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Recruiting NCT05693597

Evaluation of the Effect of Nigella Sativa for the Prophylaxis to Radiation Induced Dermatitis in Breast Cancer Patients

Conditions: Radiation Dermatitis

Sex: Female
Ages: 18 Years – 75 Years
Phase: PHASE2
Enrollment: 132
Sponsor: German University in Cairo

Location: Egypt

Summary

Radiation induced dermatitis (RID) is one of the leading adverse events of radiation therapy, and if occurred could alter the course of therapy. The main pathways of RID is inflammation and oxidative stress on local and systemic bases. Nigella sativa is an herbal medicine whose anti-inflammatory and antioxidant activities have been proven in several clinical trials. Thus, the aim of the present study is to evaluate the efficacy of Nigella sativa as a prophylactic method against the development of RID.

Eligibility Criteria

Inclusion Criteria:Histologically confirmed invasive, early stage breast carcinoma scheduled for adjuvant radiotherapy.Women aged ≥18 years.Exclusion Criteria:Prior exposure to radiotherapyPatients with generalized skin disorderPatients who failed to sign the written consent

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05693597). StuddyBuddy aggregates publicly available trial information.