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Magnesium Sulphate Versus Fentanyl Sedation During Burr-hole Surgery

Primary Purpose

Monitored Anesthesia Care

Status
Completed
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Magnesium Sulphate
Fentanyl
Propofol
Sponsored by
Kasr El Aini Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Monitored Anesthesia Care focused on measuring magnesium sulphate, fentanyl, propofol, monitored anesthesia care, burr-hole evacuation, chronic subdural hematoma

Eligibility Criteria

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

Inclusion Criteria:

  • patients with unilateral, chronic subdural hematoma,
  • aged above 50 years,
  • american society of anesthesiologist-physical status (ASA-PS) grade I-II,
  • Glasgow coma scale of 14-15.

Exclusion Criteria:

  • Patients with hypertension (Systolic blood pressure > 160 mmHg),
  • bradycardia (<50 bpm),
  • ischemic heart disease,
  • second- or third-degree heart block,
  • long-term abuse of or addiction to opioids, and sedative-hypnotic drugs (>6 months),
  • allergy to study drugs
  • neuropsychiatric diseases
  • patients with predicted difficult airway
  • patients with history of obstructive sleep apnea
  • patients with deviation in the surgical technique
  • inadequacy of local anesthesia

Sites / Locations

  • Kasr Alaini Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Group M

Group F

Arm Description

magnesium sulphate as adjuvant to propofol

fentanyl as adjuvant to propofol

Outcomes

Primary Outcome Measures

average systolic blood pressure
mmgh

Secondary Outcome Measures

ephedrine use
mg
Total amount of Propofol consumption
mg
Total number of intraoperative patient's movements
defined as those likely to interfere with surgical procedure such as bending of hand and/or leg and movement of head
Systolic blood pressure
mmgh
Diastolic blood pressure
mmgh
Heart rate
bpm
Surgeon satisfaction score
1, extremely dissatisfied; 2, not satisfied but able to manage; 3, satisfied; 4, extremely satisfied.
Ramsay sedation scale
Ramsey 1 Anxious, agitated, restless Ramsey 2 Cooperative, oriented, tranquil Ramsey 3 Responsive to commands only If Asleep Ramsey 4 Brisk response to light glabellar tap or loud auditory stimulus Ramsey 5 Sluggish response to light glabellar tap or loud auditory stimulus Ramsey 6 No response to light glabellar tap or loud auditory stimulus
Visual Analogue Scale (VAS) for pain
10 cm horizontal line on which the patient's pain intensity is represented by a point between the extremes of 0=no pain at all and 10 cm = worst pain imaginable."
atropine use
mg
first rescue analgesic during 1 hour post operative
incidence of patients requiring analgesics
postoperative nausea and vomiting
incidence

Full Information

First Posted
February 24, 2019
Last Updated
April 11, 2021
Sponsor
Kasr El Aini Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03854812
Brief Title
Magnesium Sulphate Versus Fentanyl Sedation During Burr-hole Surgery
Official Title
Magnesium Sulphate Versus Fentanyl as Adjuvants to Propofol for Monitored Anesthesia Care During Burr-hole Surgery for Chronic Subdural Hematoma: Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
March 1, 2019 (Actual)
Primary Completion Date
October 12, 2019 (Actual)
Study Completion Date
October 12, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kasr El Aini Hospital

