search
Back to results

ATT Compared With ATE in OSAS Children (RCT ATE/ATT)

Primary Purpose

Obstructive Sleep Apnea Syndrome in Children

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Adenotonsillectomy
Adenotonsillotomy
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 in Children focused on measuring Obstructive sleep apnea syndrome, Children, Polysomnography, Surgery, Coblation, Tonsils, Tonsillectomy

Eligibility Criteria

2 Years - 6 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children aged 2-6 years
  • Clinical symptoms of OSAS (apneas, snoring, disturbed sleep)
  • Tonsil size 3-4 with the Brodsky scale (obstructing at least 50% of the oro-pharyngeal space)
  • Apnea-Hypopnea Index (AHI) 5-30 (moderate- severe OSA)

Exclusion Criteria:

  • Clinical signs of craniofacial anomalies or neuromuscular disorders
  • Obesity
  • Earlier having had surgery of tonsils or adenoid
  • Bleeding disorder
  • Cardiopulmonary disorder

Sites / Locations

  • Karolinska University Hospital, ORL dep

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Adenotonsillectomy

Adenotonsillotomy

Arm Description

Total removal of tonsils and adenoids with cold steel

Partial removal of tonsils with coblation and total removal of adenoids with cold steel

Outcomes

Primary Outcome Measures

Changes in polysomnographic parameter AHI (Apnea Hypopnea Index)
AHI; the number of apneas and hypopneas per sleep hour, is measured through polysomnography before and after surgery.

Secondary Outcome Measures

Changes in quality of life questionnaires (OSA18 and SDQ)
Parents answering to quality of life-questionnaire OSA18 and SDQ (Strengths and Difficulties Questionnaire) before and after surgical intervention

