Thyroidectomy Clinical Trial
— DEGLUTHYROfficial title:
Interest of Cryotherapy or Cortisone Aerosol Therapy in Early Post-operative Swallowing Disorders Following Total Thyroidectomy
Verified date | December 2018 |
Source | Centre Hospitalier Universitaire Dijon |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The scientific interest of this study is to improve post-operative comfort in patients after thyroid surgery using simple, inexpensive techniques. The investigator expects that local applications of ice or cortisone aerosols will reduce swallowing discomfort and control post-operative pain (POP). The investigator hopes that local cryotherapy will decrease post-operative oedema (vasoconstriction) and the volume of liquid drained (action on the serous fluid at the site of the thyroidectomy).
Status | Completed |
Enrollment | 240 |
Est. completion date | February 20, 2015 |
Est. primary completion date | February 20, 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients about to undergo total thyroidectomy by cervicotomy - Single surgeon: Dr Osmak-Tizon Liliana - Patients who have provided written consent to take part in the research - Hospitalized in the endocrine surgery unit - Whose mental and physical state allows them to participate in the quantification of a symptom using a Visual Analogue Scale(VAS) Exclusion Criteria: - Patients under 18 or adults under guardianship - Patients about to undergo unilateral thyroid surgery (thyroid lobectomy) - Patient who have had parathyroid surgery - History of cervicotomy - Intolerance to, contra-indication for or allergy to any of the treatments tested. - Pregnant or breast-feeding women - Patients without national health insurance cover |
Country | Name | City | State |
---|---|---|---|
France | CHU Dijon Bourgogne | Dijon |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Universitaire Dijon |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Swallowing Impairment Score (SIS). | Evolution of the SIS from baseline (inclusion), to the end of the surgery and every day thereafter until discharge of the patient(up to 3 months) |
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