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NCT05921110: PENG

Evaluation of the Effectiviness of Two Different Bupivacaine Concentrations of the Pericapsular Nerve Group (PENG) Block

Status unknown NA Last updated 27 June 2023
What this trial tests

NA trial testing Pericapsular nerve group block 0,25% in Hip Fractures in 66 participants. Status unknown.

Timeline
15 May 2023
Primary endpoint
30 November 2023
30 November 2023

Quick facts

Lead sponsorIlker Ital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment66
Start date15 May 2023
Primary completion30 November 2023
Estimated completion30 November 2023
Sites2 locations across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Ilker Ital

Who can join

Adults 18 to 85, any sex, with Hip Fractures or Postoperative Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The use of regional anaesthesia techniques as part of multimodal analgesia in hip surgeries improves postoperative analgesia. PENG (Pericapsular nerve group) block is an effective motor sparing analgesia technique used in hip surgeries. The purpose of this study was to assess the efficacy of PENG block in terms of analgesic requirements and pain density in patients undergoing hip surgery, using two different concentrations of local anaesthetic.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hip Fractures

Currently open trials in the same condition.

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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/NCT05921110.

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