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
MgSO4 was found to reduce the perioperative anesthetic and analgesic requirements when used as an adjuvant to general anesthesia. Fentanyl is a potent opioid and used as adjuvant to other sedatives in awake craniotomy procedure. No study, to the best of our knowledge had evaluated fentanyl continuous infusion, nor MgSo4 infusion as adjuvant sedative agents to propofol during Burr-hole surgery. The aim of this study is to evaluate and compare MgSO4 versus fentanyl continuous infusions for conscious sedation in patients undergoing burr hole surgery for evacuation of subdural hematoma with local infiltration.
Detailed Description
All participants or their proxy will be informed about the anesthetic techniques and the operative procedure and will provide written informed consent before enrollment in the study. The eligible patients will be randomly divided by computer designed lists and then will be concealed in closed envelopes into the two study groups. A research assistant who will not be involved in patient management will be responsible for opening the envelope, group assignment and drugs preparation. Anesthetic management Pre-induction No premedication will be administered. Upon arrival to the operating theater, an intravenous (IV) cannula will be placed, and standard monitors, including 5-lead electrocardiogram, noninvasive arterial blood pressure monitor, and pulse oximetry, will be applied. Oxygen supplementation at fraction of inspired oxygen (FiO2) of 0.35 will be achieved through a suitable air entrainment mask. Bispectral index (BIS: apparatus info) will be applied before starting the drug infusions and will be used for maintenance of sedation during operation. Induction of anesthesia Group M (n=17): will receive a loading of 50 mg/kg in 15 minutes of Magnesium sulphate, and will be followed by continuous infusion at 1 ml/kg/h of 15 mg/ml solution Group F (n=17): will receive a loading of 1 mcg/kg in over 15 minutes of fentanyl then will receive continuous infusion starting at 1 ml /kg/h. of 0.5 mcg/ml solution Both groups will be given 0.5-1.5 mg/kg bolus of propofol over 10 minutes to achieve target Ramsay sedation scale (RSS) of 3 (respond to command), if RSS afterwards does not reach 3 a supplementary bolus dose of 0.2 mg/kg propofol will be given to the patients, and will be followed by 1-2.5 mg/kg/hr infusion to maintain Intraoperative BIS readings between 60 - 80. Intraoperative management After achieving the target sedation level (RSS of 3), surgeons will infiltrate the surgical site with 20 mL of a local anesthetic solution containing 10 mL of 0.5% bupivacaine and 10 mL of 2% lidocaine with adrenaline at least 5 minutes before surgical incision. After performing burr-hole craniotomy soaked pledgets with lidocaine will be applied to anaesthetize the dura, the dura will be then opened, and the hematoma will be evacuated. The Infusion of sedatives will be ceased after skin closure. Intraoperative patient's movements (defined as those which may interfere with the surgical conduct such as twisting of hand and/or leg and head mobility) will be managed by reassurance and support for 30 seconds. However, when movements continue, a bolus dose of propofol of 0.5 mg/kg will be given then infusion dose will be increased till the maximum dose (2.5mg/kg/hr) to regain BIS sedation score between 60-80. If the patient starts to move again the same sequence will be repeated. Minute movements of other body parts as well as movements of fingers or toes that unlikely to hinder the operative intervention, will be deemed insignificant to be documented. Induction of general anesthesia will be only indicated if satisfactory surgical conditions will not be attained by the rescue propofol. Intraoperative bradycardia and tachycardia (defined as heart rate (HR) < 45 bpm or > 120 bpm respectively) will be treated with intravenous atropine 0.2 mg, or propranolol 0.5-1 mg respectively. Hypertension and hypotension (defined as a more than 25% increase or decrease from baseline respectively) will be treated with nitroglycerine (0.1-10 mcg/min) or ephedrine (5 mg) respectively. Postoperative management All patients will be transferred to the post-anesthesia care unit (PACU) after surgery where they will be closely monitored with the aid of five-lead electrocardiography and non-invasive arterial blood pressure, peripheral oxygen saturation (SpO2), and respiratory rate readings using an automated system for 24 h after surgery. Postoperative pain intensity will be assessed using VAS score at 1, 2, 3 and 6 hours after PACU admission. If VAS score exceeds 3, 30 mg of ketorolac will be administered.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Monitored Anesthesia Care
Keywords
magnesium sulphate, fentanyl, propofol, monitored anesthesia care, burr-hole evacuation, chronic subdural hematoma

