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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03151213
Other study ID # amr magdy
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date May 1, 2017
Est. completion date December 2019

Study information

Verified date August 2018
Source Tanta University
Contact Sherief Abd-Elsalam, consultant
Phone 00201095159522
Email Sheriefabdelsalam@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aimed to investigate the preemptive analgesia efficacy of of preemptive pregabalin for the postoperative pain management after radiofrequency ablation (RFA) of liver cancer.


Description:

Our data will investigate if preemptive administration of pregabalin will have a role in reducing postoperative pain after radiofrequency ablation (RFA) of liver cancer.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- HCC patients, Child A, B, scheduled for Radiofrequency ablation of HCC.

Exclusion Criteria:

- Encephalopathy, Renal impairment

Study Design


Intervention

Drug:
Pregabalin 150mg
Pregabalin 150mg before RFA of liver cancer
Other:
Placebo
Placebo before RFA of liver cancer

Locations

Country Name City State
Egypt Tanta university - faculty of medicine Cairo Elgharbia

Sponsors (1)

Lead Sponsor Collaborator
Sherief Abd-Elsalam

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary visual analogue pain scale (VAS Pain) post operatively Amplitude of pain postoperatively 2 weeks
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