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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05341154
Other study ID # 548 / 7 / 2021
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2021
Est. completion date May 6, 2023

Study information

Verified date May 2023
Source Aswan University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Delirium is a common postoperative complication in the elderly, often caused by multiple factors. It is defined as an acute neuropsychiatric disorder characterized by fluctuating disturbances in attention, awareness, and cognition. Postoperative delirium occurs in 17-61% of the major surgical procedures. It may be associated with cognitive decline, decreased functional independence, increased risk of dementia, caregiver burden, health care costs, morbidity, and mortality. Therefore, delirium is a possibly disastrous condition and is both a huge burden on a patient's health and on the health care system in general.


Description:

Over the last few decades, numerous risk factors for delirium have been identified, emphasizing the importance of delirium prevention in patients undergoing surgery. It has already been identified as a state that may be associated with serious complications such as prolonged ICU and hospital stays, decreased quality of life, and increased mortality ). Previous studies on delirium pointed out old age and other factors as important predisposing factors. on the health care system in general. Extensive research on reducing the incidence of delirium has been conducted using both pharmacological and non-pharmacological preventive measures in the acute setting. As evidence recommending or opposing specific drugs for the prevention of postoperative delirium remains insufficient and the international guidelines can only recommend perioperative pharmacologic adjustments ("American Geriatrics Society Abstracted Clinical Practice Guideline for Postoperative Delirium in Older Adults," 2015) . Consequently, the challenge of developing reliable hospital algorithms for delirium prevention and treatment remains unresolved. Furthermore, there is a link between postoperative delirium and two biomarkers, cortisol and C- Reactive Protein (CRP), which have previously been linked to delirium but whose significance is unknown.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 6, 2023
Est. primary completion date May 6, 2023
Accepts healthy volunteers No
Gender All
Age group 60 Years to 80 Years
Eligibility Inclusion Criteria: - 1- Patients aged = 65 years. 2- Scheduled for visceral, orthopedic, vascular, obstetric, urology, or plastic surgery. Exclusion Criteria: - 1- Delirium upon hospital admission or development of delirium prior to surgery stated by family members. 2- Mini-Mental State Examination (MMSE) score < 24 points 3- Delirium Observation Scale (DOS) =4 points 4- preoperative neurological diseases affecting cognitive function (such as vascular dementia) 5- High risk for postoperative treatment in the intensive care unit (ICU) 6- Known to have dexmedetomidine and or ketamine intolerance. 7- Lack of cooperation or communication. 8- Parkinson's disease, parkinsonism, intake of dopaminergic drugs (levodopa, dopamine agonists) 9- Epilepsy. 10- Patients on steroid therapy 11- severe liver and renal insufficiency

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ketamine Hcl 50Mg/Ml Inj
Patients will be given the active comparator or placebo only once right before the induction of anesthesia.

Locations

Country Name City State
Egypt Huda Fahmy Mahmoud Aswan

Sponsors (1)

Lead Sponsor Collaborator
Huda Fahmy Mahmoud, PhD

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative cognitive impairment by Mini Mental State Examination (MMSE) score Mini Mental State Examination (MMSE) score < 24 points 72 hours
Primary Postoperative delirium by Delirium Observation Screening Scale (DOS) >4 points 72 hours
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