Motor Cortex Versus Insula Stimulation Using Transcranial Current Stimulation on Chronic Post-mastectomy Pain

Post-Mastectomy Chronic Pain Syndrome Clinical Trial

Official title:

Effect of Motor Cortex Versus Insula Cortical Targets Stimulation Using Concentric Electrode Transcranial Direct Current Stimulation on Chronic Post-mastectomy Pain; a Randomized Sham Controlled Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05544604
• Other study ID #: 453
• Status: Completed
• Phase: N/A
• Start date: May 1, 2020
• Est. completion date: December 14, 2022

Study information

• Verified date: December 2022
• Source: South Egypt Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is designed to evaluate the effect of two concentric electrode transcranial direct current stimulation over the primary motor cortex versus insular cortical targets in post mastectomy neuropathic pain.

Description:

eighty patients within age group 18-65 years old with post mastectomy neuropathic pain that are resistant to medical treatment in the form of tramadol hydrochloride 100 mg twice daily, pregabalin 75 mg twice daily and Amitriptyline 25 mg once daily for at least two months or associated with significant adverse effect from medication will be involved in this study. twenty patients will be randomly allocated into one of the study designed groups using serially numbered opaque closed envelopes. Each patient will be placed in the appropriate group after opening the corresponding sealed envelope. The patient will receive one of the following interventions either: - active tDCS (2 mA) targeting the primary motor cortex of the contralateral side of the pain for 20 minute duration for five sessions in five consecutive days (one session /day), - sham tDCS over the primary motor cortex in the same stimulation parameters will be used but the device will be turned off without patient knowledge after 30 seconds , - active tDCS (2mA) targeting the insula of the contralateral side of the pain for 20 minute duration for five sessions in five consecutive days (one session /day), - sham tDCS over the insula in the same stimulation parameters will be used but the device will be turned off without patient knowledge after 30 seconds.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: December 14, 2022
• Est. primary completion date: December 30, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• eighty patients within age group 18-65 years old with post mastectomy neuropathic pain that are resistant to medical treatment in the form of tramadol hydrochloride 100 mg twice daily, pregabalin 75 mg twice daily and Amitriptyline 25 mg once daily for at least two months or associated with significant adverse effect from medication will be involved in this study.

Exclusion Criteria:

• We will exclude patients with intracranial metallic devices or with pacemakers or any other device. We also exclude those with extensive myocardial ischemia and those known to have epilepsy

Related Conditions & MeSH terms

• Chronic Pain
• Post-Mastectomy Chronic Pain Syndrome

Intervention

Device:
• Transcranial direct current stimulation
tDCS will be delivered with current strength of 2 mA for 20 min . Current will be applied through two concentric electrodes target electrode; return electrode. First we will fill the electrode cage with an electroconductive gel, and then position the electrodes, with the target electrode over the FDI hotspot, and finally we fasten the electrodes with a tubular net-shaped elastic bandage in mesh tissue, making sure that it will not push the electrode forward or backward. This procedure will aim at reducing contact impedance and at creating a uniform adherence between the whole surface of the electrodes and the scalp, avoiding uneven distribution of the current (Fertonani, 2015). We will position the central electrode (anode) according to the study group over C3 or C4 , the stimulating electrode will be placed on the scalp at T7 or T8 for the insular cortex per the 10-20 (EEG) system.

Locations

Country	Name	City	State
Egypt	South Egypt Cancer Institute	Assiut

Sponsors (2)

Lead Sponsor	Collaborator
South Egypt Cancer Institute	Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	chronic postmastectomy pain relief	pain relief on the VAS after the 5th session	VAS monitoring after 5th session
Primary	chronic postmastectomy pain relief	pain relief on the VAS after 15 days	VAS monitoring after 15 days
Primary	chronic postmastectomy pain relief	pain relief on the VAS 1 month later	VAS monitoring one month later
Secondary	VDS, LANSS and depression symptoms by HAM-D	VDS, LANSS and depression symptoms by HAM-D after the 5th session	VDS, LANSS and depression symptoms by HAM-D after 5th session
Secondary	VDS, LANSS and depression symptoms by HAM-D	VDS, LANSS and depression symptoms by HAM-D after 15 days	VDS, LANSS and depression symptoms by HAM-D after 15 days
Secondary	VDS, LANSS and depression symptoms by HAM-D	VDS, LANSS and depression symptoms by HAM-D 1 month later	VDS, LANSS and depression symptoms by HAM-D after one month