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NCT05256056

Volume Dependent Effect of Pericapsular Nerve Block

Completed NA Last updated 3 June 2022
What this trial tests

NA trial testing Bupivacain in Post Operative Pain in 60 participants. Completed in 1 June 2022.

Timeline
25 February 2022
Primary endpoint
1 June 2022
1 June 2022

Quick facts

Lead sponsorSisli Hamidiye Etfal Training and Research Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment60
Start date25 February 2022
Primary completion1 June 2022
Estimated completion1 June 2022
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Sisli Hamidiye Etfal Training and Research Hospital

Who can join

18 and older, any sex, with Post Operative Pain or Femur Fracture. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In PENG block technique, the local anesthetic agent is injected between the psoas tendon and the pubic ramus to block the sensory branches of the nerves which innervates the hip capsule for providing analgesia without causing muscle weakness. Since the PENG block is a facial plane block, it causes a volume dependent distribution. There are a few case reposts and cadaveric studies on volume dependent effect of analgesia and motor weakness of PENG block. In our study, we aimed to evaluate the clinical effects of the volume-dependent efficacy of PENG block.

Publications & conference data

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

Verify or expand the search:

Other trials of Bupivacain

Trials testing the same drug.

Other recruiting trials for Post Operative Pain

Currently open trials in the same condition.

Other Sisli Hamidiye Etfal Training and Research Hospital trials

Trials by the same sponsor.

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Data sources for this page

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