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CSE for Labour Analgesia: A Comparison of Two Intrathecal Regimens (SSS)

Primary Purpose

Labor Pain

Status
Completed
Phase
Phase 4
Locations
Nigeria
Study Type
Interventional
Intervention
Bupivacaine-fentanyl
Bupivacaine-fentanyl morphine
Sponsored by
Sarah Beckley
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Labor Pain focused on measuring Single Shot Spinal, Intrathecal narcotics, Morphine, Fentanyl, Labour Analgesia

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Parturients in active labour >4cm dilatation
  • American Society of Anesthesiologists (ASA) classification I and II

Exclusion Criteria:

  • Significant co-morbidities like uncontrolled hypertension or diabetes
  • Maternal hemorrhage with hypotension
  • Significant bleeding/clotting disorders

Sites / Locations

  • Lagos Island Maternity Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

BF

BFM

Arm Description

Interventions: Intrathecal administration -Bupivacaine 2.5mg (0.5ml) + Fentanyl 25mcg (0.5ml) + 1ml sterile water in one shot Ephedrine 3-5mg in aliquots in the event of hypotension Promethazine 12.5 - 25mg in the event of vomiting or significant pruritus naloxone 2mcg/kg in the event of respiratory distress

Interventions: Intrathecal administration - Bupivacaine 2.5mg (0.5ml) + fentanyl 25mcg (0.5ml) + 0.25mg morphine (0.25ml) + 0.75ml sterile water in one shot ephedrine 3-5mg in aliquots for hypotension Promethazine 12.5 - 25mg for vomiting or significant pruritus Naloxone 2mcg/kg in the event of respiratory distress

Outcomes

Primary Outcome Measures

Time to First painless contraction (TFC)
This is the onset of action of the drugs. The time duration from the initiation of the block at time zero to the point where there is significant drop in the Numerical Rating Scale (NRS) to 2 or less
Time to First Request for Analgesia (TFA)
This is the duration of action of the block. Time from initiation of the block to time the pain score is up to 6 or more. It is expected that after onset of the block (TFC) the pain would first become negligible or absent and after a period of time, it would gradually increase as the drug wears off. If the pain becomes moderate at a NRS of 6 or the patient requests for analgesia, the time would be noted and the epidural would be activated.

Secondary Outcome Measures

Delivery before TFA or delivery after TFA
Qualitative variable. determines if rescue analgesia was needed (if the epidural needed to be activated) or if the spinal was adequate for the duration of labour
Maternal Satisfaction
Parturients perception of if analgesia was Adequate, Inadequate or Not Sure
Side effects
Presence of side effects like respiratory depression, pruritus, or vomiting

Full Information

First Posted
April 9, 2017
Last Updated
July 15, 2018
Sponsor
Sarah Beckley
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1. Study Identification

Unique Protocol Identification Number
NCT03117595
Brief Title
CSE for Labour Analgesia: A Comparison of Two Intrathecal Regimens
Acronym
SSS
Official Title
Combined Spinal Epidural Analgesia in Labour: A Comparison of Two Intrathecal Regimens of Single Shot Spinal
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
November 23, 2017 (Actual)
Primary Completion Date
February 27, 2018 (Actual)
Study Completion Date
April 25, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Sarah Beckley

