The Effectiveness of Gabapentin for Post-operative Pain Following Cesarean Section
Primary Purpose
Pain
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
lactose
Gabapentin 300mg
Gabapentin 600mg
Sponsored by
About this trial
This is an interventional treatment trial for Pain focused on measuring Cesarean section, Gabapentin
Eligibility Criteria
Inclusion Criteria:
- 18 years or older
- full term singleton pregnancy
- undergoing elective cesarean delivery
Exclusion Criteria:
- Patients unable to communicate fluently in English
- Patients with American Society of Anesthesiologists (ASA) classification of 3 or greater
- Patients with history of epilepsy or chronic pain, or of use of anti-epileptic drugs or neuropathic analgesic drugs
- Patients with a history of opioid or intravenous drug abuse
- Patients with a known allergy or contra-indication to gabapentin, or to any other drugs used in this trial
- Patients who have refused spinal anaesthesia, or those in whom it is contra-indicated
- Patients with known congenital fetal abnormalities
- Patients who have taken antacid medication in the previous 24 hours
Sites / Locations
- Mount Sinai Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Placebo Comparator
Active Comparator
Active Comparator
Arm Label
Placebo
Gabapentin 300mg
Gabapentin 600mg
Arm Description
Outcomes
Primary Outcome Measures
Pain score by visual analogue scale (VAS) on movement at 24 hours postoperatively
Secondary Outcome Measures
Pain at rest and on movement by VAS, and maternal satisfaction at 6, 12, 24 & 48 hours postoperatively
Opioid consumption at 6, 12, 24 & 48 hours postoperatively
Assessment of sedation, pruritis, nausea, vomiting and dizziness on a 4-point scale (absent, mild, moderate, severe) and document treatment if required
Time to first maternal request for supplemental analgesia
Presence of pain 3 months postoperatively
Neonatal information: Apgar scores, arterial cord blood gases, need for neonatal intensive care unit (NICU) admission
Full Information
NCT ID
NCT01094925
First Posted
March 25, 2010
Last Updated
February 22, 2011
Sponsor
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01094925
Brief Title
The Effectiveness of Gabapentin for Post-operative Pain Following Cesarean Section
Official Title
The Effectiveness of a Pre-operative Single Dose Administration of Gabapentin for Management of Post-operative Pain Following Cesarean Section: a Randomised, Double-blind, Placebo-controlled, Dose-finding Study
Study Type
Interventional
2. Study Status
Record Verification Date
February 2011
Overall Recruitment Status
Completed
Study Start Date
April 2010 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
February 2011 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Gabapentin has been very effective at treating pain after knee and hip operations, hysterectomies, and many other types of operations. A previous study at the investigators' hospital found that a single pre-operative dose of 600mg gabapentin produced a significant reduction in pain after caesarean section. However, 19% complained of sedation. The purpose of this study is to see whether a reduced dose of gabapentin will produce a similar improvement in pain scores while avoiding adverse effects such as sedation or dizziness. The objective of this study is to compare the efficacy of a single pre-operative oral dose of gabapentin 300mg, versus 600mg and placebo in women undergoing Cesarean section. The investigators' hypothesis is that gabapentin 300mg will result in decreased pain scores similar to gabapentin 600mg, but with reduced side effects.
Detailed Description
Post-operative pain is the greatest fear of women who undergo Cesarean section, and despite current analgesic regimens, this pain can be severe, impeding the mother's recovery and her ability to bond with and breastfeed her new infant. Opioids are the mainstay of treatment currently, and, although effective, these drugs have significant adverse effects, including sedation, nausea, vomiting and constipation. Non-steroidal anti-inflammatory drugs (NSAIDs) can reduce opioid consumption, but also have side effects, and are contra-indicated in a significant number of patients. Therefore there remains considerable scope to improve post-Cesarean analgesia.
It has been shown that severe acute post-operative pain after Cesarean section increases the risk of developing chronic pain and post-partum depression. A recent study showed that up to 18% of women have persistent pain after Cesarean section, and that severe acute post-operative pain is a significant risk factor.
Gabapentin is used widely to treat chronic pain, and has been demonstrated to be effective at treating acute post-operative pain following a variety of surgical procedures, with significant reductions in opioid consumption. Side effects are uncommon; the most likely are dizziness and sedation. Gabapentin does cross the placenta and into breast milk, but there is no evidence of adverse maternal or neonatal effects in women taking gabapentin during pregnancy. Gabapentin has been used successfully to treat pain in neonates.
A recent study at Mount Sinai Hospital compared a single pre-operative dose of 600mg gabapentin versus placebo in women undergoing Cesarean section. Women in the gabapentin group reported significantly improved pain scores on movement up to 48 hours after surgery. Side effects were similar in both groups apart from an increase in somnolence in the gabapentin group.
The objective of this study is to compare the efficacy of a single pre-operative oral dose of gabapentin 300mg, versus 600mg and placebo in women undergoing Cesarean section. Our hypothesis is that gabapentin 300mg will result in decreased pain scores similar to gabapentin 600mg, but with reduced side effects. We have designed a randomized, double-blind, placebo-controlled study which will aim to answer these questions. Aside from the administration of gabapentin one hour prior to surgery, there are no other changes to the standard protocol of anaesthetic care. Women will be followed up for 48 hours after surgery for assessment of pain scores and overall satisfaction. A further follow-up at three months will determine the incidence of chronic pain.
Few studies have examined the incidence of chronic pain following Cesarean section, and none have examined the impact of pre-emptive analgesia using gabapentin on the incidence of chronic pain following Cesarean section. As the rate of Cesarean section continues to increase, and there remain significant problems with current analgesic regimens, the use of gabapentin, a drug with proven effectiveness in post-surgical pain and with limited side effects, has the potential to considerably improve acute and chronic post-Cesarean pain, and lead to a widespread change in clinical practice.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain
Keywords
Cesarean section, Gabapentin
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
126 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Gabapentin 300mg
Arm Type
Active Comparator
Arm Title
Gabapentin 600mg
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
lactose
Intervention Description
Single oral dose
Intervention Type
Drug
Intervention Name(s)
Gabapentin 300mg
Other Intervention Name(s)
Novo-gabapentin, Neurontin
Intervention Description
Single oral dose of 300mg gabapentin
Intervention Type
Drug
Intervention Name(s)
Gabapentin 600mg
Other Intervention Name(s)
Novo-gabapentin, Neurontin
Intervention Description
Single oral dose of 600mg gabapentin
Primary Outcome Measure Information:
Title
Pain score by visual analogue scale (VAS) on movement at 24 hours postoperatively
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Pain at rest and on movement by VAS, and maternal satisfaction at 6, 12, 24 & 48 hours postoperatively
Time Frame
48 hours
Title
Opioid consumption at 6, 12, 24 & 48 hours postoperatively
Time Frame
48 hours
Title
Assessment of sedation, pruritis, nausea, vomiting and dizziness on a 4-point scale (absent, mild, moderate, severe) and document treatment if required
Time Frame
48 hours
Title
Time to first maternal request for supplemental analgesia
Time Frame
48 hours
Title
Presence of pain 3 months postoperatively
Time Frame
3 months
Title
Neonatal information: Apgar scores, arterial cord blood gases, need for neonatal intensive care unit (NICU) admission
Time Frame
48 hours
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
18 years or older
full term singleton pregnancy
undergoing elective cesarean delivery
Exclusion Criteria:
Patients unable to communicate fluently in English
Patients with American Society of Anesthesiologists (ASA) classification of 3 or greater
Patients with history of epilepsy or chronic pain, or of use of anti-epileptic drugs or neuropathic analgesic drugs
Patients with a history of opioid or intravenous drug abuse
Patients with a known allergy or contra-indication to gabapentin, or to any other drugs used in this trial
Patients who have refused spinal anaesthesia, or those in whom it is contra-indicated
Patients with known congenital fetal abnormalities
Patients who have taken antacid medication in the previous 24 hours
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jose CA Carvalho, MD
Organizational Affiliation
MOUNT SINAI HOSPITAL
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mount Sinai Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M9W2S5
Country
Canada
12. IPD Sharing Statement
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The Effectiveness of Gabapentin for Post-operative Pain Following Cesarean Section
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