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Phase 2 Study for the Treatment of Superficial Lipomas
NCT00608842 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this research is to compare the safety and effectiveness of 3 different concentrations of deoxycholic acid for injection against a placebo in the treatment of superficial lipomas.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Deoxycholic Acid Injection
Study Locations (7)
Alabama
- Gary D. Monheit, M.D. — Birmingham
California
- Stacy R. Smith — San Diego
Michigan
- Steven Grekin, D.O. — Warren
Nebraska
- Joel Schlessinger, M.D. — Omaha
New Jersey
- David J. Goldberg, M.D. — Westwood
New York
- Neil S. Sadick, M.D. — New York
Tennessee
- Michael H. Gold, M.D. — Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 62 participants |
| Start Date | 2007-11 |
| Est. Completion | 2010-01 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00608842
The ClinicalTrials.gov registry entry for NCT00608842 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 62 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Kythera Biopharmaceuticals, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Lipoma appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00608842 reports 7 study locations spanning 7 distinct geographic areas — top geographies include Alabama, California, Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00608842 about?
NCT00608842 is a clinical study titled "Phase 2 Study for the Treatment of Superficial Lipomas". The purpose of this research is to compare the safety and effectiveness of 3 different concentrations of deoxycholic acid for injection against a placebo in the treatment of superficial lipomas.
What is the current status of trial NCT00608842?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 62 participants. The study started on 2007-11. Estimated completion is 2010-01.
What conditions does trial NCT00608842 study?
This clinical trial studies the following conditions: Lipoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00608842?
The interventions under investigation include: Placebo (DRUG), Deoxycholic Acid Injection (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00608842?
This trial is sponsored by Kythera Biopharmaceuticals, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00608842 being conducted?
This trial has 7 study locations across Alabama, California, Michigan, Nebraska, New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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