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RecruitingNCT07256119Updated Dec 12, 2025

Evaluation of the Effect of Alpha Lipoic Acid on Radiation Induced Dermatitis in Breast Cancer Patients

An interventional study of Alpha Lipoic Acid in Prevention, sponsored by Ain Shams University. Recruiting at 1 site in Egypt. Open to female participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2025-12-12.

Sponsored by Ain Shams University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Dec 2025, 9 months ago, but the record still lists the study as recruiting.
  • Registered 1 year 3 months after the study started (first participant enrolled Aug 2024, registered Nov 2025).
  • Started Aug 2024; still recruiting 2 years 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
Female
01

Study summary

the purpose of this study is to evaluate the Effect of Alpha Lipoic Acid on Radiation Induced Dermatitis in Breast Cancer Patients

Read the detailed description

Cancer is one of the leading causes of mortality worldwide, and cancer treatment options include chemotherapy, radiotherapy, surgery, and hormone therapy. Radiation therapy is a treatment based on the use of high-energy waves or radioactive particles to damage tumor cells to attenuate their growth. This modality has been effectively used for cancer treatment in more than 100 years.

Radiation therapy (RT) is one of the standard protocols with a high success rate for the treatment of breast cancer to reduce the risk of recurrence and death. The goal of radiation therapy is to destroy tumor cells with minimal damage to normal tissue. However, normal cells may be damaged when exposed to radiation.

Radiation-induced dermatitis (RID) occurs in 95% of patients receiving radiation therapy during their treatment. The skin cells located in close vicinity to the tumor cells receive large amounts of radiation, causing several complications such as redness, dry and wet desquamation, and tissue necrosis.

The occurrence of these complications in patients leads to discomfort, limited daily activities, and even stops radiotherapy, which negatively affects the cancer treatment. Symptoms usually appear 10-14 days following the initiation of treatment and carry on for 2 to 4 weeks during radiation therapy. Previous studies evaluated the effect of various topical and oral formulations in radiation-induced dermatitis. However, until now, there is no standard measure for the prevention of radiation-induced dermatitis in patients with breast cancer.

The mechanisms associated with radiation-induced dermatitis include inflammatory response and oxidative stress (OS). Inflammatory response and oxidative stress interact and promote each other. After radiation-induced cell damage, cells die in various forms, especially mitotic death, leading to inflammation and chronic oxidative stress. Understanding the mechanisms of chronic oxidative damage and injury of affected cells, tissues, and organs after exposure to radiation therapy may contribute to the development of treatment and management strategies of the complications associated with radiation therapy.

Inflammatory response

In the initial period of radiation therapy, there is an immediate generation of an inflammatory response. The early inflammatory response to radiation is mainly caused by pro-inflammatory cytokines (IL-1, IL-3, IL-5, IL-6, and tumor necrosis factor [TNF]-a), chemokines (eotaxin and IL-8), receptor tyrosine kinase, and adhesions molecules (intercellular adhesion molecule 1 [ICAM-1], E-selectin, and vascular cell adhesion protein). These factors can create a local inflammatory response of eosinophils and neutrophils, leading to self-perpetuating tissue damage and loss of protective barriers.

Oxidative stress (OS)

Chronic oxidative stress participates in the development of several diseases. The redox system plays a key role in the early and late effects of radiation-induced skin reactions (RISRs).

As 80% of the tissues and cells are made of water, much of the radiation damage from exposure to low linear energy transfer radiation (Photon\& electrons) is due to radiolysis of water leading to the generation of reactive oxygen species (ROS) and reactive nitrogen species (RNS), which are important mediators for some cellular processes such as immune response, cell signaling, microbial defenses, differentiation, cell adhesion, and apoptosis. The reactive oxygen species and reactive nitrogen species are the major sources of normal tissue damage after exposure to radiation therapy. The production of reactive oxygen species undergoes molecular changes, damaging DNA, lipids, and proteins and activating early-response transcription factors and signal transduction pathways. As a result, it causes damage to the skin tissue.

Inflammation plays a key role in redox activation. Direct exposure of normal cells to IR or ROS leads to nuclear and mitochondrial DNA damage, which may result in cell death through apoptosis and necrosis. Cell apoptosis can trigger the release of anti-inflammatory cytokines such as interleukin-10 (IL-10) and Transforming Growth Factor-beta (TGF-β), while necrosis may cause the release of pro-inflammatory cytokines such as interleukin-1 (IL-1), interleukin-6 (IL-6),interleukin-8 (IL-8),interleukin-13 (IL-13), interleukin-33 (IL-33), and tumor necrosis factor alpha (TNF-a) and other inflammatory mediators.

It is known that oxygen radicals and nitrogen-centered radicals regulate transcription factors, such as nuclear factor kappa-light-chain-enhancer of activated B cells (NF-KB) and activator protein 1 (AP-1). NF-KB can be activated by cellular exposure to ultraviolet or ionizing radiation, infection, or trauma. This stimulus results in the dissociation of the inhibitory portion of the molecule, followed by translocation of NF-KB to the nucleus; the result in expression of genes that are linked to the inflammatory response.

