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RECRUITING
NCT06557044
NA

The Analgesic Efficacy of Pericapsular Nerve Group (PENG) Block in Patients Undergoing Primary Total Hip Arthoplasty:

Sponsor: Diakonie-Klinikum Stuttgart

View on ClinicalTrials.gov

Summary

The aim of this study is to investigate the analgesic efficacy of the pericapsular nerve group (PENG) block during the implantation of hip endoprostheses. The study is designed as a prospective randomized double-blind study and the study participants were randomized into 2 arms and either 20 ml ropivacaine 0.5% (verum group) or 20 ml physiological saline solution (placebo group) will be applied.

Official title: The Analgesic Efficacy of Pericapsular Nerve Group (PENG) Block in Patients Undergoing Primary Total Hip Arthoplasty: a Prospective, Double-blinded, Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

110

Start Date

2024-03-07

Completion Date

2025-03

Last Updated

2024-08-16

Healthy Volunteers

No

Interventions

DRUG

Ropivacaine

PENG block with ropivacaine

OTHER

Physiological saline

Placebo control

Locations (1)

Diakonie-Klinikum Stuttgart

Stuttgart, Baden-Wurttemberg, Germany