The Effect of Esketamine on Sleep Disturbance (NCT06388824) | Clinical Trial Compass
CompletedNot Applicable
The Effect of Esketamine on Sleep Disturbance
China204 participantsStarted 2024-05-03
Plain-language summary
To explore the efficacy of a single low dose of esketamine during surgical abortion in patients with sleep disturbance
Who can participate
Age range
18 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Patients aged 18 years or older with sleep disturbance;
. American Society of Anesthesiologists physical status I-III;
. A gestational age below 12 weeks;
. Elective surgery is proposed;
. BMI of 19-30 kg/m2;
. Patients who agreed to enroll in this study voluntarily
Exclusion criteria
. Any contraindications to ketamine or esketamine;
. Allergic history of general anesthesia drugs, opioid drugs, non-steroidal drugs;
. Respiratory insufficiency, respiratory failure;
. Bronchial asthma, severe hypertension, severe hepatic and renal dysfunction, severe cardiovascular disease, or hyperthyroidism;
. BMI\<18 kg/m2 or BMI\>30kg/m2;
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
The incidence of sleep disturbance on the first night after surgery
Timeframe: the first night after surgery
Trial details
NCT IDNCT06388824
SponsorTianjin Medical University General Hospital
. Poor compliance, unable to complete the experiment according to the study plan; Participants who have participated in clinical trials of other drugs within the last 4 weeks;
. Any circumstances deemed unsuitable for inclusion by the researcher for any reason.