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NCT04692857

US-guided FICB After Hip Fracture: the Effect of the Local Anesthetic Volume on the Quality of Preoperative Analgesia

Completed NA Last updated 5 January 2021
What this trial tests

NA trial testing supra inguinal fascia iliaca block in Hip Fractures in 75 participants. Completed in 31 August 2020.

Timeline
2 January 2020
Primary endpoint
31 August 2020
31 August 2020

Quick facts

Lead sponsorUniversity Tunis El Manar
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposebasic science
Enrollment75
Start date2 January 2020
Primary completion31 August 2020
Estimated completion31 August 2020
Sites1 location across Tunisia

Drugs / interventions tested

Conditions studied

Sponsor

University Tunis El Manar

Who can join

65 and older, any sex, with Hip Fractures. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

participants were randomly divided into three groups : group 30 , group 40 and group 50 . for all the three groups an ultrasound guided supra-inguinal fascia iliaca block had been performed. for group 30 ,a volume of 30 ml of 0,2 % ropivacaine had been injected for group 40 ,a volume of 40 ml of 0,2 % ropivacaine had been injected for group 50 ,a volume of 50 ml of 0,2 % ropivacaine had been injected

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 recruiting trials for Hip Fractures

Currently open trials in the same condition.

Other University Tunis El Manar trials

Trials by the same sponsor.

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/NCT04692857.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing