Who is sponsoring NCT06836596?

NCT06836596 is sponsored by Suez University.

What drugs are being tested in NCT06836596?

Interventions in NCT06836596: Peripheral sensory electrical stimulation via Elettronica Pagani Roland series model: ET 20 S/N: 1907 (Made in Italy), Alternating electromyogram (EMG) neuromuscular electrical stimulation via MyoTrac Infiniti device (T9800, Thought Technology Ltd. Montreal, Quebec, Canada).

What condition does NCT06836596 study?

NCT06836596 studies Chronic Stroke Survivors, Chronic Stroke Survivors With Plegic Hand.

Is NCT06836596 still recruiting?

NCT06836596 is currently completed. Last updated 20 February 2025.

Last reviewed 2025-02-20 · How we verify

NCT06836596

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

Efficacy of Sensory Electrical Stimulation Versus Alternating Electromyogram (EMG) On Functional Recovery Of Hand in Chronic Stroke Survivors :Randomized Controlled Trial

Completed NA Last updated 20 February 2025

What this trial tests

NA trial testing Peripheral sensory electrical stimulation via Elettronica Pagani Roland series model: ET 20 S/N: 1907 (Made in Italy) in Chronic Stroke Survivors in 60 participants. Completed in 7 February 2025.

Timeline

1 December 2023

Primary endpoint
7 December 2024

7 February 2025

Quick facts

Lead sponsor	Suez University
Phase	NA
Status	Completed
Study type	INTERVENTIONAL
Allocation	randomized
Design	parallel
Masking	none
Primary purpose	treatment
Enrollment	60
Start date	1 December 2023
Primary completion	7 December 2024
Estimated completion	7 February 2025
Sites	1 location across Egypt

Drugs / interventions tested

Peripheral sensory electrical stimulation via Elettronica Pagani Roland series model: ET 20 S/N: 1907 (Made in Italy)
Alternating electromyogram (EMG) neuromuscular electrical stimulation via MyoTrac Infiniti device (T9800, Thought Technology Ltd. Montreal, Quebec, Canada)

Conditions studied

Chronic Stroke Survivors — all drugs for Chronic Stroke Survivors →
Chronic Stroke Survivors With Plegic Hand — all drugs for Chronic Stroke Survivors With Plegic Hand →

Sponsor

Suez University

Who can join

Adults 45 to 65, any sex, with Chronic Stroke Survivors or Chronic Stroke Survivors With Plegic Hand. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to find out which treatment works better for improving hand function in stroke patients: sensory electrical stimulation or alternating electromyogram (EMG) stimulation. Both methods use electrical stimulation to help patients regain hand movement, but they work in slightly different ways. The goal is to see if one method is more effective than the other in helping stroke survivors recover their hand abilities.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

Efficacy of Sensory Electrical Stimulation Versus Alternating Electromyography (EMG) on the Functional Recovery of the Hand in Chronic Stroke Survivors: Randomized Controlled Trial
el-Sherbini ae, Habib DA, Ashraf A, Emam M, et al · · 2025 · DOI 10.21203/rs.3.rs-7836628/v1

Verify or expand the search:

Other recruiting trials for Chronic Stroke Survivors

Currently open trials in the same condition.

NCT06765642 — The Effect of Non-invasive Brain Stimulation rTMS on Hand Muscles in Chronic Stroke Patients. · NA · recruiting
NCT06690073 — The Effect of Motor Relearning Program on Functional Mobility in Stroke Rehabilitation. · NA · recruiting
NCT06470009 — Portable Neuromodulation Stimulator (PoNS®) Therapy for Gait and Balance Deficits in Chronic Stroke Survivors: A Randomi · NA · active not recruiting
NCT06336720 — PoNS® Therapy for Gait and Balance Deficits in Chronic Stroke Survivors: A Single-Arm Study · NA · active not recruiting

Other Suez University trials

Trials by the same sponsor.

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NCT07074626 — Local Lidocaine Gel for Pain Management During · active not recruiting
NCT06966219 — Trigger Protocol on the Rate of Pregnancy After Intracytoplasmic Sperm Injection · active not recruiting
NCT06888414 — Evaluation of the Uterine Cavity in Perimenopausal Women. · active not recruiting
NCT06349876 — Cholecystectomy in Patients With Silent Common Bile Duct Stones · completed

Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT06836596 (US National Library of Medicine, public domain)
Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Suez University
Last refreshed: 20 February 2025

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06836596.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing