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NCT03222700 Clinical Trial

The Recovery Profiles After Robotic or Open Thyroidectomy

Postoperative Pain Clinical Trial

Official title:
The Recovery Profiles After Robotic or Open Thyroidectomy

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03222700
Other study ID # B-1606/351-005
Secondary ID
Status Recruiting
Phase N/A
First received July 12, 2017
Last updated July 17, 2017
Start date September 1, 2016
Est. completion date August 2018

Study information
Verified date July 2017
Source Seoul National University Hospital
Contact Yeji Lee, Pf
Phone 82317877499
Email ladydaisy82@naver.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In the present study, The investigators investigated the effect of surgical methods on the recovery of patients after robotic surgery and open thyroidectomy

Recruitment information / eligibility
Status Recruiting
Enrollment 104
Est. completion date August 2018
Est. primary completion date August 2018
Accepts healthy volunteers No
Gender All
Age group 19 Years to 70 Years
Eligibility Inclusion Criteria:

1. Patients undergoing robotic thyroidectomy or open conventional thyroidectomy

2. Adults 19 to 70 years of age

3. American Society of Anesthesiologists Physical grade 1-2

Exclusion Criteria:

1. Patients who underwent surgery on the neck and in the laryngeal area before

2. Patients who do not understand or can not express pain scale

3. Patients with sore throat and cough before surgery

4. If intubation is difficult or repeated intubation is performed

5. Patients who are using opioids or analgesics as chronic agents.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• surgical procedure
In robotic thyroidectomy group, patients are received surgery using robotic system. In open thyroidectomy group, patients are received conventional open surgery.

Locations
Country Name City State
Korea, Republic of Ah-young Oh Seongnam-si Gyeonggi-do

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary postoperative sore throat none, mild, moderate, severe postoperative 1 hour
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