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The Management of Postoperative Craniotomy Pain in Pediatric Patients

NCT01576601 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 81

Last updated 2017-12-11

No results posted yet for this study

Summary

The purpose of this prospective, clinical observational trial is to assess the incidence of pain (and analgesia), methods of pain assessment (and by whom), prescribed analgesics, methods of analgesic delivery, and patient/parent satisfaction in patients undergoing craniotomy surgery at three major children's hospitals (Boston Children's Hospital, Children's Hospital of Philadelphia, The Children's Center Johns Hopkins Hospital) in the United States.

Conditions

  • Post Craniotomy Surgery
  • Cancer
  • Epilepsy
  • Vascular Malformations
  • Craniofacial Reconstructive Surgery

Sponsors & Collaborators

Eligibility

Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-08-31
Primary Completion
2013-06-30
Completion
2013-06-30

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01576601 on ClinicalTrials.gov