Full Information

First Posted
August 21, 2012
Last Updated
March 9, 2023
Sponsor
Karolinska University Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT01676181
Brief Title
ATT Compared With ATE in OSAS Children
Acronym
RCT ATE/ATT
Official Title
Randomised Surgical Intervention Study Between Adenotonsillectomy and Adenotonsillotomy in Children With Obstructive Sleep Apnea Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
November 2011 (undefined)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
March 2017 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Non-inferiority hypothesis; adenotonsillotomy is equally good as adenotonsillectomy in treating obstructive sleep apnea syndrome (OSAS) in children after one, three and ten years.
Detailed Description
Background: Children with obstructive sleep apnea syndrome (OSAS) have apneas and disturbed sleep, which causes daytime symptoms such as neurobehavioral problems. OSAS is a significant cause of morbidity among children with an incidence of 1-3%, and a peak prevalence at 2-5 years of age. If left untreated it can cause severe complications including failure to thrive, cardiovascular complications, metabolic conditions and neurobehavioral disturbances (eg hyperactivity, inattention). Golden standard to diagnose OSA in children is full-night polysomnography (PSG) at a sleep laboratory including EEG, EOG, EMG, video-audiometry and respiratory recordings. At the Department of Otorhinolaryngology at Karolinska University Hospital, we have a sleep laboratory performing in-lab full-night polysomnography. The cause of OSAS in children is usually adenotonsillar hypertrophy, and the treatment of choice is surgical removal of tonsils and adenoid. Traditionally total adenotonsillectomy (ATE) has been performed, but in the last decade an alternative surgical method with partial adenotonsillotomy (ATT) is developed, where only the medial portion of the tonsil is removed. The newer method ATT is not fully evaluated in comparison with traditional ATE. There are studies comparing evaluating post-operative pain and bleeding showing a slight advantage for the TT-method. Very few studies are performed using objectively measured PSG-parameters to evaluate the effect of surgery on the sleep fragmentation and the sleep apneas. There is a need for such studies in the field of surgical treatment of pediatric OSA. This was also stated in a Cochrane database review from 2009, in which the conclusion was that there is a need for high quality randomised controlled trials to be carried out investigating the efficacy of surgical treatment of OSA in children. This makes this study important and of high clinical interest. Aims: To increase the knowledge of pediatric OSA and its treatment and to optimize the surgical treatment for children with OSA. To through a blinded randomized controlled trial compare the efficacy of ATT and ATE in treating OSA in children, including long-term follow-up after one, three and ten years. To evaluate postoperative pain after ATE and ATT. To evaluate quality of life after ATE and ATT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnea Syndrome in Children
Keywords
Obstructive sleep apnea syndrome, Children, Polysomnography, Surgery, Coblation, Tonsils, Tonsillectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
79 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Adenotonsillectomy
Arm Type
Active Comparator
Arm Description
Total removal of tonsils and adenoids with cold steel
Arm Title
Adenotonsillotomy
Arm Type
Active Comparator
Arm Description
Partial removal of tonsils with coblation and total removal of adenoids with cold steel
Intervention Type
Procedure
Intervention Name(s)
Adenotonsillectomy
Intervention Description
Total removal of tonsils and adenoid tissue with cold-steel
Intervention Type
Procedure
Intervention Name(s)
Adenotonsillotomy
Intervention Description
Partial removal of tonsils with coblation and total removal of adenoids with cold steel
Primary Outcome Measure Information:
Title
Changes in polysomnographic parameter AHI (Apnea Hypopnea Index)
Description
AHI; the number of apneas and hypopneas per sleep hour, is measured through polysomnography before and after surgery.
Time Frame
One, three and ten years
Secondary Outcome Measure Information:
Title
Changes in quality of life questionnaires (OSA18 and SDQ)
Description
Parents answering to quality of life-questionnaire OSA18 and SDQ (Strengths and Difficulties Questionnaire) before and after surgical intervention
Time Frame
One, three and ten Years
Other Pre-specified Outcome Measures:
Title
Per- and postoperative bleeding
Description
The two groups (ATT and ATE) will be compared concerning per- and postoperative bleeding.
Time Frame
One year
Title
changes in polysomnographic parameters other than AHI
Description
Polysomnograhic parameters, for example; the oxygen desaturation index (ODI), lowest oxygen saturation, the respiratory disturbance index (RDI), AHI in REM, total sleep time, time in REM, deep sleep, supine position etc.
Time Frame
one, three and ten years
Title
Differences in postoperative pain
Description
The two groups will be compared with questionnaires and consumption of analgetics concerning the degree of postoperative pain.
Time Frame
One year
Title
Number of patients who need reoperations
Description
The patient may need reoperations, either because of postoperative bleeding or because the tonsils have regrowth
Time Frame
One, three and ten years
Title
Abnormalities in DNA analysis of blood and tonsil tissue
Description
Blood and tissue samples will be frozen for future analysis of DNA. We have not yet decided which method we will use. There are other studies suggesting abnormalities in certain enzymes in children with tonsillar hypertrophy
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children aged 2-6 years Clinical symptoms of OSAS (apneas, snoring, disturbed sleep) Tonsil size 3-4 with the Brodsky scale (obstructing at least 50% of the oro-pharyngeal space) Apnea-Hypopnea Index (AHI) 5-30 (moderate- severe OSA) Exclusion Criteria: Clinical signs of craniofacial anomalies or neuromuscular disorders Obesity Earlier having had surgery of tonsils or adenoid Bleeding disorder Cardiopulmonary disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Danielle Friberg, MD, PhD
Organizational Affiliation
Karolinska University Hospital, ORL dep
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska University Hospital, ORL dep
City
Stockholm
ZIP/Postal Code
141 86
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
32347984
Citation
Blackshaw H, Springford LR, Zhang LY, Wang B, Venekamp RP, Schilder AG. Tonsillectomy versus tonsillotomy for obstructive sleep-disordered breathing in children. Cochrane Database Syst Rev. 2020 Apr 29;4(4):CD011365. doi: 10.1002/14651858.CD011365.pub2.
Results Reference
derived
PubMed Identifier
31377901
Citation
Borgstrom A, Nerfeldt P, Friberg D. Postoperative pain and bleeding after adenotonsillectomy versus adenotonsillotomy in pediatric obstructive sleep apnea: an RCT. Eur Arch Otorhinolaryngol. 2019 Nov;276(11):3231-3238. doi: 10.1007/s00405-019-05571-w. Epub 2019 Aug 3.
Results Reference
derived

Learn more about this trial

ATT Compared With ATE in OSAS Children

We'll reach out to this number within 24 hrs