Impact of thyroid surgery on sleep apnea in goiter patients
Effects of Thyroidectomy on Obstructive Sleep Apnea in Patients Suffering From Goiters
This study looks at how thyroid surgery affects sleep apnea in people with goiters to see if it helps them breathe better while sleeping.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 90 Years |
| Sex | All |
| Sponsor | Centre Hospitalier Universitaire Saint Pierre Academic / other |
| Locations | 1 site (Brussels) |
| Trial ID | NCT05391945 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the prevalence of obstructive sleep apnea (OSA) in patients with goiters who are scheduled for thyroidectomy. It will assess the role of thyroidectomy in resolving OSA in those who have pre-operative OSA and identify predictors for patients who may continue to experience OSA post-surgery. Patients will undergo home polysomnography and pulmonary function tests before and three months after the surgery to evaluate changes in their condition.
Who should consider this trial
Good fit: Ideal candidates are patients scheduled for thyroidectomy due to goiter.
Not a fit: Patients with previous cervical surgery, language barriers, or chest diseases that narrow the upper airways may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management of obstructive sleep apnea in patients with goiters, enhancing their quality of life.
How similar studies have performed: Previous reports have indicated that thyroidectomy can resolve OSA in some patients with goiters, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: °patients planned for thyroidectomy for goiter Exclusion Criteria: * previous cervical surgery/radiotherapy * language barrier * chest disease known to narrow upper airways
Where this trial is running
Brussels
- CHU Saint Pierre — Brussels, Belgium (Recruiting)
Study contacts
- Study coordinator: Marie Bruyneel, MD,PhD
- Email: marie.bruyneel@stpierre-bru.be
- Phone: +3225354219
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.