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NCT00337792 · ClinicalTrials.gov registry record · NA
Comparing the Effectiveness of Oral Versus Intravenous Pain Medicine for Suction Curettage (D&C)
A NA study, sponsored by Planned Parenthood League of Massachusetts.
- Terminated
- Registry status
- NA
- Development phase
- 132
- Enrollment target
NCT00337792 is a NA study that was terminated before completion, run by Planned Parenthood League of Massachusetts. The registered enrollment target is 132 participants.
The verdict
NCT00337792, a NA study, was terminated before completion, sponsored by Planned Parenthood League of Massachusetts.
- TERMINATED
- Registry status
- NA
- Development phase
- 132 participants
- Enrollment target
Study Summary
The main objective of this study is to determine the equivalency of oral conscious sedation and intravenous conscious sedation for first trimester surgical abortion. We hypothesize that oral conscious sedation will be equivalent to intravenous conscious sedation for pain control. Additional objectives include describing subject satisfaction with each method of pain control and characteristics of each method such as side effect profile, recovery room time, and postoperative pain.
Interventions
- DRUG oxycodone + lorazepam versus fentanyl + midazolam
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 132 participants |
| Start Date | 2006-06 |
| Est. Completion | 2007-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00337792
The ClinicalTrials.gov registry entry for NCT00337792 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 132 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Planned Parenthood League of Massachusetts, which has 13 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which oxycodone + lorazepam versus fentanyl + midazolam is the first listed.
NCT00337792 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00337792 about?
NCT00337792 is a clinical study titled "Comparing the Effectiveness of Oral Versus Intravenous Pain Medicine for Suction Curettage (D&C)". The main objective of this study is to determine the equivalency of oral conscious sedation and intravenous conscious sedation for first trimester surgical abortion. We hypothesize that oral conscious sedation will be equivalent to intravenous conscious sedation for pain control. Additional objectiv...
What is the current status of trial NCT00337792?
This trial is currently terminated. It is a NA study. The enrollment target is 132 participants. The study started on 2006-06. Estimated completion is 2007-07.
What interventions are being tested in trial NCT00337792?
The interventions under investigation include: oxycodone + lorazepam versus fentanyl + midazolam (DRUG).
Who is sponsoring clinical trial NCT00337792?
This trial is sponsored by Planned Parenthood League of Massachusetts, which has 13 total clinical trials registered on ClinicalTrials.gov.
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