Comparing Sedara to Butorphanol in Early Labor
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Status
Sponsors
West Penn Allegheny Health System
CLINICAL TRIAL: NCT01636999
BioSeek: nct01636999
Keywords
Abstract
Nitrous oxide (N2O) has been used for the treatment of labor pains for over 150 years. The longevity of its use in clinical practice can be attributed to its excellent safety profile, ease of administration, and familiarity of use among health-care providers. Sedara is a self-administered 50% N2O, 50% oxygen gas mixture with pain relieving and anxiety reducing properties recently available for use in the United States (US) to treat various painful clnical situations, including labor pains.
In the US, epidural or intravenous administration of narcotic medications is one of the most common and frequently requested treatments for patients experiencing labor pains. Although generally considered safe, complications are common with epidurals, including fetal distress, low blood pressure in the mother, respiratory distress, and headache. In our hospital system, the use of the synthetic intravenous painkiller, Butorphanol, is a mainstay of treatment for labor pains. It too can have undesirable side effects in the mother, including low blood pressure and breathing problems.
Because Sedara has until recently been unavailable in the US, studies comparing its efficacy with other agents for labor pain have been confined to Europe, predominantly in the United Kingdom. Several studies have investigated the efficacy of Sedara versus inhalation and intravenous anesthetics in various countries. We have obtained several Sedara devices for use in the West Penn Allegheny Health System (WPAHS) Department of Anesthesiology and would like to examine its efficacy in our target population of women experiencing pain during early labor.
Hypothesis - Sedara will provide equivalent or superior pain relief among term, adult parturients in early labor (less than 5cm cervical dilation) compared to intravenous butorphanol.
Primary aim - Compare Sedara versus butorphanol in a single-blinded randomized trial with the main outcome measure being reduction in labor pains at various time intervals.
Our findings may be significant in terms of improving safety and efficacy of pain relief among women experienceing labor pains. Given that Sedara has not been previously studied in the US, the results may influence current obstetrical and pain management practices.
Dates
| Last Verified: | 06/30/2012 |
| First Submitted: | 07/05/2012 |
| Estimated Enrollment Submitted: | 07/08/2012 |
| First Posted: | 07/09/2012 |
| Last Update Submitted: | 07/08/2012 |
| Last Update Posted: | 07/09/2012 |
| Actual Study Start Date: | 08/31/2012 |
| Estimated Primary Completion Date: | 08/31/2014 |
| Estimated Study Completion Date: | 08/31/2014 |
Condition or disease
Labor Pain
Intervention/treatment
Drug: Butorphanol
Phase
-
Arm Groups
| Arm | Intervention/treatment |
|---|---|
| Experimental: Butorphanol The main study arm will be examining how well a 50% Nitrous Oxide/50% Oxygen gas mixture is in reducing labor pains in term labor patients with less than 5 cm cervical dilation, compared to 2mg of Butorphanol (a common synthetic opiod used for labor pains in this setting). | Drug: Butorphanol The gas mixture is provided via the Sedara portable gas delivery system. This system is equipped with a non-rebreather mask which the patient holds over their mouth and nose. The delivery of the gas is only triggered by the patient's spontaneous breath. The gas machine will be provided to the patient to use as much as they like during the 60 minutes data collection period. The only dose which the machine allows to be administered is 50% Nitrous Oxide/50% oxygen. |
Eligibility Criteria
| Ages Eligible for Study | 18 Years To 18 Years |
| Sexes Eligible for Study | Female |
| Accepts Healthy Volunteers | Yes |
| Criteria | Inclusion Criteria: - Female - 18 years of age or older - Presents in active labor - Full term pregnancy (at least 37 and up to 42 weeks gestation) - Less than 5 cm cervical dilation on exam Exclusion Criteria: - Patients who have received prior regional or opioid analgesia - Patients who have taken oral analgesics (narcotic or non-steroidal anti inflammatory drugs) within 6 hours prior to presentation |
Outcome
Primary Outcome Measures
1. Pain relief [60 minutes]
The primary outcome measure of pain relief will be measured using a 100mm visual analog scale (VAS) immediately prior to administration of the test medication (either Sedara or butorphanol) and again at 5, 15, 30 and 60 minutes following the medication start time.
Secondary Outcome Measures
1. Nausea, Sedation, Satisfaction [60 minutes]
Secondary outcome measures collected include maternal reported level nausea, sedation, and overall satisfaction with analgesia using the Visual Analog Scores Scale at 0, 5, 15, 30 and 60 minutes.
