Labor Pain Clinical Trial
Official title:
Inhaled Nitrous Oxide and Labor Analgesia
Verified date | October 2017 |
Source | University of Pittsburgh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Hypothesis: The administration of nitrous oxide for labor analgesia will decrease the labor
epidural anesthesia rate by 15%.
Specific Aim: To determine if nitrous oxide can be an effective alternative technique for the
provision of labor analgesia at Magee-Womens Hospital.
Status | Terminated |
Enrollment | 16 |
Est. completion date | October 2013 |
Est. primary completion date | October 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 14 Years and older |
Eligibility |
Inclusion Criteria: - all women of childbearing age (including children aged 14 years and above)who are pregnant - parturients who request labor analgesia of family medicine investigators certified in the use of nitrous oxide for labor analgesia at Magee-Women's Hospital - informed verbal and written consent Exclusion Criteria: - coexisting medical conditions that are contraindications to the use of nitrous oxide (i.e. recent eye or ear surgery, history of Meniere's disease, history of vitamin B-12 deficiency) - history of severe nausea and vomiting - history of chronic pain - inability to hold a facemask - impairment of consciousness or intoxication at time of delivery - received intravenous opioids within two hours prior to initiation of nitrous oxide - impaired oxygenation (ex: lung cysts, pneumothorax, pulmonary hypertension, or pulmonary edema) with a room-air pulse oximetry reading less than 95% - hemodynamic instability - non-reassuring fetal heart rate tracing - inability to read, write and understand the English language enough to complete all survey questionnaires and pain assessment scales. |
Country | Name | City | State |
---|---|---|---|
United States | Magee-Womens Hospital | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Ya'aqov Abrams | University of Pittsburgh |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Anxiety | Participant reported anxiety score, using a numerical rating scale (NRS) ranging from no anxiety (0) to severe anxiety (10). | At baseline, and at 1 hour after initiation of nitrous oxide | |
Other | Nausea | Participant reported nausea score, using a numerical rating scale (NRS) ranging from no nausea (0) to severe nausea (10). | At baseline, and at 1 hour after initiation of nitrous oxide | |
Other | Emesis | Participant reported emesis (yes or no). | During administration of nitrous oxide | |
Other | Participant Satisfaction | Participant reported score of satisfaction with nitrous oxide for labor analgesia, using a numerical rating scale (NRS) ranging from completely dissatisfied (0) to completely satisfied (100). | 24 hours after delivery | |
Other | Crossover To Epidural | Participants crossing over from nitrous oxide to epidural. | Initiation of nitrous oxide to completion of delivery. | |
Primary | Labor Pain | Participant reported pain score, using a numerical rating scale (NRS) ranging from no pain (0) to severe pain (10). | At baseline, and at 1 hour after initiation of nitrous oxide |
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