Based on literature, Alpha-lipoic acid (ALA) is a pleiotropic medication with anti-inflammatory and antioxidant properties, of which the effects are exerted through the modulation of NF-kB which modulates inflammatory cytokines, including interleukin -1β (IL-1β) and interleukin-6 (IL-6), in different cell types and tissues. Additionally, Alpha-lipoic acid has the ability to combat oxidative damage via quenching a variety of intracellular free radicals. In addition, alpha-lipoic acid is involved in the recycling of some other natural cellular reactive oxygen species scavengers such as ascorbic acid, α-tocopherol, and glutathione (GSH).

Hence, many clinical trials have been using Alpha Lipoic Acid, to see its anti-inflammatory and antioxidant effects in different indications including Alzheimer's disease patients as Studies recently showed that interleukin -1β (IL-1β) and interleukin-6 (IL-6) DNA methylation is modulated in the brain of Alzheimer's disease patients. and alpha-lipoic acid induced repression of interleukin -1β (IL-1β) and interleukin-6 (IL-6) was dependent on DNA methylation, several studies show that alpha-lipoic acid has greet effect on patients with metabolic syndrome as it diminishes pro-inflammatory markers and enhances endothelial function, elements that are indicated in the pathogenesis of atherosclerosis. Along with that, it was also found that alpha-lipoic acid supplementation improved serum adiponectin and interleukin-6 (IL-6) levels, without changing serum liver enzymes and liver steatosis in obese patients with Non-alcoholic fatty liver disease, and in Diabetic patients with neuropathy treated with alpha-lipoic acid 600 mg daily for three weeks, have reduced pain, paresthesia, and numbness.

Previous studies demonstrated the safety and tolerability of alpha-lipoic acid in doses ranging from 600-1800 mg/day.

02

Conditions studied

  • Prevention

Keywords

  • Radiation Induced Dermatitis
  • RID
  • Alpha Lipoic Acid
  • Breast Cancer
03

In context

Radiodermatitis

134 studies on the registry are indexed under Radiodermatitis; 26 are open to participants now.

This study's planned enrollment of 40 is below the median of 58 across 109 interventional studies indexed under Radiodermatitis.

Browse Radiodermatitis studies →

Lead sponsor

Ain Shams University is the lead sponsor of 1,876 studies on the registry; 423 are open to participants now.

Of its 32 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Women aged ≥18 years.
  • Histologically confirmed invasive, early-stage breast carcinoma scheduled for adjuvant radiotherapy.
  • Receiving total radiation dose of 40 Gy for 15 sessions.

Exclusion criteria

Exclusion Criteria:

  • Prior exposure to radiotherapy.
  • Inflammatory or metastatic breast carcinoma.
  • Patients with connective tissue disorders.
  • Patients with skin inflammatory diseases (e.g. ectopic dermatitis).
  • Patients with known allergy or hypersensitivity to alpha lipoic acid.
  • Concomitant use of nonsteroidal anti-inflammatory drugs, corticosteroids, or antioxidant medications.
  • Patients who will fail to sign the written consent.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    alpha lipoic acid

    patients will receive alpha lipoic acid 300 mg three times daily under the trade name of THIOTACID manufactured by EVAPHARMA for prophylaxis of the radiation-induced dermatitis (RID) from day 1 of radiation therapy till the end of the study.

    Dietary Supplement: Alpha Lipoic Acid

  • No intervention
    Control

    patients will not receive any prophylactic intervention as there is no standard of care for prophylaxis to the radiation-induced dermatitis (RID).

Interventions

  • Dietary supplementAlpha Lipoic Acid

    alpha lipoic acid 300 mg three times daily under the trade name of THIOTACID manufactured by EVAPHARMA.

06

What researchers measure

Primary outcomes

  1. Incidence of development of radiation induced dermatitis (RID)

    If the patient developed Radiation induced dermatitis or not.

    Time frame: weekly after every fifth Radiotherapy session till the end of study (3 weeks).

  2. Evaluation of the Severity of radiation-induced dermatitis (RID) developed

    severity will be scored using the Radiation Therapy Oncology Group (RTOG) criteria based on the clinical presentation.

    Time frame: weekly after every fifth Radiotherapy session till the end of study (3 weeks).

  3. Evaluation of Inflammatory biomarker level (Interleukin-6)

    Assessing Serum level of Interleukin-6 (IL6) using ELISA kits.

    Time frame: baseline, end of study Up to 3 Weeks

  4. Evaluation of Incidence of Treatment-Emergent Adverse Events

    Patients will be educated and instructed to report any adverse events.

    Time frame: weekly after every fifth Radiotherapy session till the end of study (3 weeks).

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 12, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07256119
Lead sponsor
Ain Shams University
Responsible party
Rana mohamed (Principal Investigator, Ain Shams University) — Principal investigator
First posted
Dec 1, 2025
Start date
Aug 6, 2024
Primary completion
Dec 28, 2025 (estimated)
Completion
Dec 28, 2025 (estimated)
Last update
Dec 12, 2025

Study contacts

Rana Mohamed Elsayed Kelany Abdelkader
Contact
rana.mohamed18@pharma.asu.edu.eg
00201023262639
Rana Mohamed Elsayed Kelany Abdelkader
principal investigator · Faculty of Pharmacy, Ain Shams University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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