CompletedPhase 2ketamine

Comparison of the Efficacy of Ketamine in Pediatric Patients With Idiopathic Scoliosis After Surgery

Sponsored by Fundació Sant Joan de Déu

NCT ID
NCT02571491
Target Enrollment
48 participants
Start Date
2012-01
Est. Completion
2014-02

About This Study

Comparison of the Efficacy of ketamine measuring the total consumption of morphine in pediatric patients with idiopathic scoliosis

Conditions Studied

Progressive Infantile Idiopathic Scoliosis

Interventions

  • Ketamine Hydrochloride
  • Placebo
  • Remifentanil
  • Morphine hydrochloride

Eligibility

Age:8 Years - 18 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

1. Patients of both genders diagnosed with idiopathic scoliosis aged between 8 and 18 years old.
2. Patients of both genders diagnosed with idiopathic scoliosis and candidates for vertebral fusion corrective surgery with instrumentation.
3. Patients with ASA 1 or ASA 2.
4. Patients and/or parents/tutors consent to participate in the clinical trial.

Exclusion Criteria:

1. Patients with chronic preoperative pain.
2. Patients with addiction to narcotics.
3. Patients with a history of allergy, contraindication or intolerance to the drugs used.
4. Patients unable to understand the patient-controlled analgesia system.
5. Patients with mental disorders.
6. Reoperated patients.
7. Patients requiring elective postoperative ventilation.
8. Pregnant patients.

Study Locations (1)

Hospital Sant Joan de Déu
Esplugues de Llobregat, Barcelona, Spain

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

Find recruiting trials
Data Source
ClinicalTrials.gov

Last updated from source