Mononeuritis Multiplex Clinical Trials

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Effect of Oral Alpha-Lipoic Acid, Vitamin E, and Vitamin B Combination on Symptoms and Function in Carpal Tunnel Syndrome Following Carpal Tunnel Surgery

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Carpal Tunnel Syndrome (CTS) is a common condition that causes numbness, tingling, pain, and weakness in the hand due to compression of the median nerve at the wrist. It can affect daily activities, work performance, and quality of life. While surgery is effective in severe cases, many patients with mild to moderate CTS are initially treated with non-surgical options such as splinting and medications. However, the effectiveness of oral supplements for CTS remains uncertain. This clinical study aims to evaluate whether an oral combination of alpha-lipoic acid, Vitamin E, and Vitamin B complex can safely reduce symptoms and improve hand function in patients with Carpal Tunnel Syndrome. These supplements are believed to have antioxidant, anti-inflammatory, and nerve-protective properties, which may help reduce nerve irritation and improve nerve recovery. Participants in this study will be randomly assigned to receive either the oral supplement combination or a comparator treatment. The study is single-blinded, meaning participants will not know which treatment they are receiving. Symptoms such as pain, numbness, and hand function will be assessed over a defined follow-up period using clinical evaluation and standardized questionnaires. The main hypothesis of this study is that patients receiving the oral combination of alpha-lipoic acid, Vitamin E, and Vitamin B will experience greater improvement in symptoms and functional outcomes compared to those who do not receive the combination, without significant side effects. The results of this study may help determine whether this oral supplement combination can be used as an effective and safe conservative treatment option for patients with Carpal Tunnel Syndrome, potentially reducing the need for invasive procedures.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age more than 18 years old

• Subjects with symptoms and physical examination of CTS

• Patients with CTS going for CT release

Locations
Other Locations
Malaysia
Hospital Pakar Universiti Sains Malaysia
RECRUITING
Kubang Kerian
Contact Information
Primary
Nurhakim Bin Ibrahim, MBBCH
nurhakimibrahim@gmail.com
+60123170898
Backup
ASSOCIATE PROFESSOR ABDUL NAWFAR BIN SADAGATULLAH
nawfar@usm.my
+6097676378
Time Frame
Start Date: 2025-12-08
Estimated Completion Date: 2027-01-31
Participants
Target number of participants: 84
Treatments
Experimental: Oral Antioxidant Supplement Group
Active_comparator: Control Group
Sponsors
Collaborators: BREGO Life Sciences Sdn Bhd
Leads: Hospital Universiti Sains Malaysia

This content was sourced from clinicaltrials.gov