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Pregabalin Versus Dexmedetomidine for Delirium Prevention After Cardiac Surgery

Primary Purpose

Pregabalin, Dexmedetomidine, Delirium

Status
Recruiting
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Pregabalin
Dexmedetomidine
Sponsored by
Tanta University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pregabalin

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: ≥ 65 years of age both genders American Society of Anesthesiologists (ASA) physical status classification II or III scheduled for cardiac surgery. Exclusion Criteria: Patients who had history of psychiatric diseases; inability to communicate; previous history of POD; preoperative sick sinus syndrome. Allergy/sensitivity to pregabalin or dexmedetomidine. Severe bradycardia (heart rate <50 beat per minute). Second-degree or above atrioventricular block without pacemaker. Severe hepatic or renal insufficiency. Previous cardiac or thoracic surgery. Known diagnosis of depression or other major psychiatric diseases. Cognitive impairment or inability to cooperate with the study. Renal insufficiency, and history of substance abuse.

Sites / Locations

  • Tanta UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

pregabalin group

dexmedetomidine group

Arm Description

patients will receive pregabalin capsules (75 mg) will be given 2 h prior to induction of anesthesia and every 12 h for 24h postoperatively by nasogastric tube or orally. Patients will receive IV saline as placebo with the same rate of dexmedetomidine.

patients in the dexmedetomidine group will receive after induction of GA a bolus dose of 0.4 μg/kg dexmedetomidine (over a period of 10 to 20 min) followed by an infusion of 0.2 to 0.7 μg/kg/h. Patients will receive placebo 2 h prior to induction of anesthesia and every 12 h for 24h postoperatively by nasogastric tube or orally. If patients are hemodynamically unstable, the bolus dose will be omitted. The infusion of dexmedetomidine will be continued for a maximum period of 24 h. Dexmedetomidine infusion will be not discontinued before extubation.

Outcomes

Primary Outcome Measures

Incidence of Delirium
Assessment of delirium will be performed preoperatively and postoperatively at 12-h intervals or as needed according to the patient's condition using the confusion assessment method (CAM)

Secondary Outcome Measures

Pain score
Postoperative pain (using VAS) at rest and movement will be measured at PACU, 1h, 2hr. 4hr, 6hr, 8hr, 12hr, 18hr, and 24hrs postoperative. The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be').
Postoperative opioid consumption
Patients will receive single 3 mg dose of intravenous morphine and patient control analgesia (PCA) will be started with a programmable PCA pump using the following settings: basal morphine infusion 1 mg/h, bolus dose 1 mg, and lockout time 20 minutes.
Sedation
Sedation level will be recorded using Sedation Agitation Scale
Length of hospital stay
Patients will stay in hospital for one month

Full Information

First Posted
November 26, 2022
Last Updated
March 7, 2023
Sponsor
Tanta University
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1. Study Identification

Unique Protocol Identification Number
NCT05640479
Brief Title
Pregabalin Versus Dexmedetomidine for Delirium Prevention After Cardiac Surgery
Official Title
Pregabalin Versus Dexmedetomidine for Delirium Prevention After Cardiac Surgery: A Randomized Double-Blind Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 15, 2022 (Actual)
Primary Completion Date
May 15, 2023 (Anticipated)
Study Completion Date
May 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tanta University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to compare the effect of perioperative administration of pregabalin versus dexmedetomidine on the prevalence and lasting duration of delirium in elderly patients after cardiac surgery.
Detailed Description
Pregabalin is a beta-isobutyl of GABA with chemical similarity to gabapentin . Pregabalin binds to the alpha-2-delta subgroup of calcium channels, thereby reducing excitatory neurotransmitter release and preventing hyperalgesia and central sensitization . Pregabalin is used as anticonvulsant but has also been used as analgesic for neuropathic pain and, lately, for postoperative pain, in an attempt to reduce opioid consumption and prevent progression to chronic pain. Dexmedetomidine with its broad range of effects including easily controllable sedation, analgesia, and anxiolysis still enables the caring medical team to interact with the patient. It reduces the activity while still maintaining the reactivity of neurons in the locus coeruleus. Therefore, it is an appealing alternative to traditional sedatives such as propofol and benzodiazepines.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregabalin, Dexmedetomidine, Delirium

