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NCT02704715 Clinical Trial

Postoperative Pain in Orbital Disease and Ocular Tumor

Postoperative Pain Clinical Trial

Official title:
Postoperative Pain of General Anesthesia in Orbital Disease and Ocular Tumor

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02704715
Other study ID # 2016MEKY006
Secondary ID
Status Recruiting
Phase N/A
First received February 25, 2016
Last updated March 9, 2016
Start date February 2016
Est. completion date December 2018

Study information
Verified date March 2016
Source Sun Yat-sen University
Contact Huijing Ye, Master
Phone +00862087331539
Email yehuijing@qq.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the postoperative pain after general anesthesia of orbital diseases and ocular tumor patients.

Description:

The purpose of this study is to evaluate patients diagnosed of orbital diseases or ocular tumor over 16 years old of the postoperative pain after general anesthesia , and to analyze the related factors of pain after operation.

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date December 2018
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 16 Years and older
Eligibility Inclusion Criteria:

- over 16 years old

- diagnosed as orbital disease or ocular tumor

- surgery under general anesthesia

Exclusion Criteria:

- any uncontrolled clinical problems

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• general anesthesia,orbital operation
to evaluate the pain under general anesthesia

Locations
Country Name City State
China Sun Yat-sen University Guangzhou Guangdong

Sponsors (1)
Lead Sponsor Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain numerical rating scale, NRS will be used to measure the pain 24 hours after surgery
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