Postoperative Cognitive Dysfunction in Elderly and it's Relation With Sleep Disorders and Melanin Concentrating Hormone

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorMinia University

About this trial

The aim of this study is to explore the relationship between preoperative sleep disorders, melanin-concentrating hormone (MCH), and delayed neurocognitive recovery early after surgery in older adult patients undergoing spinal anesthesia.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients of both genders ageing 65 years or above.

ASA grade I to III.

Undergo elective lower limb surgery under spinal anesthesia

Agree to collect one's own CSF and blood samples

Disqualifiers

Past history of depression,anxiety,delirium and schizophrenia .

Past history of drug dependence.

Past history of dementia,including Alzheimer disease(AD).

Preoperative Montreal Cognitive Assessment (MoCA) score <26.

Trial population

A total of (50) patients candidate for elective lower limb surgery aged from 65 years of both sexes will be enrolled in this study.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

50 Participants
are grouped into 2 trial groups
Group A: Group A
Group B: Group B

Trial outcomes

Primary outcomes

1

To investigate the impact of preoperative sleep problems as indicators of delayed neurocognitive recovery (DNR) in elderly adults following spinal anesthesia.

By comparison between the two groups

Time frame
Baseline, one week, three months

Secondary outcomes

1

to investigate the predictive power of CSF and plasma MCH levels for delayed neurocognitive recovery (DNR) in older adults after spinal anesthesia

Time frame
Baseline one day before operation

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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