in our ability to provide these patients with adequate pain relief. This pilot study is designed to examine the safety and feasibility of using ketamine, an N-methyl-D-aspartate (NMDA) receptor antagonist, in the inpatient seeing with children and adolescents who have sickle cell vasoocclusive pain. Previous research suggests that in subanesthetic doses, ketamine may be able to prevent the development of opiate tolerance and facilitate better pain relief with lower opiate doses, allowing for less respiratory depression, less sedation, easier ambulation, less deconditioning, shorter hospital stays, and better quality of life. The goal of this pilot study is to evaluate the safety and feasibility of using a continuous infusion of ketamine, in conjunction with opiates, in the inpatient setting for sickle cell vasoocclusive pain. It is hypothesized that using a low dose ketamine infusion in conjunction with opiates will be a safe and feasible practice for the treatment of sickle cell pain.

Clinical Trial Description

3.2 Study Design/Type

1. Patient meeting inclusion/exclusion criteria is enrolled up to 24 hours after admission for a vasoocclusive episode.

2. Prior to onset of ketamine infusion, the following information is collected:

1. Demographic information (age, gender, SCD genotype, past history of SCD-related complications) [Obtained from the patient's medical chart]

2. Opiate utilization/hour since admission [Obtained from the patient's medical chart]

3. Numerical Rating Scale (NRS) scores since admission [Obtained from the patient's medical chart]

4. Sedation score (University of Michigan Sedation Scale) is obtained [By the nursing staff]

5. Body outline figure of the Adolescent Pediatric Pain Tool (validated down to age 7) is administered [By the research staff]

6. Ketamine Effects Scale (KES) is administered to the patient [By the research staff]

3. Ketamine infusion is begun at 0.05 mg/kg/hour.

4. After infusion is initiated:

1. Vital signs are taken every hour for two hours after infusion begins, then after two hours, then every four hours for the remainder of the hospitalization [Completed by the nursing staff]

2. Pain scores are recorded with vital signs if the patient is awake [Completed by nursing staff]

3. Patient is also asked if pain is a lot better, a little better, no change, a little worse, or a lot worse than previous assessment [Completed by nursing staff]

4. Sedation score (University of Michigan Sedation Scale) assessed with pain score [Completed by the nursing staff]

5. Adolescent Pediatric Pain Tool (APPT) body outline figure is completed by the patient once per day between 3 pm and 5 pm. [Administered by the research staff]

6. Ketamine Effects Scale (KES) is administered to the patient once per day between 3pm and 5pm [By the research staff]

7. Patient is monitored for side effects including dreams, disorientation, dysphoria, agitation, CNS depression, respiratory depression, increasing hypoxia, nausea, or vomiting [Completed by the nursing or research staff]

8. Need for supplemental oxygen is recorded (oxygen saturation <95%) [Completed by nursing staff]

9. Opiate use and NSAID use/6 hours is recorded [Completed by the nursing or research staff]

5. The infusion may be discontinued or decreased at any time due to unacceptable side effects as determined by the clinician, patient, parent, or principal investigator.

6. Agents designed to reduce ketamine side effects [midazolam (Versed), clonidine, lorazepam (Ativan), or diazepam (Valium)] may be administered at the discretion of the attending physician or the principal investigator.

7. 4 hours or more after infusion begins, the infusion rate may be increased to 0.1 mg/kg/hour if the following parameters are met:

1. patient's pain has not improved to an acceptable range (pain score is still ≥5)

2. side effects remain acceptable

8. 4 hours or more after the previous increase the ketamine infusion may be increased to 0.15 mg/kg/hour per parameters.

9. 4 hours of more after the previous increase the ketamine infusion may be increased to 0.2 mg/kg/hour per parameters.

10. The ketamine infusion will be discontinued at the time of transition to oral pain medication, or no more than 72 hours after initiation, or at the request of the clinician, patient, parent, or principal investigator.

11. Pain scores, vital signs, sedation score, opiate use, APPT body outline figure, and KES score will be recorded as above for the remainder of the hospitalization.

12. Total length of hospitalization will be recorded.

13. Patient will be contacted on a weekly basis for 4 weeks following hospitalization for review of potential side effects, pain episodes, or events leading to re-admission.

14. The patient's medical record will be reviewed to determine duration of previous hospitalizations for SCD pain in the previous 24 months and opiate utilization, pain scores, and transition to oral opiates during those hospitalizations.

3.3 Randomization

This will be conducted as a pilot study; patients will not be randomized.

3.4 Duration

The length of the patient's participation in this study is the duration of their hospitalization, as well as 4 weeks worth of follow-up phone calls.

3.5 Discontinuation

Individual patients will stop receiving ketamine if they develop acute chest syndrome (ACS), have a stroke, are transferred to the Intensive Care Unit (ICU), if their hemoglobin falls below 5 mg/dl, if they experience unacceptable side effects, or at the request of the PI, attending, patient, or parent. However, they will continue to be in the study and all data will be collected throughout the duration of their hospitalization.

The entire trial will be terminated when 20 patients have completed the protocol, or if there is an unexpected rate of acute chest syndrome or admissions to the pediatric intensive care unit (PICU). ;

Related Conditions & MeSH terms

• Anemia, Sickle Cell
• Sickle Cell Disease

• NCT number: NCT00595530
• Study type: Interventional
• Source: Connecticut Children's Medical Center
• Status: Terminated
• Phase: Phase 2
• Start date: March 4, 2008
• Completion date: February 12, 2010