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
The research solutions will be formulated by a devoted pharmacist who had no further involvement in the trial. Intraoperative and postoperative parameters will be examined by a second anesthesiologist who was unaware of group assignment.
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
pregabalin group
Arm Type
Active Comparator
Arm Description
patients will receive pregabalin capsules (75 mg) will be given 2 h prior to induction of anesthesia and every 12 h for 24h postoperatively by nasogastric tube or orally. Patients will receive IV saline as placebo with the same rate of dexmedetomidine.
Arm Title
dexmedetomidine group
Arm Type
Active Comparator
Arm Description
patients in the dexmedetomidine group will receive after induction of GA a bolus dose of 0.4 μg/kg dexmedetomidine (over a period of 10 to 20 min) followed by an infusion of 0.2 to 0.7 μg/kg/h. Patients will receive placebo 2 h prior to induction of anesthesia and every 12 h for 24h postoperatively by nasogastric tube or orally. If patients are hemodynamically unstable, the bolus dose will be omitted. The infusion of dexmedetomidine will be continued for a maximum period of 24 h. Dexmedetomidine infusion will be not discontinued before extubation.
Intervention Type
Drug
Intervention Name(s)
Pregabalin
Intervention Description
patients will receive pregabalin capsules (75 mg) will be given 2 h prior to induction of anesthesia and every 12 hours
Intervention Type
Drug
Intervention Name(s)
Dexmedetomidine
Intervention Description
patients will receive dexmedetomidine after induction of GA a bolus dose of 0.4 μg/kg dexmedetomidine (over a period of 10 to 20 min) followed by an infusion of 0.2 to 0.7 μg/kg/h
Primary Outcome Measure Information:
Title
Incidence of Delirium
Description
Assessment of delirium will be performed preoperatively and postoperatively at 12-h intervals or as needed according to the patient's condition using the confusion assessment method (CAM)
Time Frame
24hour postoperatively
Secondary Outcome Measure Information:
Title
Pain score
Description
Postoperative pain (using VAS) at rest and movement will be measured at PACU, 1h, 2hr. 4hr, 6hr, 8hr, 12hr, 18hr, and 24hrs postoperative. The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be').
Time Frame
24 hours postoperatively
Title
Postoperative opioid consumption
Description
Patients will receive single 3 mg dose of intravenous morphine and patient control analgesia (PCA) will be started with a programmable PCA pump using the following settings: basal morphine infusion 1 mg/h, bolus dose 1 mg, and lockout time 20 minutes.
Time Frame
24 hours postoperatively
Title
Sedation
Description
Sedation level will be recorded using Sedation Agitation Scale
Time Frame
24 hours postoperatively
Title
Length of hospital stay
Description
Patients will stay in hospital for one month
Time Frame
One month postoperatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥ 65 years of age both genders American Society of Anesthesiologists (ASA) physical status classification II or III scheduled for cardiac surgery. Exclusion Criteria: Patients who had history of psychiatric diseases; inability to communicate; previous history of POD; preoperative sick sinus syndrome. Allergy/sensitivity to pregabalin or dexmedetomidine. Severe bradycardia (heart rate <50 beat per minute). Second-degree or above atrioventricular block without pacemaker. Severe hepatic or renal insufficiency. Previous cardiac or thoracic surgery. Known diagnosis of depression or other major psychiatric diseases. Cognitive impairment or inability to cooperate with the study. Renal insufficiency, and history of substance abuse.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Islam Morsy, MD
Phone
00201093387374
Email
eslam.morsy@med.tanta.edu.eg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohammed S El Sharkawy, MD
Organizational Affiliation
Assistant Lecturer of Anesthesiology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hussein G Almawardy, MD
Organizational Affiliation
Lecturer of Anesthesiology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tanta University
City
Tanta
State/Province
ElGharbiaa
ZIP/Postal Code
31527
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mohammed S ElSharkawy, MD
Phone
00201148207870
Email
mselsharkawy@med.tanta.edu.eg
First Name & Middle Initial & Last Name & Degree
Islam Morsy, MD
First Name & Middle Initial & Last Name & Degree
Mohammed S El Sharkawy, MD
First Name & Middle Initial & Last Name & Degree
Hussein G Almawardy, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The data will be upon reasonable request from the principal investigator
IPD Sharing Time Frame
for one year after completion of the study

Learn more about this trial

Pregabalin Versus Dexmedetomidine for Delirium Prevention After Cardiac Surgery

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