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Analgesia in labour is not readily available in many parts of Sub-Saharan Africa. The overall cost of Epidural services in terms of human personnel and financial implication makes this inaccessible to many women in labour. Thus, a cheaper, less technically demanding and easier option that can produce as much satisfaction for the parturient and would allow her participate in the second stage of labour by being able to bare down is being studied. The Single Shot Spinal (SSS) would provide pain relief in these women however its draw back is its time limitation as the option of a top up is not available. Two regimen of drug options would be considered using opioids. These would be compared to see how well they are able to provide analgesia in women who hitherto have had vaginal birth. Their onset, duration of action and possible side effects would be compared. NULL HYPOTHESIS: Single Shot Spinal with Bupivacaine Fentanyl (BF) cannot provide a statistically significant difference in labour analgesia in comparison with Bupivacaine Fentanyl Morphine (BFM) ALTERNATE HYPOTHESIS: Single Shot Spinal with BF can provide a statistically significant difference in labour in comparison with BFM
Detailed Description
A double blinded randomized study comparing 2 intrathecal mixtures for labour analgesia. 94 multiparous parturients in active labour who have given informed consent would be recruited into the study. They would be randomly allocated into 2 groups using simple random sampling. An Assistant would know the code and prepare the intrathecal solutions. Baseline vitals would be taken and patient's pain score noted. Due protocol would be followed and a combined spinal epidural sited but with the epidural not activated until the effect of the spinal wears off. Routine monitoring would be done and various parameters and indices noted. Where the effect of the spinal lasts the duration of labour thus no need to activate the epidural, this would also be noted. Data would be analysed using Statistical Package of Social Sciences (SPSS) version 20.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Labor Pain
Keywords
Single Shot Spinal, Intrathecal narcotics, Morphine, Fentanyl, Labour Analgesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
2 groups that would remain with the randomly picked intervention throughout the study duration
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
a double blinded study. The participant and the Physician giving the treatment who would also evaluate the participant during the duration of the study are masked. However, the Assistant who is in charge of the randomization process and has the code and so would prepare the drugs is not blinded. The non-blinded Assistant would be available to break the code in the event of any adverse reactions.
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BF
Arm Type
Active Comparator
Arm Description
Interventions: Intrathecal administration -Bupivacaine 2.5mg (0.5ml) + Fentanyl 25mcg (0.5ml) + 1ml sterile water in one shot Ephedrine 3-5mg in aliquots in the event of hypotension Promethazine 12.5 - 25mg in the event of vomiting or significant pruritus naloxone 2mcg/kg in the event of respiratory distress
Arm Title
BFM
Arm Type
Active Comparator
Arm Description
Interventions: Intrathecal administration - Bupivacaine 2.5mg (0.5ml) + fentanyl 25mcg (0.5ml) + 0.25mg morphine (0.25ml) + 0.75ml sterile water in one shot ephedrine 3-5mg in aliquots for hypotension Promethazine 12.5 - 25mg for vomiting or significant pruritus Naloxone 2mcg/kg in the event of respiratory distress
Intervention Type
Drug
Intervention Name(s)
Bupivacaine-fentanyl
Intervention Description
Dosages as previously written
Intervention Type
Drug
Intervention Name(s)
Bupivacaine-fentanyl morphine
Intervention Description
Dosage as previously written
Primary Outcome Measure Information:
Title
Time to First painless contraction (TFC)
Description
This is the onset of action of the drugs. The time duration from the initiation of the block at time zero to the point where there is significant drop in the Numerical Rating Scale (NRS) to 2 or less
Time Frame
time zero to first painless contraction estimated 15 minutes
Title
Time to First Request for Analgesia (TFA)
Description
This is the duration of action of the block. Time from initiation of the block to time the pain score is up to 6 or more. It is expected that after onset of the block (TFC) the pain would first become negligible or absent and after a period of time, it would gradually increase as the drug wears off. If the pain becomes moderate at a NRS of 6 or the patient requests for analgesia, the time would be noted and the epidural would be activated.
Time Frame
Time zero till NRS > 6 estimated 180 minutes
Secondary Outcome Measure Information:
Title
Delivery before TFA or delivery after TFA
Description
Qualitative variable. determines if rescue analgesia was needed (if the epidural needed to be activated) or if the spinal was adequate for the duration of labour
Time Frame
duration of labour estimated 180 minutes
Title
Maternal Satisfaction
Description
Parturients perception of if analgesia was Adequate, Inadequate or Not Sure
Time Frame
up to 300 minutes
Title
Side effects
Description
Presence of side effects like respiratory depression, pruritus, or vomiting
Time Frame
up to 180 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: Parturients in active labour >4cm dilatation American Society of Anesthesiologists (ASA) classification I and II Exclusion Criteria: Significant co-morbidities like uncontrolled hypertension or diabetes Maternal hemorrhage with hypotension Significant bleeding/clotting disorders
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Olaniyi Oladapo, MBBS,FMCA, FWACS
Organizational Affiliation
School of Anaesthetic Studies, Health Service Commission, Lagos State
Official's Role
Study Chair
Facility Information:
Facility Name
Lagos Island Maternity Centre
City
Lagos
Country
Nigeria

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
17872679
Citation
Minty RG, Kelly L, Minty A, Hammett DC. Single-dose intrathecal analgesia to control labour pain: is it a useful alternative to epidural analgesia? Can Fam Physician. 2007 Mar;53(3):437-42.
Results Reference
background
PubMed Identifier
10700784
Citation
Lee BB, Ngan Kee WD, Hung VY, Wong EL. Combined spinal-epidural analgesia in labour: comparison of two doses of intrathecal bupivacaine with fentanyl. Br J Anaesth. 1999 Dec;83(6):868-71. doi: 10.1093/bja/83.6.868.
Results Reference
background
PubMed Identifier
12818975
Citation
Hess PE, Vasudevan A, Snowman C, Pratt SD. Small dose bupivacaine-fentanyl spinal analgesia combined with morphine for labor. Anesth Analg. 2003 Jul;97(1):247-52, table of contents. doi: 10.1213/01.ane.0000066520.30763.b8.
Results Reference
background

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CSE for Labour Analgesia: A Comparison of Two Intrathecal Regimens

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