Actively Recruiting

Phase 4
Age: 18Years - 65Years
All Genders
NCT05593627

Effect of Lithium Carbonate on Postoperative Sleep and Cognitive Function in Patients Undergoing Heart Valve Surgery With Cardiopulmonary Bypass

Led by China Medical University, China · Updated on 2023-07-18

62

Participants Needed

1

Research Sites

160 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

It has been proved that lithium carbonate can prolong slow wave sleep with few or no side-effects. The aim of the present study is to evaluate postoperative sleep quality of patients undergoing heart valve surgery with cardiopulmonary bypass taken 250mg lithium carbonate after surgery.

CONDITIONS

Official Title

Effect of Lithium Carbonate on Postoperative Sleep and Cognitive Function in Patients Undergoing Heart Valve Surgery With Cardiopulmonary Bypass

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ethnic Chinese
  • Age between 18 and 65 years old
  • Undergoing heart valve surgery with cardiopulmonary bypass
Not Eligible

You will not qualify if you...

  • Preoperative Pittsburgh Sleep Quality Index global score higher than 6
  • Cognitive difficulties
  • Partial or complete gastrectomy
  • Previous esophageal surgery
  • Previous radiotherapy or surgery treatment
  • Inability to conform to study requirements
  • Body mass index over 30 kg/m2
  • Deprivation of decision-making rights by legal authority
  • Participation in another study within the past month
  • Recent use (within 3 months) of antibiotics, probiotics, prebiotics, symbiotics, hormonal medication, laxatives, proton pump inhibitors, insulin sensitizers, or traditional Chinese medicine

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

the First Hospital of China Medical University

Shenyang, Liaoning, China, 110001

Actively Recruiting

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Research Team

W

Wenfei Tan

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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