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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02522247
Other study ID # 2015/755-31/2B
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated

Study information

Verified date March 2023
Source Karolinska University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare the effect of uvulopalatoplasty with no treatment in treating adult OSA.


Description:

Two arms: the intervention group undergo uvulopalatoplasty one month after baseline polysomnography (PSG1) and a PSG2 6 months after surgery . The control group perform PSG 1 and are then waiting 6 months, thereafter undergo PSG2, then surgery and PSG3 6 months after surgery. All patients are followed for four years with PSG. Patients fill in questionnaires at PSG sessions, and blood pressure control the morning after.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date December 10, 2015
Accepts healthy volunteers No
Gender All
Age group 30 Years to 65 Years
Eligibility Inclusion Criteria: - AHI of 15 or more - Friedmans stage I+II - Tonsil size 0-1 - BMI<34 - ESS värde >7 - Failed treatment with CPAP and mandibular device Exclusion Criteria: - Severe cardiovascular or neurological disease - ASA IV - Not interested in surgical treatment

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
UPP
surgery with cold steel in general anesthesia

Locations

Country Name City State
Sweden Orl dep, Karolinska University Hospital Stockholm

Sponsors (1)

Lead Sponsor Collaborator
Karolinska University Hospital

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Other Polysomnography: changes of AHI between baseline and 4 years postoperatively The control group is operated with uvulopalatoplasty (delayed surgery) after 6 months waiting. This outcome is for all 100 patients. 4 years
Other Questionnaire: changes of daytime sleepiness between baseline and 4 years postoperatively The control group is operated with uvulopalatoplasty (delayed surgery) after 6 months waiting. This outcome is for all 100 patients. 4 years
Other Questionnaire: changes of general health between baseline and after 4 years postoperatively The control group is operated with uvulopalatoplasty (delayed surgery) after 6 months waiting. This outcome is for all 100 patients. 4 years
Other Postoperative bleeding complications postop bleeding in milliliter 6 months
Other Postoperative days at hospital report number of days at hospital postop 6 months
Primary Polysomnography: group differences in changes of apnea-hypopnea index (AHI) compare the two groups of changes in number of apneas and hypopneas per sleep hour measured with inlab polysomnography, between baseline and follow-up 6 months
Secondary Questionnaire: group differences in changes of daytime sleepiness using validated questionnaire Epworth sleepiness scale measure changes between baseline and follow-up and compare the differences between groups 6 months
Secondary Questionnaire: group differences in changes of general health using validated question 6 months
Secondary Blood pressure: group differences in changes of blood pressure 6 months
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