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NCT01993238 · ClinicalTrials.gov registry record · NA

Evaluation of Procedural Analgesia for Liposonix Treatment

A NA study of Body Contouring, sponsored by Solta Medical.

Completed
Registry status
NA
Development phase
11
Enrollment target
1
Study location

NCT01993238 is a NA study of Body Contouring that has completed, run by Solta Medical. The registered enrollment target is 11 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT01993238, a NA study of Body Contouring, has completed, sponsored by Solta Medical.

COMPLETED
Registry status
NA
Development phase
11 participants
Enrollment target
1
Study location

Study Summary

The objectives of this study are to evaluate the safety and effectiveness of procedural analgesia for improvements in tolerability of treatment with the Liposonix System.

Conditions Studied

Interventions

  • DEVICE Liposonix System (Model 2)
  • DRUG Pre-treatment analgesia

Study Locations (1)

California

  • Solta Medical Aesthetic Center - Hayward

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2013-11
Est. Completion 2014-01
Phase NA

Sponsor

Solta Medical

4 total trials

What the Registry Record Tells You About NCT01993238

The ClinicalTrials.gov registry entry for NCT01993238 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Solta Medical, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Body Contouring appearing as the primary indexed condition, and to 2 interventions - of which Liposonix System (Model 2) is the first listed.

NCT01993238 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT01993238 about?

NCT01993238 is a clinical study titled "Evaluation of Procedural Analgesia for Liposonix Treatment". The objectives of this study are to evaluate the safety and effectiveness of procedural analgesia for improvements in tolerability of treatment with the Liposonix System.

What is the current status of trial NCT01993238?

This trial is currently completed. It is a NA study. The enrollment target is 11 participants. The study started on 2013-11. Estimated completion is 2014-01.

What conditions does trial NCT01993238 study?

This clinical trial studies the following conditions: Body Contouring.

What interventions are being tested in trial NCT01993238?

The interventions under investigation include: Liposonix System (Model 2) (DEVICE), Pre-treatment analgesia (DRUG).

Who is sponsoring clinical trial NCT01993238?

This trial is sponsored by Solta Medical, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01993238 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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