Status:

UNKNOWN

Possible Protective Effect of Celecoxib Against Capecitabine Induced Hand and Foot Syndrome in Patients With Colorectal Cancer

Lead Sponsor:

Tanta University

Conditions:

Hand and Foot Syndrome

Erythrodysesthesia Syndrome

Eligibility:

All Genders

18-65 years

Phase:

PHASE3

Brief Summary

Colorectal cancer (CRC) is the third most common cancer and the second leading cause of malignancy-related mortality. Capecitabine has been approved for the treatment of colorectal cancer as first-lin...

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • Age: 18-65 years old.
  • Gender: Male and female.
  • Newly diagnosed colorectal cancer patients who are scheduled to receive capecitabine-based chemotherapy.
  • Eastern Cooperative Oncology Group (ECOG) performance status \< 2
  • Patients with adequate renal function (Sr. creatinine \< 1.2 mg/dl or eGFR ≥ 90 ml/min).
  • Patients with adequate hepatic function (Sr. bilirubin \< 1.2 mg/dl).
  • Exclusion criteria:
  • Pregnant and lactating females.
  • Patients with cardiovascular disease (congestive heart failure, cardiac arrhythmia, or coronary artery disease, …. etc.).
  • History of H-Pylori infection.
  • Patients with a known hypersensitivity to any of the used drugs.
  • Patients with any contraindication to any of the used drugs.

Exclusion

    Key Trial Info

    Start Date :

    April 1 2022

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ESTIMATED

    End Date :

    April 1 2025

    Estimated Enrollment :

    44 Patients enrolled

    Trial Details

    Trial ID

    NCT05327751

    Start Date

    April 1 2022

    End Date

    April 1 2025

    Last Update

    April 14 2022

    Active Locations (1)

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    Faculty of Pharmacy-Tanta University

    Tanta, Egypt