Study to Evaluate Recovery From Postoperative Pain After Sleep Apnea Surgery
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00380458|
Recruitment Status : Withdrawn (No patients enrolled. Study did not start.)
First Posted : September 26, 2006
Last Update Posted : August 26, 2015
|Condition or disease||Intervention/treatment||Phase|
|Sleep Apnea, Obstructive||Device: Coblation (radiofrequency-based device)||Phase 4|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||0 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||Prospective, Randomized, Controlled Clinical Trial to Evaluate Recovery From Post-operative Pain in Adults After Sleep Apnea Surgery Using a Coblation Device Compared to Electrocautery|
- Number of days to cessation of narcotic pain medication use during the 21-day post-treatment period.
- Number of days to pain resolution as measured using a visual analogue scale during the 21-day post-treatment period.
- Analysis of timing of self-administration of medication during the 21-day post-treatment period
- Analysis of daily pain intensity using a visual analogue scale during the 21-day post-treatment period.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00380458
|United States, Minnesota|
|Mayo Clinic Rochester|
|Rochester, Minnesota, United States, 55905|
|Principal Investigator:||John Bitner, MD|