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RCT of the Effect of Uvulopalatopharyngoplasty Compared to Expectancy in Patients With Obstructive Sleep Apnea (SKUP3)

Primary Purpose

Obstructive Sleep Apnea Syndrome

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Uvulopalatopharyngoplasty
Sponsored by
Karolinska University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obstructive Sleep Apnea Syndrome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

ApnéHypopnéIndex, AHI >14,9 Daytime sleepiness w Epworth sleepiness scale, ESS> 7 Sleepy during daytime 3-5 times per week or more BodyMassIndex, BMI < 36,0 Friedman staging system of tonsil size and tongue: i and II Patients w Friedman stage I and BMI < 30,0 could be directly included if patient positive and no contra-indications for surgery. All others should be failure of CPAP and MRD before inclusion.

Exclusion Criteria:

Other OSAS treatment during study, i.e., patient is clinically severely deteriorated.

Negative to surgery Night-shift worker Friedman stage III or IV Morbid obesity BMI >35,9 Severe psychological or neurological disease ASA class >3 Severe lung- or heart disease (not applicable for hypertension, nor stroke or MI more than after 2 years).

Insufficient knowledge in Swedish language (important for filling in questionnaires) Dangerous in traffic while driving Severe nasal congestion (can be included after successful treatment) Previous tonsillectomy

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Sites / Locations

  • ORL dep, Karolinska University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Uvulopalatopharyngoplasty

Control

Arm Description

One arm is Uvulopalatopharyngoplasty(intervention group of 32 patients), one arm is expectancy (control group of 33 patients). After six months the controls have delayed surgery and then both groups are followed for two years

After six months the controls have delayed surgery then are followed for 2 year

Outcomes

Primary Outcome Measures

Changes in apnea-hypopnea index
Apnea-hypopnea index (AHI) is the number of apneas or hypopneas per sleep hour. Polysomnography (PSG) is the Golden standard to use when measuring the AHI. PSG is the method we are using

Secondary Outcome Measures

Changes in Epworth sleepiness scale
Epworth sleepiness scale is a validated questionnaire. It consists of eight questions concerning the patients´ ability to fall asleep in different situations. The total sum is 24.

Full Information

First Posted
August 6, 2012
Last Updated
December 12, 2014
Sponsor
Karolinska University Hospital
Collaborators
Karolinska Institutet
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1. Study Identification

Unique Protocol Identification Number
NCT01659671
Brief Title
RCT of the Effect of Uvulopalatopharyngoplasty Compared to Expectancy in Patients With Obstructive Sleep Apnea
Acronym
SKUP3
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska University Hospital
Collaborators
Karolinska Institutet

