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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05236907
Other study ID # Melatonin123
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date November 1, 2020

Study information

Verified date February 2022
Source University of Baghdad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Postoperative delirium is a complication that should not be underestimated. As it elaborates many complications that could be avoided when an accurate assessment of the risk factors and interventional measures are taken appropriately when needed.


Description:

Delirium is a variation in concentration capabilities that occurs acutely in association with a disturbed level of consciousness. Delirium is more common in orthopaedic surgery patients than in general surgery patients. As delirium ratios range from 44% to 55% in hip surgery patients, otherwise only 10%-14% of general surgery patients. Several studies were carried out and found that melatonin levels correlate with the development of delirium postoperatively. This study was conducted to determine the efficacy of administering melatonin preoperatively in patients undergoing orthopedic surgery to prevent postoperative delirium.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date November 1, 2020
Est. primary completion date October 30, 2020
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: 1- Patients in good general health. 2. Baseline MDAS <13. 3. No seizure disorder. Exclusion Criteria: 1. Patients with a neurological disorder (e.g., dementia, stroke, epilepsy). 2. Patients with a history of acute or chronic confusion. 3. Patients taking centrally acting drugs (e.g., antidepressants, antiparkinsonian drugs, sedatives, monoamine oxidase inhibitors), or alcohol abusers. 4. Patients who have medical disorders predisposing to delirium (e.g. cachexia, thyroid dysfunction, renal failure).

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Melatonin
The patients were assessed using the Memorial Delirium Assessment Scale (MDAS) after the operation at 30, 60, and 90 min. Melatonin was shown to reduce delirium from 41.6% to 16.6% at 60 minutes, and the significant reduction was at 90 minutes (0%) when compared to both groups. Thus, melatonin was found to be successful in decreasing postoperative delirium when administered preoperatively.
Other:
No intervention
No intervention was used.
Drug:
Midazolam
7.5 mg of Midazolam orally.

Locations

Country Name City State
Iraq Al-Kadhemya Private Hospital Baghdad
Iraq Ghazi Al-Hariri Teaching Hospital Baghdad

Sponsors (1)

Lead Sponsor Collaborator
University of Baghdad

Country where clinical trial is conducted

Iraq, 

Outcome

Type Measure Description Time frame Safety issue
Primary The efficacy of oral Melatonin in preventing Postoperative Delirium after general anesthesia This interventional trial is done to determine the efficacy of preoperative melatonin administration in reducing postoperative delirium rates. 1 week
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