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Pharmacokinetics of Intranasal Ketorolac in Children

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Columbia University

Status and phase

Terminated
Phase 1

Conditions

Evaluating Pharmacokinetics of Intranasal Ketorolac
Pain

Treatments

Drug: Ketorolac

Study type

Interventional

Funder types

Other

Identifiers

NCT02297906
AAAN5404

Details and patient eligibility

About

Ketorolac is a non-steroidal anti-inflammatory drug (NSAID) that is typically given to both adults and children by the intravenous (IV) or intramuscular (IM) route for analgesic purposes. Ketorolac can also be given by the intranasal (IN) route using a mucosal atomization device (MAD). We aim to study the pharmacokinetics of ketorolac when administered by the IN route using the MAD.

Full description

The intranasal (IN) route of administering medications is an effective means of delivering analgesics to children in a painless and minimally distressing manner, especially in comparison to traditional means of intravenous (IV) or intramuscular (IM) administration, which require a painful and distressing needle stick.

Ketorolac is an analgesic that is commonly administered to children, and can be given by the IN route, in addition to the IV and IM routes. However, the pharmacokinetics of intranasal ketorolac when administered in children has only been described in a limited fashion. The administration of IN ketorolac in children, using the proprietary SPRIX device, which atomizes a fixed amount of ketorolac, produces serum concentrations of ketorolac that are associated with analgesia. However, the concentrations of ketorolac achieved using a mucosal atomization device (MAD) has not yet been evaluated in children presenting to the emergency department. The MAD is a plastic device that attaches to the top of a syringe (see figure). The MAD is much more commonly used for atomizing medications; allows a variable dosage to be administered; and has been shown to be a means of effectively delivering other analgesics and sedatives intranasally.

The purpose of this study is to assess the pharmacokinetics of IN ketorolac when using a MAD to deliver the medication in children presenting to the emergency department. We will determine the maximum serum concentration achieved (Cmax), time to maximum serum concentration achieved (Tmax), and bioavailability (compared to IV ketorolac) when ketorolac is administered intranasally using a MAD.

Enrollment

18 estimated patients

Sex

All

Ages

8 to 17 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Present to the emergency department with a painful condition for which the treating physician decides to administer ketorolac as part of their usual care.

Exclusion criteria

  • Known allergy to ketorolac
  • Contraindication to receiving ketorolac
  • Receiving any NSAID within the past 6 hours
  • Presence of an intranasal obstruction that cannot be readily cleared using suction or nose-blowing
  • Inability to speak English or Spanish
  • Critical illness

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

18 participants in 2 patient groups

Intranasal ketorolac
Experimental group
Description:
Ketorolac 0.5 mg/kg, maximum single dose = 30 mg. Administered once by intranasal route using a mucosal atomization device.
Treatment:
Drug: Ketorolac
Intravenous ketorolac
Active Comparator group
Description:
Ketorolac 0.5 mg/kg, maximum single dose = 30 mg. Administered once by intravenous route.
Treatment:
Drug: Ketorolac

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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