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NCT04133467

Scalp Block Decreases Pain and Side Effects

Completed Last updated 22 October 2019
What this trial tests

trial testing scalp block in Craniosynostoses in 26 participants. Completed in 30 June 2016.

Timeline
1 January 2016
Primary endpoint
30 June 2016
30 June 2016

Quick facts

Lead sponsorFondazione Policlinico Universitario Agostino Gemelli IRCCS
StatusCompleted
Study typeOBSERVATIONAL
Enrollment26
Start date1 January 2016
Primary completion30 June 2016
Estimated completion30 June 2016
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Who can join

Adults 3 Months to 2, any sex, with Craniosynostoses or Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The scalp block for postoperative pain control in craniosynostosis surgery: a case control study.
    Festa R, Tosi F, Pusateri A, Mensi S, et al · · 2020 · cited 9× · PMID 32418049 · DOI 10.1007/s00381-020-04661-z

Verify or expand the search:

Other trials of scalp block

Trials testing the same drug.

Other recruiting trials for Craniosynostoses

Currently open trials in the same condition.

Other Fondazione Policlinico Universitario Agostino Gemelli IRCCS trials

Trials by the same sponsor.

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Data sources for this page

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