Sleep Disorders Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have a partial tear of a specific shoulder tendon (the supraspinatus), where the tear is smaller than 1 cm and affects less than half the tendon's thickness, confirmed by an ultrasound scan
- People whose shoulder pain has been disrupting their sleep for at least 1 month, with a sleep quality score above 5 on a standard sleep questionnaire (called the PSQI)
- People whose shoulder pain is specifically affecting the quality of their sleep
- People with a body mass index (a measure of body weight relative to height) below 30
- People aged between 40 and 75 years
Who may not be able to join:
- People who have other sources of pain alongside their shoulder pain
- People who have previously had surgery on their shoulder
- People who have a psychiatric or neurological condition
- People who have other health conditions known to affect sleep
- People who have osteoporosis, diabetes, or high cholesterol, as these may affect healing and the risk of the injury getting worse
- People who have alcohol dependence, nicotine addiction, or are regularly exposed to second-hand smoke
- People currently taking certain antibiotics (fluoroquinolones), medications that affect sleep (such as melatonin, trazodone, or zolpidem), antidepressants, antipsychotics, or anti-anxiety medications
- People who are unable or unwilling to give consent, are unable to cooperate, or have difficulty with verbal communication
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Michał Kanak, MD, Medical University of Lodz
Phone: 178-334-0150
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Constant-Murley Score; Numeric pain Rating Scale; Range of motion measurements; Strength measurements; BDNF and proBDNF Assessment; Pittsburgh Sleep Quality Index
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.