ET50 With Fentanyl for Post Caesarean Section Spinal Hypotension (ET-50-Fent)
Primary Purpose
Hypotension, Pregnancy
Status
Unknown status
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Bupivacaine with 15 micrograms of fentanyl
Sponsored by
About this trial
This is an interventional prevention trial for Hypotension focused on measuring Post spinal hypotension, Cesarian Section, ET50, Bupivacaine, Fentanyl
Eligibility Criteria
Inclusion Criteria:
- Patients 18 years or older, presenting for scheduled cesarean delivery to the C7 birthing centre.
Exclusion Criteria:
- Unable to communicate in English or French
- Multiple gestations
- Patients with hypertension
- Patients with contraindications to any drug or techniques used in the study
- BMI > 35
Sites / Locations
- Royal Victoria HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
2 ml Bupivacaine
1.5 ml Bupivacaine
Arm Description
2 ml Bupivacaine with 15 micrograms of fentanyl
1.5 ml Bupivacaine with 15 micrograms of fentanyl
Outcomes
Primary Outcome Measures
Sitting time to avoid hypotension
Sitting time required to avoid a drop of 20% of patient's baseline blood pressure or symptoms of hypotension in 50% of patients
Secondary Outcome Measures
Pain occurence
Full Information
NCT ID
NCT01896960
First Posted
July 2, 2013
Last Updated
June 20, 2014
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
1. Study Identification
Unique Protocol Identification Number
NCT01896960
Brief Title
ET50 With Fentanyl for Post Caesarean Section Spinal Hypotension
Acronym
ET-50-Fent
Official Title
The Time Required to Remain Sitting After Spinal Anesthesia With Fentanyl for 50% of Patients to Not Experience Hypotension.
Study Type
Interventional
2. Study Status
Record Verification Date
June 2014
Overall Recruitment Status
Unknown status
Study Start Date
July 2013 (undefined)
Primary Completion Date
June 2015 (Anticipated)
Study Completion Date
June 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Hypotension is extremely common after induction of spinal anesthesia for cesarean delivery. Anesthetic blockade of the sympathetic outflow of the spinal cord causes vasodilation, and is one cause of this hypotension. The higher the spread of the blockade will result in a higher incidence of hypotension. Injected hyperbaric medication has about 15 minutes to spread within the intrathecal space before it will be taken up by the nerve roots. The time that a patient remains in one position after medication injection will affect the spread of the resultant anesthetic block. A patient who is left sitting for a longer period of time after injection of hyperbaric medication will have a lower level of block than someone who is placed supine immediately. In this study, the investigators wish to use up down sequential analysis to determine the time period a patient should remain seated after intrathecal injection of hyperbaric bupivacaine and fentanyl that will result in a 50% rate of hypotension.
Detailed Description
Up down sequential analysis is a method developed by Dixon to determine the point where 50% of people will have a positive response and 50% will have a negative response to an intervention. It is a very powerful technique that has been used to determine the median effective dose (referred to as ED50) of many medications. Using this method, patient number 1 is given a certain amount of the intervention being studied. If patient 1 has the desired response, patient 2 in the series is given less of the intervention, and if patient 1 does not have the desired response, patient 2 is given more of the intervention. This is repeated through a series of patients until the dose where there is a 50% response rate is determined. In this study, the investigators wish to use up down sequential analysis to determine the time period a patient should remain seated after intrathecal injection of hyperbaric medication that result in a 50% rate of hypotension, what we will call the ET50 (Estimated Time for 50% of patients to have hypotension). The investigators would like to explore this relationship with 2 clinically used doses of hyperbaric bupivicaine.
Patients scheduled for cesarean delivery arrive in the birthing centre 1-2 The patients will be given the same anesthetic care routinely used in the birthing centre, except that the investigators will control the time that the patient remains seated after injection of intrathecal hyperbaric bupivacaine. The baseline blood pressure and heart rate will be recorded. After intravenous access is obtained, an infusion of normal saline will be commenced at a rate of 100 cc per hour. The patient will be brought to the operating room, and the standard monitors will be placed. The intravenous fluid will be administered at a rate of 500 ml per hour for one hour. The patient will be placed in a sitting position. The landmarks of the spinal canal will be identified with an ultrasound, then using sterile technique, an epidural catheter will be placed in the L2-L3 spinal interspace, and then a 27 gauge whitacre needle will be used to access the intrathecal space at the L4-L5 spinal interspace. After identification of the intrathecal space, hyperbaric bupivacaine will be injected over 30 seconds. The patient will then be left in the sitting position for the predetermined time. The patient will then be placed supine, with a 15 degree wedge under the right hip. The noninvasive blood pressure will be set to measure the blood pressure every minute. Hypotension will be defined as a drop in blood pressure to more than 20% of the patient's preoperative blood pressure. The medications used for treatment of hypotension will be left to the discretion of the treating anesthesiologist. The height of the anesthetic blockade will be measured bilaterally with ice at 1, 5, 10, 15, and 20 minutes after the patient has been placed supine. If the block has not reached T6 by 20 minutes after the patient has assumed the supine position, or if the patient experiences any pain during the cesarean delivery, 5 ml of 2% lidocaine will be administered through the epidural catheter. If this does not suitably manage the pain, the treating anesthesiologist will be allowed to manage the pain as they see fit.
