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NCT Number: NCT07538284

MInimizing Delirium With Nasal Dexmedetomidine-InducEd Sleep (MIDDIES)

This study aims to determine whether, compared with placebo, the nighttime self-administration of a nasal dexmedetomidine is effective at inducing sleep and preventing postoperative delirium in high-risk patients.

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Key information

About this study

Delirium is an acute, short-term brain dysfunction characterized by fluctuating consciousness, cognitive decline, inattention, and sleep-wake cycle disruption. Postoperative delirium (POD), occurring predominantly within the first postoperative week (especially days 3-5 in elderly patients), affects 11-45% of older adults after major surgery. POD prolongs hospitalization, increases morbidity and mortality 5,65,6, yet its pathophysiology remains unclear, and evidence-based pharmacological prevention is lacking. Thus, effective POD prevention strategies are urgently needed.

Preoperative anxiety, a modifiable risk factor for POD, affects 11-80% of surgical patients. It contributes to sleep disturbances (e.g., insomnia, early awakening), which may exacerbate POD via neuroendocrine and immune dysregulation. However, benzodiazepines (e.g., lorazepam, diazepam, midazolam), though effective anxiolytics, increase delirium risk and are contraindicated preoperatively per current guidelines.

Dexmedetomidine (DEX), a selective α2-adrenoceptor agonist, induces physiological non-REM sleep without respiratory depression or hemodynamic instability. Its nasal formulation offers high bioavailability (82%), ease of administration, and is approved in China for preoperative sedation/anxiety. While intravenous (IV) DEX reduces POD in predominant ICU settings, its use in general wards remains unexplored. Preclinical studies suggest DEX enhances glymphatic clearance and exerts anti-inflammatory effects, potentially mitigating the development of POD. This study thus hypothesize that a nasal dexmedetomidine is effective at inducing sleep and preventing postoperative delirium in high-risk patient population. We set to demonstrate that to determine whether, compared with placebo, the nighttime self-administration of a nasal dexmedetomidine is effective at inducing sleep and preventing postoperative delirium in older patients undergoing major abdominal surgery.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 65-90 years
  • Scheduled for a major abdominal surgery with estimated surgery time ≥ 2 hours

Exclusion criteria

  • Blind, deafness or the inability to speak mandarin
  • Allergy to dexmedetomidine.
  • Renal and liver failure requiring dialysis or Child-Pugh score > 5
  • Follow-up difficulties (i.e. active substance abuse, psychotic disorder, homelessness)
  • Previous major abdominal or cardiac surgery within 1 year of surgical procedure
  • Chronic therapy with benzodiazepines and/or antipsychotics. Severe deficit due to structural or anoxic brain damage
  • Body weight < 35 kg

Treatment and study plan

Dexmedetomidine

Drug

Intranasal dexmedetomidine (100 µg total: 4 sprays, 25 µg/spray; Hengrui Medicine, China) self-administered preoperatively (~9 PM) and optionally on the night of surgery (patient decides dose: 0, 2 sprays, or 4 sprays).

Placebo

Drug

Intranasal water for injection (4 sprays, identical volume as nasal dexmedetomidine; Hengrui Medicine, China) self-administered preoperatively (~9 PM) and optionally on the night of surgery (patient decides dose: 0, 2 sprays, or 4 sprays).

Primary outcomes

  1. Incidence of postoperative delirium

    Time frame: Up to postoperative day (POD) 7 or discharge (whichever first).

    Confusion Assessment Method

Secondary outcomes

  1. Delirium severity

    Time frame: Up to postoperative day (POD) 7 or discharge (whichever first)

    Confusion Assessment Method Score

  2. Physical activity

    Time frame: Up to postoperative day (POD) 3

    Fitbit Flex2 tracker

  3. Sleep quality

    Time frame: Up to postoperative day (POD) 3

    Fitbit Flex2 tracker and Athens Insomnia Scale

  4. Anxiety

    Time frame: Up to postoperative day (POD) 3

    Hamilton Anxiety Scale

  5. Pain intensity

    Time frame: Up to postoperative day (POD) 3

    Numerical Rating Scale

  6. Opioid consumption

    Time frame: Up to postoperative day (POD) 3

    Intravenous morphine equivalents

  7. Health related quality of life

    Time frame: On postoperative day (POD) 3 and 30

    Health related quality of life assessed with the SF-36 health survey

  8. Quality of Recovery

    Time frame: Up to postoperative day (POD) 3

    The Quality of Recovery-15 questionnaire

  9. Postoperative Nausea and Vomiting

    Time frame: Up to postoperative day (POD) 3

    Postoperative Nausea and Vomiting Scale

  10. Post-anesthesia Care Unit (PACU) length of stay

    Time frame: Up to postoperative day (POD) 1

    Post-anesthesia Care Unit (PACU) length of stay

Other outcomes

  1. Optional intranasal administration on the night of surgery

    Time frame: At night of the surgery

    Optional intranasal administration of the same spray (patient decides dose: 0, 2 sprays, or 4 sprays)

  2. Length of Hospital Stay

    Time frame: From postoperative day 0 until date of hospital discharge (Up to 30 days)

    Medical Record Review

  3. Cognitive function

    Time frame: Up to postoperative day (POD) 30

    Abbreviated Mental Test Score

Study contacts

Contact information is provided by the study sponsor or research team.

Mentying Ding, MD.

CONTACT

[email protected]

+86-15170375679

Sponsors and collaborators

Lead sponsor

Sixth Affiliated Hospital, Sun Yat-sen University

Other

Registry information

Official study title

Minimizing Delirium With Nasal Dexmedetomidine-Induced Sleep in Older Patients Undergoing Major Abdominal Surgery: : a Randomized, Double-blind, Placebo-controlled Trial

Acronym: MIDDIES

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Apr 20, 2026
Registry last updated
Apr 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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