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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04797546
Other study ID # 16-128
Secondary ID
Status Withdrawn
Phase Phase 1
First received
Last updated
Start date September 2016
Est. completion date November 2018

Study information

Verified date September 2016
Source Pontificia Universidad Catolica de Chile
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the surgical stress response in anterior cruciate ligament repair with an adductor canal block versus patient controlled endovenous analgesia.


Description:

Preoperative, 2 hours and 24 hours stress biomarkers will be evaluated in two groups of patients, continous adductor canal block and morphine patient controlled endovenous analgesia.


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Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Adductor Canal Block
Continous peripheral nerve block
Device:
Morphine Patient Controlled Analgesia
Morphine Patient Controlled Analgesia Delivery System

Locations

Country Name City State
Chile Pontificia Universidad Católica de Chile Santiago

Sponsors (1)

Lead Sponsor Collaborator
Pontificia Universidad Catolica de Chile

Country where clinical trial is conducted

Chile, 

References & Publications (11)

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Outcome

Type Measure Description Time frame Safety issue
Primary Change of Blood Cortisol from baseline to 24 hours Blood Cortisol will be evaluated preoperatively, 2 hours and 24 hours postoperatively. 24 hours
Secondary Change of C Reactive Protein from baseline to 24 hours C Reactive Protein will be evaluated preoperatively, 2 hours and 24 hours postoperatively. 24 hours
Secondary Change of Glycemia from baseline to 24 hours Glycemia will be evaluated preoperatively, 2 hours and 24 hours postoperatively. 24 hours
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