NCT06527105 Impact of Sleep Quality on Outcomes After Cardiac Surgery
| NCT ID | NCT06527105 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Amrita Institute of Medical Sciences & Research Center |
| Condition | Sleep |
| Study Type | INTERVENTIONAL |
| Enrollment | 100 participants |
| Start Date | 2024-07-22 |
| Primary Completion | 2024-12-31 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 100 participants in total. It began in 2024-07-22 with a primary completion date of 2024-12-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Sleep is a basic human need and is essential for good quality of life, good health. In fact, humans spend one third of their life time in sleeping or attempting to do so. However, sleep is not given due importance in intensive care unit (ICU)'s, although it is critical in healing process. Patient's usually get admitted to the hospital few days prior to the surgery, for complete evaluation, depending on the procedure planned. Hospital environment being, an entirely new place for inpatients, will invariably affect their sleep. Sleep deprivation is one of the major sources of anxiety and stress in all the patients during ICU stay. This means that most of patients are sleep deprived, by the time they are admitted to ICU. The negative effects of sleep deprivation include postoperative brain dysfunction like inattention, restlessness, hallucinations, agitation, aggressiveness. The degree of cognitive impairment may range from subtle derangements in attention, reason, clarity of thought and capacity of decision making to confusion and delirium. Sleep deprivation can also induce hypertension, fatigue, metabolic disorders, cerebrovascular and cardiovascular disease
Eligibility Criteria
Inclusion Criteria: * Adult cardiac surgical patients aged above 18years undergoing elective cardiac surgery Exclusion Criteria: * Not willing to give consent * Preoperative sleep medications use * Preoperative psychological disorders, on mechanical ventilation for \>12hrs, dementia, cerebrovascular accident
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06527105 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Sleep. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06527105 currently recruiting?
Yes, NCT06527105 is actively recruiting participants. Contact the research team at drarjun83@gmail.com for enrollment information.
Where is the NCT06527105 trial being conducted?
This trial is being conducted at Kochi, India.
Who is sponsoring the NCT06527105 clinical trial?
NCT06527105 is sponsored by Amrita Institute of Medical Sciences & Research Center. The trial plans to enroll 100 participants.