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Scalp Block Decreases Pain and Side Effects

NCT04133467 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 26

Last updated 2019-10-22

No results posted yet for this study

Summary

Postoperative analgesia after corrective surgery of paediatric craniosynostosis is crucial in term of short and long-term outcomes. The objective of this observational case- control study was to evaluate the effectiveness of an analgesic technique based on the scalp block versus traditional pharmacological approach.

Conditions

  • Craniosynostoses
  • Pain, Postoperative

Interventions

OTHER

scalp block

intravenous acetaminophen according to the body weight, plus intravenous tramadol 1 mg/kg)

Sponsors & Collaborators

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

    lead OTHER

Principal Investigators

  • Rossano festa, MD · Fondazione Universitaria Policlinico Gemelli IRCCS roma Italia

Eligibility

Min Age
3 Months
Max Age
2 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-01
Primary Completion
2016-06-30
Completion
2016-06-30

Countries

  • Italy

Study Locations

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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 NCT04133467 on ClinicalTrials.gov