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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04505280
Other study ID # 2011-KAEK-2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date December 30, 2022

Study information

Verified date February 2023
Source Dr. Lutfi Kirdar Kartal Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate the efficacy of greater occipital nerve block and cervical injections with lidocaine


Description:

After being informed about the study and potantiel risks, all patients giving informed consent will undergo randomization in 1:1 ratio to 1% lidocaine or 0.9% saline groups


Recruitment information / eligibility

Status Completed
Enrollment 29
Est. completion date December 30, 2022
Est. primary completion date October 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Classical Trigeminal Neuralgia Exclusion Criteria: - Secondary Trigeminal Neuralgia

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Lidocaine 1% Injectable Solution
Greater occipital nerve and cervical region injections once a week for 4 weeks

Locations

Country Name City State
Turkey Afyonkarahisar University of Health Sciences Afyonkarahisar Kartal/Soganlik

Sponsors (1)

Lead Sponsor Collaborator
Dr. Lutfi Kirdar Kartal Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacy on pain severity Efficacy on pain scores. Visual Analogue Scale (VAS). VAS is a ten-point scale where zero refers to no pain and ten refers to maximal pain 3 months
Primary Efficacy on pain frequency Pain frequency per day 3 months
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