Cardiac Effects of Oxytocin Administrated During Cesarean Section, Signs of Myocardial Ischemia
Primary Purpose
Myocardial Ischemia, Hypotension, Bloodloss
Status
Completed
Phase
Phase 4
Locations
Sweden
Study Type
Interventional
Intervention
oxytocin
oxytocin
Sponsored by
About this trial
This is an interventional treatment trial for Myocardial Ischemia focused on measuring oxytocin, ST depression, cesarean section, blood loss
Eligibility Criteria
Inclusion Criteria:
- Healthy women >/= 18 years scheduled to planned cesarean section
Exclusion Criteria:
- BMI > 35
- Multiple birth
- Complications to pregnancy
- Non proficiency in the Swedish language
Sites / Locations
- University hospital Uppsala
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
1
2
Arm Description
oxytocin 5 units
oxytocin, 10 units
Outcomes
Primary Outcome Measures
ST segment depression on ECG
Secondary Outcome Measures
mean arterial blood pressure, heart rate, blood loss and symptoms as chest pain
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00777166
Brief Title
Cardiac Effects of Oxytocin Administrated During Cesarean Section, Signs of Myocardial Ischemia
Official Title
Phase 4 Study of Oxytocin Used During Cesarean Section
Study Type
Interventional
2. Study Status
Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
December 2005 (undefined)
Primary Completion Date
July 2008 (Actual)
Study Completion Date
July 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Uppsala University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Oxytocin has cardio vascular effects as hypotension, tachycardia and possibly coronary spasm. The uterotonic effect of the drug is used during cesarean section, to minimize blood loss.ECG changes suggestive of cardiac ischemia (ST depression) has been showed in previous studies of patients undergoing cesarean section i regional anaesthesia. The effect of oxytocin on this outcome has not been investigated to any extent.
In the current study, we tested the hypothesis that there was no difference in occurrence of ECG changes (ST segment depression) between two doses of oxytocin. Participants were randomized to receive either 5 or 10 units of oxytocin in a double blinded fashion.
Main outcome measure is occurrence of significant ST depression on ECG. Secondary outcome measures are mean arterial pressure, heart rate, blood loss, symptoms as chest pain, shortness of breath and feeling of heaviness on the chest.
Detailed Description
All healthy term participants scheduled to undergo elective caesarean section under spinal anaesthesia at the Department of Obstetrics and Gynecology, University Hospital, Uppsala Sweden and who were > 18 years old, were candidates for inclusion in the study. .
The study was approved by the regional ethics committee and informed written consent was obtained from each participant.
ECGs were recorded by continuous ambulatory ECG (Holter) monitoring (GE Medical systems SEER/MARS, UK) during the peroperative period utilizing leads V3, V5 and avF. As secondary outcomes, symptoms as chest pain, shortness of breath and feeling of heaviness on the chest and, Troponin I levels 12 hours postoperatively, were recorded. Also, as secondary outcomes, differences in blood pressure, heart rate, and blood loss were measured.
Before induction of anaesthesia, patients received 1000 mL of lactated Ringer's solution intravenously. Thereafter an additional 500-1000 mL of lactated Ringer's solution or 500 mL Hydroxyethyl starch was infused if considered needed by the anaesthesiologist.
Spinal anaesthesia was established in the sitting position at lumbal interspace L2/L3 or L3/L4. Non invasive blood pressure (systolic, diastolic and mean arterial pressure, MAP) and heart rate was monitored every 2 minutes, throughout surgery. Oxytocin was given as an intravenous bolus dose immediately after clamping of the umbilical cord. Blood loss during the operation was estimated and recorded. During surgery, any spontaneous complaints by the patients of symptoms as chest pain, shortness of breath and feeling of heaviness on the chest, was recorded as well as duration of symptoms. Episodes of chest pain were assessed with the visual analogue scale (VAS).
Troponin I, as a marker of ischemic myocardial damage, was sampled 12 hours postoperatively.
The incidence of ECG changes related to different doses of intravenous bolus doses of oxytocin (5 and 10 units) during caesarean section is unknown. In a pilot study preceding the present study, 5 units oxytocin were administrated and the incidence of ECG changes was 15%. With the assumption that ECG changes could occur in 50% of subjects receiving 10 units oxytocin and based on 0.8 power to detect a significant difference (P = 0.05, two-sided), 25 patients were required for each study group. An interim analysis performed after inclusion of 50 patients revealed that ECG-changes occured in 8 and 24 % respectively in the two groups of 5 and 10 units of oxytocin. An additional 50 patients were allocated and a second interim analysis planned.
A computer-generated randomisation list with block of four was drawn up by a statistician and given to the pharmacy department who performed the randomisation. The procedure ensured allocation concealment.
All participants, health care providers, investigators and other persons (cardiologist) were blinded to treatment assignment for the duration of the study.
The Statistical Package for Social Sciences (SPSS) for Windows, version 15.0, was used (SPSS, Inc., Chicago, IL, USA). To compare group distributions the chi-squared test or Fisher's exact test was applied and the Mann-Whitney U-test or t-test for continuous variables. A p-value < 0.05 was considered to indicate a significant difference
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Ischemia, Hypotension, Bloodloss
Keywords
oxytocin, ST depression, cesarean section, blood loss
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
103 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
oxytocin 5 units
Arm Title
2
Arm Type
Active Comparator
Arm Description
oxytocin, 10 units
Intervention Type
Drug
Intervention Name(s)
oxytocin
Other Intervention Name(s)
syntocinon, Pitcotin
Intervention Description
oxytocin 5 units diluted with normal saline to a total volume of 10 mL
Intervention Type
Drug
Intervention Name(s)
oxytocin
Other Intervention Name(s)
Syntocinon, Pitcotin
Intervention Description
oxytocin 10 units diluted with normal saline to at total volume of 10 mL.
Primary Outcome Measure Information:
Title
ST segment depression on ECG
Time Frame
30 minutes
Secondary Outcome Measure Information:
Title
mean arterial blood pressure, heart rate, blood loss and symptoms as chest pain
Time Frame
60 minutes
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy women >/= 18 years scheduled to planned cesarean section
Exclusion Criteria:
BMI > 35
Multiple birth
Complications to pregnancy
Non proficiency in the Swedish language
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ove Axelsson, Professor
Organizational Affiliation
Uppsala University, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
University hospital Uppsala
City
Uppsala
Country
Sweden
12. IPD Sharing Statement
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Cardiac Effects of Oxytocin Administrated During Cesarean Section, Signs of Myocardial Ischemia
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