The Effect of Alpha Lipoic Acid on the Incidence and Severity of Radiotherapy-Induced Oral Mucositis in Head and Neck Cancer Patients

NCT ID: NCT05023863

Last Updated: 2021-08-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE2/PHASE3

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-09-01

Study Completion Date

2022-08-31

Brief Summary

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A prospective, randomized, controlled, single-blinded study will be conducted at Clinical Oncology department, Ain Shams University Hospitals, assessing the effect of Alpha Lipoic Acid on the incidence and severity of radiotherapy induced oral mucositis in Head and Neck cancer patients.

Detailed Description

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All patients presenting to the Clinical Oncology department, Ain Shams University Hospitals, will be assessed for eligibility as follow:

Inclusion criteria:

* Age \>18 years.
* Diagnosis of stage I, II, III or IV squamous cell carcinoma, nasopharyngeal carcinoma.
* Measurable disease on CT scan at baseline.
* Planned to receive radiotherapy with a total dose 60 grays or more divided on 30 fractions with or without cisplatin (100 mg/m2, administered intravenously every 21 days for three cycles or 40 mg/m2 administered weekly for up to 7 weeks).
* Adequate liver function (liver transaminases level \< 3 times upper normal limits and total bilirubin \< 1.5 times upper normal limits).
* Adequate kidney function (estimated glomerular filtration rate \>60 ml/min).
* Adequate bone marrow function (WBCs count \> 3000 cells/mm3, ANC count \>1500 cells/mm3 and platelets count \> 100,000 cells/mm3).

Exclusion criteria:

Patients will be excluded if they have any of the following:

* Diagnosis of Thyroid cancer.
* Presence of other primary cancers.
* Treatment with alpha lipoic acid for any other indication.
* Allergy to alpha lipoic acid.
* Pregnant or lactating women. Eligible patients will be randomized to either… Alpha Lipoic Acid Group (intervention group): 35 patients will receive radiation therapy with or without platinum-based chemotherapy in addition to alpha lipoic acid 600 mg tablets twice daily (throughout the radiotherapy period). The medication will be brought from EVA company ( an Egyptian drug company ) under the trade name of thiotacid 600 mg tablets.

Control Group: 35 Patients will receive radiation therapy with or without platinum-based chemotherapy plus placebo tablets of thiotacid throughout the radiation period

All patients will be followed up weekly to assess the incidence and severity of radiation induced oral mucositis using the radiotherapy oncology group criteria also blood samples will be drawn at baseline , after three weeks (middle of radiation period) at the end of radiation period to asses changes in CRP and TAC levels

Conditions

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Radiation-Induced Mucositis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

A prospective, randomized, controlled, single blinded study
Primary Study Purpose

PREVENTION

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors

Study Groups

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Alpha Lipoic Acid Group (intervention group)

35 patients will receive radiation therapy with or without platinum-based chemotherapy in addition to alpha lipoic acid 600 mg tablets twice daily (throughout the radiotherapy period). .

Group Type ACTIVE_COMPARATOR

Alpha Lipoic Acid 600 MG Oral Tablets

Intervention Type DRUG

Alpha Lipoic Acid (ALA) is a drug which has been used in treatment of diabetic neuropathy . It act through enhancing nitric oxide-mediated endothelium-dependent vasodilation, thus improving microcirculation in patients with diabetic polyneuropathy. It is considered a safe drug, generally with a daily dose of 200 to 2400 mg/day is considered tolerable without significant side effects. Only gastrointestinal tracts side effects like nausea, vomiting, dyspepsia and abdominal pain have been described in some clinical trials. Also FDA experts confirm its safety and efficacy in humans

radiation or concurrent chemoradiation

Intervention Type RADIATION

radiation or concurrent radiotherapy plus platinum-based chemotherapy

Control Group

35 Patients will receive radiation therapy with or without platinum-based chemotherapy in addition to placebo tablets twice daily (throughout the radiotherapy period)

Group Type PLACEBO_COMPARATOR

Placebo tablets

Intervention Type OTHER

placebo tablets of the same generic of active drug which contain all the same ingredients as active tablets except alpha lipoic acid

radiation or concurrent chemoradiation

Intervention Type RADIATION

radiation or concurrent radiotherapy plus platinum-based chemotherapy

Interventions

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Alpha Lipoic Acid 600 MG Oral Tablets

Alpha Lipoic Acid (ALA) is a drug which has been used in treatment of diabetic neuropathy . It act through enhancing nitric oxide-mediated endothelium-dependent vasodilation, thus improving microcirculation in patients with diabetic polyneuropathy. It is considered a safe drug, generally with a daily dose of 200 to 2400 mg/day is considered tolerable without significant side effects. Only gastrointestinal tracts side effects like nausea, vomiting, dyspepsia and abdominal pain have been described in some clinical trials. Also FDA experts confirm its safety and efficacy in humans

Intervention Type DRUG

Placebo tablets

placebo tablets of the same generic of active drug which contain all the same ingredients as active tablets except alpha lipoic acid

Intervention Type OTHER

radiation or concurrent chemoradiation

radiation or concurrent radiotherapy plus platinum-based chemotherapy

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

* • Age \>18 years.

* Diagnosis of stage I, II, III or IV squamous cell carcinoma, nasopharyngeal carcinoma.
* Measurable disease on CT scan at baseline.
* Planned to receive radiotherapy with a total dose 60 grays or more divided on 30 fractions with or without cisplatin (100 mg/m2, administered intravenously every 21 days for three cycles or 40 mg/m2 administered weekly for up to 7 weeks).
* Adequate liver function (liver transaminases level \< 3 times upper normal limits and total bilirubin \< 1.5 times upper normal limits).
* Adequate kidney function (estimated glomerular filtration rate \>60 ml/min).
* Adequate bone marrow function (WBCs count \> 3000 cells/mm3, ANC count \>1500 cells/mm3 and platelets count \> 100,000 cells/mm3).

Exclusion Criteria

* ● Diagnosis of Thyroid cancer.

* Presence of other primary cancers.
* Treatment with alpha lipoic acid for any other indication.
* Allergy to alpha lipoic acid.
* Pregnant or lactating women.
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

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Bishoy Anwar

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Ain Shams University

Cairo, , Egypt

Site Status

Countries

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Egypt

Central Contacts

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Bishoy Anwar Rizk-Allah, bachelor

Role: CONTACT

01228016836

References

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Other Identifiers

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PHLCLINICAL

Identifier Type: -

Identifier Source: org_study_id

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