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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03601780
Other study ID # SM62018
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received
Last updated
Start date August 2018
Est. completion date December 2018

Study information

Verified date July 2018
Source Assiut University
Contact Seham M Moeen, MD
Phone 2413201
Email seham.moeen@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Multimodal analgesia is a rational approach to treat various components of postoperative pain.


Description:

Local anesthetic wound infiltration is widely recognized as a useful adjunct during multimodal postoperative pain management whether given before operation or perioperatively.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender All
Age group 30 Years to 65 Years
Eligibility Inclusion Criteria:

- ASA I or II, aged between 30 and 65 yr, and undergoing open renal surgery

Exclusion Criteria:

- history of adverse reactions to local anaesthetics, chronic hepatic disease, chronic renal disease chronic pain, chronic preoperative opioid consumption, psychiatric disorders which would prevent postoperative assessments,

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
local wound infiltration plus usual care
local wound infiltration plus usual care
usual care only
usual care only

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative pain Visual analogue scale ranging from 0-10 cm where 0 cm
= no pain and 10 cm = the worst imaginable pain.
The first 48 hours after surgery
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