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hypothesis:Pharyngeal surgery (UPPP) reduces significantly the nightly respiratory breathing pauses (apnoeas-hypopnoeas) and improves the daytime symptoms compared to expectancy for 6 months in patients with OSAS. Background: Obstructive sleep apnea syndrome (OSAS) is associated with an increased risk of poor sleep quality, excessive daytime sleepiness and prolonged reaction time, which can elevate the risk for traffic accidents. Increased morbidity and three to four times increased mortality in these patients are well documented, mainly in the cardiovascular field. Pharyngeal surgery, i.e. uvulopalatopharyngoplasty (UPPP) opens up the airway and was the predominant treatment for OSAS worldwide before continuous positive airway pressure (CPAP) devices became widely available in the 1990s. Since then, the main treatment for OSAS has been CPAP, but an increasing number of patients are also treated with mandibular retaining device (MRD). UPPP as treatment for OSAS has been performed for 30 years. The evidence-grade for the efficacy has so far been very low, and the side-effects and complication rate has raised the question whether there is a place for surgical treatment of OSAS. However, the compliance for CPAP and dental devices are quite low (50-60%), leaving a lot of patients untreated if surgery is not offered. RCT UPPP is still missing and called for.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnea Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
65 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Uvulopalatopharyngoplasty
Arm Type
Active Comparator
Arm Description
One arm is Uvulopalatopharyngoplasty(intervention group of 32 patients), one arm is expectancy (control group of 33 patients). After six months the controls have delayed surgery and then both groups are followed for two years
Arm Title
Control
Arm Type
Active Comparator
Arm Description
After six months the controls have delayed surgery then are followed for 2 year
Intervention Type
Procedure
Intervention Name(s)
Uvulopalatopharyngoplasty
Intervention Description
Uvulopalatopharyngoplasty: Resection of the soft palate 3 mm and tonsillectomy, amputation of the uvula to approx 1 cm, single sutures of the posterior pillar to the anterior pillar and of the soft palate.
Primary Outcome Measure Information:
Title
Changes in apnea-hypopnea index
Description
Apnea-hypopnea index (AHI) is the number of apneas or hypopneas per sleep hour. Polysomnography (PSG) is the Golden standard to use when measuring the AHI. PSG is the method we are using
Time Frame
6 months and 2 years
Secondary Outcome Measure Information:
Title
Changes in Epworth sleepiness scale
Description
Epworth sleepiness scale is a validated questionnaire. It consists of eight questions concerning the patients´ ability to fall asleep in different situations. The total sum is 24.
Time Frame
6 months and 2 years
Other Pre-specified Outcome Measures:
Title
Changes in Oxygen desaturation index
Description
Oxygen desaturation index (ODI) is the number of oxygen desaturations of 3 % or more per sleep hour.
Time Frame
6 months and 2 years
Title
changes in blood samples
Description
Hb, LPK, CRP, cortisol, TSH, T4, ASAT, ALAT, ALP, γ-GT, CDT, Leptin/ghrelin, fB-Glucose, f-insulin, HDL, LDL, Cholesterol, Triglycerides, TNF-α, IL-1, IL-6
Time Frame
6 months 2 years
Title
changes in score of SF 36 quality of life questionnaire
Description
QoL SF 36 validated questionnaire
Time Frame
6 months and 2 years
Title
changes in blood pressure
Description
systolic and diastolic morning pressure from arm
Time Frame
6 months and 2 years
Title
changes in vigilance
Description
modified Osler test
Time Frame
6 months and 2 years
Title
number of patients with serious complications from surgery
Time Frame
6 months
Title
number of patients with side-effects from surgery
Description
answers from a local questionnaire regaring pharyngeal side-effects
Time Frame
6 months and 2 years
Title
Changes in score of FOSQ questionnaire
Description
Validated questionnaire designed for patients with obstructive sleep apnea syndrome
Time Frame
6 months and 2 years
Title
identifying success factors for outcome of surgical intervention
Description
Correlate for example tonsil size and tongue position (stageing system) with changes in AHI
Time Frame
6 months 2 years
Title
changes in arousal index
Description
Polysomnographic results
Time Frame
6 months and 2 years
Title
changes in lowest oxygen saturation during sleep
Description
Polysomnographic results
Time Frame
6 months 2 years
Title
changes in ODI during REM sleep
Description
Polysomnographic results
Time Frame
6 months 2 years
Title
changes in ODI in supine position
Description
Polysomnographic results
Time Frame
6 months 2 years
Title
changes in time in supine position
Description
Polysomnographic results
Time Frame
6 months and 2 years
Title
changes in Body Mass Index
Time Frame
6 months and 2 years
Title
changes in RERA index
Description
Polysomnographic results, RERA are the respiratory effort related arousals during sleep
Time Frame
6 months and 2 years
Title
changes in mean length apneas and hypopneas
Description
Polysomnographic results
Time Frame
6 months and 2 years
Title
changes in AHI supine position
Description
Polysomnographic results
Time Frame
6 months 2 years
Title
changes in AHI in REM
Description
Polysomnographic results
Time Frame
6 months and 2 years
Title
changes in total sleep time
Description
Polysomnograåhic results
Time Frame
6 months and 2 years
Title
changes in RDI
Description
Polysomnographic results; RDI is the sum of AHI and RERA index
Time Frame
6 months and 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ApnéHypopnéIndex, AHI >14,9 Daytime sleepiness w Epworth sleepiness scale, ESS> 7 Sleepy during daytime 3-5 times per week or more BodyMassIndex, BMI < 36,0 Friedman staging system of tonsil size and tongue: i and II Patients w Friedman stage I and BMI < 30,0 could be directly included if patient positive and no contra-indications for surgery. All others should be failure of CPAP and MRD before inclusion. Exclusion Criteria: Other OSAS treatment during study, i.e., patient is clinically severely deteriorated. Negative to surgery Night-shift worker Friedman stage III or IV Morbid obesity BMI >35,9 Severe psychological or neurological disease ASA class >3 Severe lung- or heart disease (not applicable for hypertension, nor stroke or MI more than after 2 years). Insufficient knowledge in Swedish language (important for filling in questionnaires) Dangerous in traffic while driving Severe nasal congestion (can be included after successful treatment) Previous tonsillectomy -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Danielle K Friberg, MD, PhD, Associate professor
Organizational Affiliation
Karolinska University Hospital, Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
ORL dep, Karolinska University Hospital
City
Stockholm
ZIP/Postal Code
141 86
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
29099950
Citation
Joar S, Danielle F, Johan B, Arne L, Roberta N, Nanna B. Sleep Quality After Modified Uvulopalatopharyngoplasty: Results From the SKUP3 Randomized Controlled Trial. Sleep. 2018 Jan 1;41(1). doi: 10.1093/sleep/zsx180. Erratum In: Sleep. 2018 Nov 1;41(11):
Results Reference
derived
PubMed Identifier
28522085
Citation
Fehrm J, Friberg D, Bring J, Browaldh N. Blood pressure after modified uvulopalatopharyngoplasty: results from the SKUP3 randomized controlled trial. Sleep Med. 2017 Jun;34:156-161. doi: 10.1016/j.sleep.2017.02.030. Epub 2017 Apr 4.
Results Reference
derived
PubMed Identifier
26404729
Citation
Browaldh N, Bring J, Friberg D. SKUP(3) RCT; continuous study: Changes in sleepiness and quality of life after modified UPPP. Laryngoscope. 2016 Jun;126(6):1484-91. doi: 10.1002/lary.25642. Epub 2015 Sep 25.
Results Reference
derived
PubMed Identifier
23644225
Citation
Browaldh N, Nerfeldt P, Lysdahl M, Bring J, Friberg D. SKUP3 randomised controlled trial: polysomnographic results after uvulopalatopharyngoplasty in selected patients with obstructive sleep apnoea. Thorax. 2013 Sep;68(9):846-53. doi: 10.1136/thoraxjnl-2012-202610. Epub 2013 May 5.
Results Reference
derived

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RCT of the Effect of Uvulopalatopharyngoplasty Compared to Expectancy in Patients With Obstructive Sleep Apnea

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