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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: Clinical Trial NA study, sponsored by Planned Parenthood League of Massachusetts.
NCT00337792 is a NA study that was terminated before completion, run by Planned Parenthood League of Massachusetts. The registered enrollment target is 132 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.
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 |
Why NCT00337792 stopped before completion
NCT00337792 is an interventional study that assigns participants to a tested intervention. The registered 132 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).
The record links to 0 conditions, and to 1 intervention - of which oxycodone + lorazepam versus fentanyl + midazolam is the first listed.
NCT00337792 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00337792's enrollment target sits among peer trials
132 729th of 2000 higher than 1,269 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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