Hypnotics And Sedatives

3

Review clinical trials related to Hypnotics And Sedatives. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Nebulized Ketamine for the Treatment of Major Depressive Disorder

This is a double-blind active placebo controlled clinical trial for individuals with moderate to severe depression. The purpose of this study is to assess if nebulized ketamine can reduce depressive symptoms.

Participants needed: 40
Trial details
Phase: Phase 3Age: 18-88Biological sex: AllType: InterventionalSponsor: Theresa Jacob, PhD, MPHUpdated: Apr 24, 2026Locations: 1
Eligibility criteria

All individuals 18 years and older with a Montgomery-Asberg Depression Rating Sc... [+2]

Adult patients with an allergy to Ketamine [+14]

Status: Recruiting

Cognitive Outcomes After Dexmedetomidine Sedation in Cardiac Surgery Patients

Anesthesia is a drug induced, reversible, comatose state that facilitates surgery and it is widely assumed that cognition returns to baseline after anesthetics have been eliminated. However, many patients have persistent memory impairment for weeks to months after surgery. Cardiac surgery appears to carry the highest risk of postoperative cognitive dysfunction (POCD). These cognitive deficits are associated with increased mortality, prolonged hospital stay and loss of independence. The investigators propose to investigate the role of Dexmedetomidine (DEX) in preventing long-term POCD after cardiac surgery and enhancing early postoperative recovery. It is anticipated that DEX will be the first effective preventative therapy for POCD, improve patient outcomes, and reduce length of stay and healthcare costs.

Participants needed: 2,400
Trial details
Phase: Phase 4Age: 60+Biological sex: AllType: InterventionalSponsor: Sunnybrook Health Sciences CentreUpdated: Dec 1, 2025Locations: 8
Eligibility criteria

Planned CABG (+/- valve, including off-pump) or valve replacement via sternotomy... [+1]

Lack of patient consent [+4]

Status: Recruiting

Patient-centred Deprescribing of Psychotropic, Sedative and Anticholinergic Medication in Elderly Patients With Polypharmacy

The PARTNER study is a multicentre, two-arm, pragmatic cluster-randomised trial evaluating the impact of a focused and patient-centred cooperation between general practitioners (GPs) and community pharmacists (PARTNER intervention) on reductions in the use of psychotropic, sedative and anticholinergic potentially inappropriate medication (PSA-PIM) compared to a control intervention. The PARTNER intervention comprises (1) education for health care professionals, (2) an interprofessional workshop and case conference, (3) a pharmacy visit with brown bag/medication review and patient empowerment, (4) GP practice visit with shared decision making. The control intervention only comprises a pharmacy visit with brown bag review.

Participants needed: 352
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Ludwig-Maximilians - University of MunichUpdated: May 4, 2025Locations: 3
Eligibility criteria

Aged 65 years or older [+5]

Terminal illness (life expectancy < 6 months) [+5]