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:
- Adults aged 18 or older (both men and women)
- People whose blood pressure is higher than normal during sleep (specifically, an average sleeping systolic blood pressure of 120 mmHg or more), measured at the time they are enrolled
- People who follow a regular routine of being active during the day and sleeping at night
- People who are willing to sign a form giving their consent to take part in the study
Who may not be able to join:
- People who are pregnant
- People who have had a problem with drug or alcohol misuse in the last two years
- People who work night shifts or rotating shift schedules
- People who have been diagnosed with a systemic autoimmune disease or AIDS
- People whose high blood pressure is caused by a specific underlying medical condition, such as a narrowing of the main heart artery, a hormone-producing tumour, or narrowing of the arteries supplying the kidneys (confirm with trial site)
- People with certain serious heart or circulation conditions, such as unstable chest pain, heart failure, dangerous irregular heartbeat, a specific heart rhythm disorder called atrial fibrillation, kidney failure, or severe eye damage related to blood pressure. Note: people who have had a past heart or circulation event may still be considered, as long as they are able to carry out their normal physical and daily activities
- People with a past or current serious cancer, including blood cancers such as leukaemia or lymphoma, or any other severe life-threatening illness in the last five years (minor skin cancers of the basal cell type are not excluded)
- People who have had surgery or have a medical condition that could affect how the body processes medications, or that the study doctor believes could put them at higher risk or prevent them from completing the study requirements
- People who are unable to communicate clearly or follow the study requirements
- People who are unable to tolerate wearing a 24-hour blood pressure monitoring device (a cuff that measures blood pressure at regular intervals throughout the day and night)
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: Ramon C Hermida, PhD, University of Vigo
Phone: 34986812148
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
Vascular events; New-onset type 2 diabetes; New-onset CKD
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.