Inhaled Nitrous Oxide and Labor Analgesia
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| ClinicalTrials.gov Identifier: NCT01738672 |
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Recruitment Status :
Terminated
First Posted : November 30, 2012
Results First Posted : November 21, 2017
Last Update Posted : November 21, 2017
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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.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Labor Pain | Drug: Inhaled nitrous oxide | Phase 2 |
Show detailed description
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 16 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | Inhaled Nitrous Oxide and Labor Analgesia |
| Study Start Date : | February 2012 |
| Actual Primary Completion Date : | October 2013 |
| Actual Study Completion Date : | October 2013 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Nitrous Oxide
Parturients who request labor analgesia will be offered inhaled nitrous oxide for labor analgesia.
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Drug: Inhaled nitrous oxide
Administration of nitrous oxide for labor analgesia
Other Names:
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- Labor Pain [ Time Frame: At baseline, and at 1 hour after initiation of nitrous oxide ]Participant reported pain score, using a numerical rating scale (NRS) ranging from no pain (0) to severe pain (10).
- Anxiety [ Time Frame: At baseline, and at 1 hour after initiation of nitrous oxide ]Participant reported anxiety score, using a numerical rating scale (NRS) ranging from no anxiety (0) to severe anxiety (10).
- Nausea [ Time Frame: At baseline, and at 1 hour after initiation of nitrous oxide ]Participant reported nausea score, using a numerical rating scale (NRS) ranging from no nausea (0) to severe nausea (10).
- Emesis [ Time Frame: During administration of nitrous oxide ]Participant reported emesis (yes or no).
- Participant Satisfaction [ Time Frame: 24 hours after delivery ]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).
- Crossover To Epidural [ Time Frame: Initiation of nitrous oxide to completion of delivery. ]Participants crossing over from nitrous oxide to epidural.
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| Ages Eligible for Study: | 14 Years and older (Child, Adult, Older Adult) |
| Sexes Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01738672
| United States, Pennsylvania | |
| Magee-Womens Hospital | |
| Pittsburgh, Pennsylvania, United States, 15213 | |
| Principal Investigator: | Ya'aqov Abrams, MD | University of Pittsburgh |
| Responsible Party: | Ya'aqov Abrams, Assistant Professor, University of Pittsburgh |
| ClinicalTrials.gov Identifier: | NCT01738672 |
| Other Study ID Numbers: |
PRO11090221 |
| First Posted: | November 30, 2012 Key Record Dates |
| Results First Posted: | November 21, 2017 |
| Last Update Posted: | November 21, 2017 |
| Last Verified: | October 2017 |
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Nitrous oxide labor and delivery analgesia |
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Labor Pain Pain Neurologic Manifestations Nitrous Oxide Entonox Anesthetics, Inhalation Anesthetics, General Anesthetics |
Central Nervous System Depressants Physiological Effects of Drugs Analgesics, Non-Narcotic Analgesics Sensory System Agents Peripheral Nervous System Agents Anesthetics, Combined |

