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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03553342
Other study ID # THYRCOR
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date September 11, 2018
Est. completion date January 11, 2022

Study information

Verified date January 2021
Source Poitiers University Hospital
Contact Xavier DUFOUR, Pr
Phone 0549444328
Email xavier.dufour@chu-poitiers.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Thyroidectomy is a common surgical procedure in France. Recurrent paralysis is one of the main complications. Oral corticosteroid therapy are frequently used at a dosage of 1mg/kg for seven days, in case of recurrent paralysis to obtain remobilization as early as possible. The main objective is to evaluate the efficacy of oral corticosteroid therapy in remobilization of vocal cords at seven days in patients with unilateral recurrent paralysis after thyroidectomy.


Recruitment information / eligibility

Status Recruiting
Enrollment 156
Est. completion date January 11, 2022
Est. primary completion date September 11, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients scheduled for simple total thyroidectomy or lobo-isthmectomy - Patients over eighteen years old - Free subject, whitout tutorship or curatorship or subordination - Informed consent and signed by the patient after clear and fair information about the study. Exclusion Criteria: - Patients operated on a total thyroidectomy with médiastino-recurrent dissection for cancer etiology - Patients with preoperative recurrent paralysis - Patients with hypersensitivity to prednisolone or any of the excipients. - Patients with contraindication to use Solupred - Patients with anti-inflammatory of acetylsalicylic acid - Patient with evolving virosis (hepatitis, herpes, chicken pox, zoster)

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Corticoids
Patients will receive corticosteroids therapy: 1mg/kg of prednisolone daily for seven days.
Other:
Placebo
Patients will receive placebo for seven days.

Locations

Country Name City State
France Chu Poitiers Poitiers

Sponsors (1)

Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluate the efficacy of oral corticosteroid in remobilization of vocal cords at seven days for patients with unilateral recurrent laryngeal nerve palsy after thyroidectomy evaluated by naso fibroscope inspection Seven days