The Recovery Profiles After Robotic or Open Thyroidectomy
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Contacts and Locations
Study Contact
Study Contact
- Name: Yeji Lee, Pf
- Phone Number: 82317877499
- Email: ladydaisy82@naver.com
Study Locations
-
-
Gyeonggi-do
-
Seongnam-si, Gyeonggi-do, Korea, Republic of, 463-707
- Recruiting
- Ah-young Oh
-
Contact:
- Yeji Lee, Pf
- Phone Number: 82317877499
- Email: ladydaisy82@naver.com
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients undergoing robotic thyroidectomy or open conventional thyroidectomy
- Adults 19 to 70 years of age
- American Society of Anesthesiologists Physical grade 1-2
Exclusion Criteria:
- Patients who underwent surgery on the neck and in the laryngeal area before
- Patients who do not understand or can not express pain scale
- Patients with sore throat and cough before surgery
- If intubation is difficult or repeated intubation is performed
- Patients who are using opioids or analgesics as chronic agents.
Study Plan
How is the study designed?
Design Details
Number of groups / cohorts
Cohorts and Interventions
Group / CohortGroup / Cohort |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
robotic thyroidectomy group
|
In robotic thyroidectomy group, patients are received surgery using robotic system.
In open thyroidectomy group, patients are received conventional open surgery.
|
|
open thyroidectomy group
|
In robotic thyroidectomy group, patients are received surgery using robotic system.
In open thyroidectomy group, patients are received conventional open surgery.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
postoperative sore throat
Time Frame: postoperative 1 hour
|
none, mild, moderate, severe
|
postoperative 1 hour
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Study Start
Primary Completion (ANTICIPATED)
Primary Completion
Study Completion (ANTICIPATED)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (ACTUAL)
First Posted
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- B-1606/351-005
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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