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Study identifier: NCT07172984 Synced from ClinicalTrials.gov · July 28, 2026
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The Value of Standardized Respiratory Rate Monitoring Exercises During Rheumatological Injection Procedures

Condition: Rheumatological Injection · Pain Management · Respiratory Monitoring  ·  Sponsor: Centre Hospitalier Metropole Savoie

PhaseNA
Planned participants136
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to demonstrate the non-inferiority of standardized breathing control exercises on perceived pain during rheumatological injections procedures compared to standard care consisting of the addition of a local anesthetic. The study population will consist of patients scheduled to undergo therapeutic ultrasound-guided joint or periarticular injection. The main question it aims to answer is: * Non-inferiority of breathing exercises compared to the addition of local anesthetic on pain and anxiety experienced during an infiltration procedure. * Correlation between the reduction in pain and anxiety experienced during a procedure and the cardiac coherence score obtained. Researchers will compare the anesthesia group (Arm A), which will receive local anesthesia with 5 cc of lidocaine before the infiltration procedure to the breathing group (Arm B), which will receive instructions before the injection procedure on how to perform 5-minute breathing cycles to facilitate the achievement of cardiac coherence to see if the pain perceived in Arm B is not greater than the pain perceived in Arm A. Participants will be kept blind to their randomization group. Arm A (anesthesia) will receive SHAM breathing exercises, while Arm B (breathing) will receive a placebo injection of anesthetic.

This description comes directly from the study's public registry record.

Talk to the study team

leo blervaque  ·  +33 4 79 96 58 13  ·  urc@ch-metropole-savoie.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Centre Hospitalier Métropole SavoieChambéry, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07172984