Pregnancy Clinical Trial
Official title:
A Randomized Controlled Trial of Epidural Volume Extension During a Combined Spinal-Epidural Technique for Labor Analgesia.
Combined spinal-epidurals (CSE) involve the injection of pain relief medication into the cerebral spinal fluid (CSF) and the insertion of an epidural catheter in the epidural space to continue to give pain relief medication. During a CSE, after injection of the medication in the CSF and before inserting the epidural catheter, if normal saline is injected into the epidural space, there may be an increase in pain relief and an increase in the level of numbness. This injection of saline in the epidural space to increase pain relief and numbness is termed epidural volume extension (EVE). The purpose of this study is to determine if there is a benefit for EVE to improve labor analgesia (pain relief) using CSE in pregnant laboring patients.
Regional analgesia (pain relief) for labor can be an epidural, a spinal or a combination of
the two. Combined spinal-epidurals (CSE) are popular because of their rapid pain relief and
high patient satisfaction. At the IWK Health Centre, many anesthesiologists routinely use
this method of pain relief. It involves the injection of pain relief medication into the
cerebral spinal fluid (CSF) and the insertion of an epidural catheter (slim plastic tube) in
the epidural space to continue to give pain relief medication. The epidural space is located
just outside the CSF. In order to insert the epidural catheter, some anesthesiologists
inject 2-4 ml of saline in the epidural space to help the catheter go in. During a CSE,
after injection of the medication in the CSF and before inserting the epidural catheter, if
normal saline is injected into the epidural space, there may be an increase in pain relief
and an increase in the level of numbness. This injection of saline in the epidural space to
increase pain relief and numbness is termed epidural volume extension (EVE).
Thus far, studies on EVE have all been done in patients undergoing surgery with spinal
anesthesia and not solely for analgesia. The purpose of this study is to determine if there
is a benefit for EVE to improve labor analgesia (pain relief) using CSE. We will study 60
women requesting labor pain relief. Half these women will receive a CSE without EVE, which
is the present standard of care. The other half will receive a CSE with 10 ml of saline for
EVE before inserting the epidural catheter. We will then determine if there is a benefit for
EVE by observing for a difference between the two groups with respect to the level of
numbness, the amount and speed of pain relief and the intensity of leg weakness. We
hypothesize that injecting 10 ml of saline for EVE using CSE may improve the amount and
speed of pain relief while decreasing side effects such as leg weakness. If there were a
benefit to EVE, this would be a simple and inexpensive method for improving pain relief in
laboring women.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor), Primary Purpose: Treatment
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