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NCT03744520

Sensorial Block Assessment of Erector Spinae Block

Completed NA Last updated 4 October 2019
What this trial tests

NA trial testing Erector spinae plane block in Regional Anesthesia Morbidity in 50 participants. Completed in 3 October 2019.

Timeline
15 November 2018
Primary endpoint
3 October 2019
3 October 2019

Quick facts

Lead sponsorOnur Selvi
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposescreening
Enrollment50
Start date15 November 2018
Primary completion3 October 2019
Estimated completion3 October 2019
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Onur Selvi

Who can join

18 and older, any sex, with Regional Anesthesia Morbidity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Ultrasound-guided erector spinae plane blocks are used as postoperative analgesia method for abdominal, chest and hip surgeries. Regional techniques are well-described methods for postoperative analgesia. However, the sensorial dermatomal spread of regional block varies depending on the multiple variables as the level of the block, local analgesic concentration etc. The aim of this study is to observe dermatomal evaluation of sensorial block.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Erector spinae plane block

Trials testing the same drug.

Other recruiting trials for Regional Anesthesia Morbidity

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03744520.

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