|
Main
|
|
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
|
Register:
|
ChiCTR |
|
Last refreshed on:
|
18 April 2017 |
|
Main ID: |
ChiCTR-IPR-16007903 |
|
Date of registration:
|
2016-02-05 |
|
Prospective Registration:
|
Yes |
|
Primary sponsor: |
|
|
Public title:
|
Postoprative analgesia effect by oxycodone hydrochlorid in laryngectomy
|
|
Scientific title:
|
Postoprative analgesia effect by oxycodone hydrochlorid in laryngectomy |
|
Date of first enrolment:
|
2016-02-06 |
|
Target sample size:
|
oxycodone group:45;morphine group:45; |
|
Recruitment status: |
Recruiting |
|
URL:
|
http://www.chictr.org.cn/showproj.aspx?proj=13341 |
|
Study type:
|
Interventional study |
|
Study design:
|
Randomized parallel controlled trial
|
|
Phase:
|
Post-market
|
|
|
Countries of recruitment
|
|
China
| | | | | | | |
|
Contacts
|
|
Name:
|
Wenxian Li
|
|
Address:
|
83 Fenyang Road, Xuhui District, Shanghai
|
|
Telephone:
|
+86 13917426838 |
|
Email:
|
wenxianli66@gmail.com |
|
Affiliation:
|
|
|
|
Name:
|
Wenxian Li
|
|
Address:
|
83 Fenyang Road, Xuhui District, Shanghai
|
|
Telephone:
|
+86 13917426838 |
|
Email:
|
wenxianli66@gmail.com |
|
Affiliation:
|
Eye and ENT Hospital of Fudan University |
| |
|
Key inclusion & exclusion criteria
|
Inclusion criteria: Patients with full ability to communicate undergoing selective laryngectomy, ASA status I-II, aged 20-69 years old, no restriction on gender
Exclusion criteria: 1. Patients allergic to oxycodone hydrochlorid or any drugs used during this study;
2. patients on long-term therapy with narcosis analgeticsedative or non-steroid anti-inflammatory drugs;
3. patients with neuromuscular disorders;
4. patients with allergic disorders;
5. other situations unsuitable for this study
Age minimum:
20
Age maximum:
69
Gender:
Both
|
|
Health Condition(s) or Problem(s) studied
|
|
post operative pain
|
|
Intervention(s)
|
|
oxycodone group:patient-controlled intravenous analgesia with oxycodone hydrochlorid;morphine group:patient-controlled intravenous analgesia with morphine hydrochlorid;
|
|
Primary Outcome(s)
|
|
drug consumption;drug recruitment;total bolus;VAS scores;
|
|
Secondary Outcome(s)
|
|
Ramsay scores;SBP,DBP,MAP,HR,SpO2;cough scores;Nausea scores;vomiting scores;
|
|
Source(s) of Monetary Support
|
|
Personal
|
|
Results
|
|
Results available:
|
|
|
Date Posted:
|
|
|
Date Completed:
|
|
|
URL:
|
|
|
|