Multimodal Analgesia in Children and Adolescents After the Ravitch Procedure and Thoracotomy

Sponsor
National Institute for Tuberculosis and Lung Diseases, Poland (Other)
Overall Status
Completed
CT.gov ID
NCT03444636
Collaborator
(none)
94
1
2
24.4
3.9

Study Details

Study Description

Brief Summary

The study was performed in patients aged 6-18 years after the Ravitch procedure and thoracotomy. The primary aim of the study was to evaluate the efficacy and safety of pain control provided by the multimodal approach that involves the continuous infusion ropivacaine with fentanyl vs. bupivacaine with fentanyl through thoracic epidural catheter. Secondary aims were to identify the determinants of acute post-operative pain at rest, during deep breathing and coughing.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

The subjects were randomized to the Ropivacaine/Fentanyl (RF) or Bupivacaine/Fentanyl (BF) group.

To perform a thoracic surgical procedure, all patients were premedicated with midazolam, and then, paracetamol, non-steroidal anti-inflammatory drugs, fentanyl, propofol, pancuronium or rocuronium (in children < 10 years old) and suprane were used to introduce and maintain the anesthesia. Thoracic epidural catheters were placed following induction of anesthesia and endotracheal intubation.

Intraoperative analgesia was introduced by a single dose of lidocaine 2% (2 mg/kg). Then after 15 minutes, the patients from the RF group received ropivacaine 1% (1-3 mg/kg) and those from the BF group bupivacaine 0.5% (0.5-1 mg/kg). After 60 minutes 0.2% ropivacaine solution with fentanyl or 0.125% solution of bupivacaine with fentanyl was infused with the flow rate of 0.1 ml/kg/hr.

Depending on the allocation to the group, postoperative analgesia was continued either with 0.2% ropivacaine and fentanyl or 0.125% bupivacaine and fentanyl, based on the concentration and the flow rate described above. In addition, intravenous paracetamol was administered as standard every 6 hours (the maximum of 60 mg/kg daily) along with non steroidal anti-inflammatory drugs. In children > 14 years of age, ketoprofen was injected at the dose of 1 mg/kg (the maximum of 200 mg daily) and in younger children ibuprofen (orally or rectally, up to 30 mg/kg daily) every 8 hours. Metamizol was given as a "rescue drug" (20 mg/kg).

Study Design

Study Type:
Interventional
Actual Enrollment :
94 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Efficacy and Safety of Multimodal Analgesia in Children and Adolescents After the Ravitch Procedure and Thoracotomy - a Prospective Randomized Study
Actual Study Start Date :
Mar 2, 2015
Actual Primary Completion Date :
Mar 14, 2017
Actual Study Completion Date :
Mar 14, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Ropivacaine/Fentanyl

Drug: Ropivacaine/Fentanyl
Ropivacaine 0.2% with Fentanyl 5 µg/ml; flow rate of 0.1 ml/kg/hr
Other Names:
  • ROPIVACAINE HYDROCHLORIDE 10 mg/ml
  • Active Comparator: Bupivacaine/Fentanyl

    Drug: Bupivacaine/Fentanyl
    Bupivacaine 0.125% with Fentanyl 5 µg/ml; flow rate of 0.1 ml/kg/hr
    Other Names:
  • BUPIVACAINE HYDROCHLORIDE 0.5%
  • Outcome Measures

    Primary Outcome Measures

    1. Pain intensity scores at rest (FLACC for patients <7 y.o., Numerical Rating Scale for patients >7 y.o.) [postoperative day: 0-3]

    2. Pain intensity scores during deep breathing (FLACC for patients <7 y.o., Numerical Rating Scale for patients >7 y.o.) [postoperative day: 0-3]

    3. Pain intensity scores during coughing (FLACC for patients <7 y.o., Numerical Rating Scale for patients >7 y.o.) [postoperative day: 0-3]

    4. Side Effect Occurrence [first 3 days after surgery]

    Secondary Outcome Measures

    1. Total fentanyl consumption [µg] [postoperative day: 0-3]

    2. The number of doses of metamizol as a "rescue drug" [postoperative day: 0-3]

    3. The number of nursing interventions undertaken to relive pain > 2/10 pts [postoperative day: 0-3]

    4. Patient satisfaction [postoperative day 3]

      Satisfaction was evaluated on a 4-item scale: analgesia was rated as insufficient, poor, good or very good.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    5 Years to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Elective thoracic surgery (thoracotomy or Ravitch procedure);

    • Analgesia: continuous thoracic epidural analgesia.

    Exclusion Criteria:
    • American Society of Anesthesiologists physical status >III;

    • History of chronic pain or preoperative opioid use;

    • Oncological treatment;

    • Impaired verbal communication;

    • Removal of epidural catheter <24 h postoperatively;

    • Lack of postoperative chest drainage.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Institute for Tuberculosis and Lung Diseases, Pediatric Division Rabka-Zdrój Małopolska Poland 34-700

    Sponsors and Collaborators

    • National Institute for Tuberculosis and Lung Diseases, Poland

    Investigators

    • Study Director: Lucyna Tomaszek, PhD, National Institute for Tuberculosis and Lung Diseases, Poland

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Lucyna Tomaszek, PhD, RN, Director of Nursing, Specialist Nurse in Anesthesia and Intensive Care, National Institute for Tuberculosis and Lung Diseases, Poland
    ClinicalTrials.gov Identifier:
    NCT03444636
    Other Study ID Numbers:
    • 10.7
    First Posted:
    Feb 23, 2018
    Last Update Posted:
    May 28, 2020
    Last Verified:
    May 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Lucyna Tomaszek, PhD, RN, Director of Nursing, Specialist Nurse in Anesthesia and Intensive Care, National Institute for Tuberculosis and Lung Diseases, Poland
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 28, 2020