Determination of the time in the sitting position :
The study patient will be considered a success if the duration of time in the sitting position results in no pre-delivery hypotension. The study patient will be considered a failure if the time spent in the sitting position results in pre-delivery hypotension. A patient will be considered an indeterminate result if the ice test fails to show a block reaching T6 by 15 minutes. A patient following a success will be left in the sitting position for 15 seconds less than the preceding patient, and the patient following a failure will be left in the sitting position for 15 seconds more than the preceding patient. A patient following an indeterminate result will remain in the sitting position for the same time as the preceding patient. The first patient in the series will be left in the sitting position for two minutes and half for the 1.5 ml bupivacaine and 6 minutes and half for the 2 ml bupivacaine after the injection of the intrathecal medication.
Dosage determination and blinding:
To see if ET50 is dependent on the dosage of medication given, we will determine the ET50 for 2 doses of hyperbaric bupivicaine with 15 micrograms of fentanyl. Both of the doses we will study are used routinely in clinical practice. Using a computerized randomization schedule, we will randomly assign patients to receive either 2 ml or 1.5 ml of 0.75% hyperbaric bupivacaine, for a total of 15 mg or 12.5 mg of bupivacaine respectively.
Recorded data:
The investigators will record the demographic data of the patient, including height, weight, age, gravidity, parity, weeks gestation, and reason for the cesarean delivery. The investigators will record the medical history of the patient, and medications that the patient takes. The investigators will record the admission heart rate, blood pressure and saturation. The investigators will record the time that the intrathecal medication is injected, and the time that that the patient remains seated after the spinal anesthesia has been commenced. The investigators will record the level of anesthetic blockade at 1,5,10,15,and 20 minutes after the patient has been placed supine. The investigators will record the blood pressure, and heart rate every minute after the patient has been placed supine until the baby has been delivered. The investigators will record any medications used to treat blood pressure before the baby has been born, and any medications used to treat breakthrough pain. The investigators will record the birth time, the baby gender, weight, apgar, and umbilical cord pH.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypotension, Pregnancy
Keywords
Post spinal hypotension, Cesarian Section, ET50, Bupivacaine, Fentanyl
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
2 ml Bupivacaine
Arm Type
Active Comparator
Arm Description
2 ml Bupivacaine with 15 micrograms of fentanyl
Arm Title
1.5 ml Bupivacaine
Arm Type
Active Comparator
Arm Description
1.5 ml Bupivacaine with 15 micrograms of fentanyl
Intervention Type
Drug
Intervention Name(s)
Bupivacaine with 15 micrograms of fentanyl
Intervention Description
Testing 2 doses of Bupivacaine (12.5 mg and 15 mg) with 15 micrograms fentanyl
Primary Outcome Measure Information:
Title
Sitting time to avoid hypotension
Description
Sitting time required to avoid a drop of 20% of patient's baseline blood pressure or symptoms of hypotension in 50% of patients
Time Frame
one hour
Secondary Outcome Measure Information:
Title
Pain occurence
Time Frame
One hour
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients 18 years or older, presenting for scheduled cesarean delivery to the C7 birthing centre.
Exclusion Criteria:
Unable to communicate in English or French
Multiple gestations
Patients with hypertension
Patients with contraindications to any drug or techniques used in the study
BMI > 35
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aly Elbahrawy, MD
Email
aly.elbahrawy@mail.mcgill.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Albert Moore, MD
Organizational Affiliation
McGill
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Victoria Hospital
City
Montreal
State/Province
Quebec
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Albert Moore, MD
Email
moore_albert@hotmail.com
12. IPD Sharing Statement
Citations:
PubMed Identifier
28741272
Citation
Moore A, El-Mouallem E, El-Bahrawy A, Kaufman I, Moustafa M, Derzi S, Hatzakorzian R, Lipishan W. An up-down determination of the required seated duration after intrathecal injection of bupivacaine and fentanyl for the prevention of hypotension during Cesarean delivery. Can J Anaesth. 2017 Oct;64(10):1002-1008. doi: 10.1007/s12630-017-0931-z. Epub 2017 Jul 24.
Results Reference
derived
Learn more about this trial
ET50 With Fentanyl for Post Caesarean Section Spinal Hypotension
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