Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02312739 · ClinicalTrials.gov registry record · NA
Nitrous Oxide for Pain Management During In-office Transcervical Sterilization
A NA study of Contraception and Inhalation of Nitrous Oxide, sponsored by University of New Mexi.
- Completed
- Registry status
- NA
- Development phase
- 72
- Enrollment target
- 1
- Study location
NCT02312739 is a NA study of Contraception and Inhalation of Nitrous Oxide that has completed, run by University of New Mexi. The registered enrollment target is 72 participants, below the 454-participant average among 72 other Contraception trials with a reported enrollment target (84% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02312739, a NA study of Contraception and Inhalation of Nitrous Oxide, has completed, sponsored by University of New Mexi.
- COMPLETED
- Registry status
- NA
- Development phase
- 72 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a randomized, double blind study that aims to measure the difference in maximum pain experienced during in-office transcervical sterilization (Essure®) for women receiving either inhaled nitrous oxide or standard oral analgesia (Vicodin and Lorazepam) with inhaled oxygen. The investigators hypothesize that inhaled nitrous oxide will reduce the pain experienced more than standard oral medications in women undergoing in-office transcervical sterilization.
Conditions Studied
Interventions
- OTHER Oxygen
- PROCEDURE In-office Transcervical Sterilization (Essure®)
- DRUG Standard Oral pain medications
- DRUG Intramuscular Ketorolac
- DRUG Placebo pills
Study Locations (1)
New Mexico
- UNM Center for Reproductive Health - Albuquerque
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2014-02 |
| Est. Completion | 2015-03 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02312739
The ClinicalTrials.gov registry entry for NCT02312739 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 454-participant average among 72 other Contraception trials with a reported enrollment target (84% lower). The listed sponsor is University of New Mexi, which has 76 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Contraception appearing as the primary indexed condition, and to 5 interventions - of which Oxygen is the first listed.
NCT02312739 reports 1 study location spanning 1 distinct geographic area - top geographies include New Mexico.
Frequently Asked Questions
What is clinical trial NCT02312739 about?
NCT02312739 is a clinical study titled "Nitrous Oxide for Pain Management During In-office Transcervical Sterilization". This is a randomized, double blind study that aims to measure the difference in maximum pain experienced during in-office transcervical sterilization (Essure®) for women receiving either inhaled nitrous oxide or standard oral analgesia (Vicodin and Lorazepam) with inhaled oxygen. The investigators ...
What is the current status of trial NCT02312739?
This trial is currently completed. It is a NA study. The enrollment target is 72 participants. The study started on 2014-02. Estimated completion is 2015-03.
What conditions does trial NCT02312739 study?
This clinical trial studies the following conditions: Contraception, Inhalation of Nitrous Oxide.
What interventions are being tested in trial NCT02312739?
The interventions under investigation include: Oxygen (OTHER), In-office Transcervical Sterilization (Essure®) (PROCEDURE), Standard Oral pain medications (DRUG), Intramuscular Ketorolac (DRUG), Placebo pills (DRUG).
Who is sponsoring clinical trial NCT02312739?
This trial is sponsored by University of New Mexi, which has 76 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02312739 being conducted?
This trial has 1 study location across New Mexico. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Contraception
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Patient-clinical Linkages to Improve Trust and Engagement in Postpartum Healthcare
RECRUITING · NA
-
Empathy Through Pain Control: Lidocaine Paracervical Block for IUD Placements
RECRUITING · NA
-
Hormonal Contraception Access Through Pharmacist Prescribing Implementation
RECRUITING · NA
-
Prospective Multi-Center Trial for FemBloc Permanent Birth Control
RECRUITING · NA
-
Contraceptive Efficacy Study of Ovaprene
RECRUITING · NA
-
Intervening on Women's Health for Rural Young Cancer Survivors
RECRUITING · NA
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.