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Study identifier: NCT07658326 Synced from ClinicalTrials.gov · July 29, 2026
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Preoperative Stress Assessment in Patients Undergoing Surgery for Rotator Cuff Tendinopathy

Condition: Stress · Tendinopathy Rotator Cuff  ·  Sponsor: GCS Ramsay Santé pour l'Enseignement et la Recherche

PhaseN/A
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Orthopedic surgery of the limbs presents a unpredictable postoperative course, which can be more or less lengthy in terms of functional recovery and resumption of personal or professional activities. Not uncommon, convalescence can require many months with dramatic personal and/or socio-professional consequences (disability, unemployment, etc.), particularly in the postoperative development of complex regional pain syndrome (CRPS) and/or adhesive capsulitis. Among the suspected contributing factors, the existence of an unfavorable preoperative psychological context in patients is often mentioned. This research is based on the hypothesis that a high level of preoperative stress in patients could contribute to the occurrence of more significant postoperative complications in patients who have undergone shoulder surgery. The main objective is to measure the level of preoperative stress in patients undergoing surgery for rotator cuff tendinopathy.

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

Talk to the study team

Jean-François Oudet  ·  0033683346567  ·  jf.oudet@ecten.eu

Marie-Hélène Barba  ·  mh.barba@ecten.eu

Always discuss trial participation with your own doctor first.

Locations (3)

Clinique des CèdresCornebarrieu, FranceRecruiting
Clinique la croix du sudQuint-Fonsegrives, FranceRecruiting
Clinique de l'UnionSaint-Jean, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07658326