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group M
Arm Type
Active Comparator
Arm Description
magnesium sulphate as adjuvant to propofol
Arm Title
Group F
Arm Type
Active Comparator
Arm Description
fentanyl as adjuvant to propofol
Intervention Type
Drug
Intervention Name(s)
Magnesium Sulphate
Other Intervention Name(s)
magnesium sulfate
Intervention Description
a loading of 50 mg/kg in 15 minutes of Magnesium sulphate, and will be followed by continuous infusion at 1 ml/kg/h of 15 mg/ml solution
Intervention Type
Drug
Intervention Name(s)
Fentanyl
Intervention Description
loading of 1 mcg/kg in over 15 minutes of fentanyl then will receive continuous infusion starting at 1 ml /kg/h. of 0.5 mcg/ml solution
Intervention Type
Drug
Intervention Name(s)
Propofol
Intervention Description
0.5-1.5 mg/kg bolus of propofol over 10 minutes to achieve target Ramsay sedation scale (RSS) of 3 (respond to command), if RSS afterwards does not reach 3 a supplementary bolus dose of 0.2 mg/kg propofol will be given to the patients, and will be followed by 1-2.5 mg/kg/hr infusion to maintain Intraoperative BIS readings between 60 - 80
Primary Outcome Measure Information:
Title
average systolic blood pressure
Description
mmgh
Time Frame
after induction of conscious sedation till end of procedure
Secondary Outcome Measure Information:
Title
ephedrine use
Description
mg
Time Frame
after induction of conscious sedation till end of procedure
Title
Total amount of Propofol consumption
Description
mg
Time Frame
after induction of conscious sedation till end of procedure
Title
Total number of intraoperative patient's movements
Description
defined as those likely to interfere with surgical procedure such as bending of hand and/or leg and movement of head
Time Frame
after induction of conscious sedation till end of procedure
Title
Systolic blood pressure
Description
mmgh
Time Frame
upon arrival at the operating room, after induction of conscious sedation, at skin incision, at 1,2,5,10,15 min and 10 min after skin incision, every 15 minutes intraoperative, on arrival at PACU, 5,10,15,30 min and 1 hour at the PACU
Title
Diastolic blood pressure
Description
mmgh
Time Frame
upon arrival at the operating room, after induction of conscious sedation, at skin incision, at 1,2,5,10,15 min and 10 min after skin incision, every 15 minutes intraoperative, on arrival at PACU, 5,10,15,30 min and 1 hour at the PACU
Title
Heart rate
Description
bpm
Time Frame
upon arrival at the operating room, after induction of conscious sedation, at skin incision, at 1,2,5,10,15 min and 10 min after skin incision, every 15 minutes intraoperative, on arrival at PACU, 5,10,15,30 min and 1 hour at the PACU
Title
Surgeon satisfaction score
Description
1, extremely dissatisfied; 2, not satisfied but able to manage; 3, satisfied; 4, extremely satisfied.
Time Frame
30 minutes after the end of the surgery
Title
Ramsay sedation scale
Description
Ramsey 1 Anxious, agitated, restless Ramsey 2 Cooperative, oriented, tranquil Ramsey 3 Responsive to commands only If Asleep Ramsey 4 Brisk response to light glabellar tap or loud auditory stimulus Ramsey 5 Sluggish response to light glabellar tap or loud auditory stimulus Ramsey 6 No response to light glabellar tap or loud auditory stimulus
Time Frame
15 and 30 minutes postoperative
Title
Visual Analogue Scale (VAS) for pain
Description
10 cm horizontal line on which the patient's pain intensity is represented by a point between the extremes of 0=no pain at all and 10 cm = worst pain imaginable."
Time Frame
at 15 minutes, 30 minutes, 1hr, 2 hrs. 3hrs and 6 hrs after PACU admission
Title
atropine use
Description
mg
Time Frame
after induction of conscious sedation till end of procedure
Title
first rescue analgesic during 1 hour post operative
Description
incidence of patients requiring analgesics
Time Frame
1 hour postoperative
Title
postoperative nausea and vomiting
Description
incidence
Time Frame
first 24 hours in the postoperative period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with unilateral, chronic subdural hematoma, aged above 50 years, american society of anesthesiologist-physical status (ASA-PS) grade I-II, Glasgow coma scale of 14-15. Exclusion Criteria: Patients with hypertension (Systolic blood pressure > 160 mmHg), bradycardia (<50 bpm), ischemic heart disease, second- or third-degree heart block, long-term abuse of or addiction to opioids, and sedative-hypnotic drugs (>6 months), allergy to study drugs neuropsychiatric diseases patients with predicted difficult airway patients with history of obstructive sleep apnea patients with deviation in the surgical technique inadequacy of local anesthesia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maha mostafa, MD
Organizational Affiliation
kasr el aini
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kasr Alaini Hospital
City
Cairo
ZIP/Postal Code
11562
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
28494889
Citation
Rodriguez-Rubio L, Nava E, Del Pozo JSG, Jordan J. Influence of the perioperative administration of magnesium sulfate on the total dose of anesthetics during general anesthesia. A systematic review and meta-analysis. J Clin Anesth. 2017 Jun;39:129-138. doi: 10.1016/j.jclinane.2017.03.038. Epub 2017 Apr 7.
Results Reference
background
PubMed Identifier
18040111
Citation
Sinha PK, Koshy T, Gayatri P, Smitha V, Abraham M, Rathod RC. Anesthesia for awake craniotomy: a retrospective study. Neurol India. 2007 Oct-Dec;55(4):376-81. doi: 10.4103/0028-3886.33308.
Results Reference
background
PubMed Identifier
8513521
Citation
Gignac E, Manninen PH, Gelb AW. Comparison of fentanyl, sufentanil and alfentanil during awake craniotomy for epilepsy. Can J Anaesth. 1993 May;40(5 Pt 1):421-4. doi: 10.1007/BF03009510.
Results Reference
background

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Magnesium Sulphate Versus Fentanyl Sedation During Burr-hole Surgery

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