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Dose-dense Capecitabine Schedule [7days on _7 Days Off] in Colorectal Cancer in Comparison With Standered Regimen

S

Sohag University

Status and phase

Active, not recruiting
Phase 2

Conditions

Colorectal Cancer

Treatments

Drug: Arm A:Dose_dense Capecitabine in Colorectal cancer
Drug: Arm B : standard dose Capecitabine

Study type

Interventional

Funder types

Other

Identifiers

NCT07215936
Soh_med_25_9___4MD

Details and patient eligibility

About

Dose_dense Capecitabine Schedule in colorectal cancers

Full description

Dose_dense Capecitabine schedule[7 days on_7days off] in colorectal cancer in comparison with standerd regimen

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients who diagnosed colorectal cancer Performance status ranging from 0 to 2 Both sexs

Exclusion criteria

  • pateints with other malignancy Pateints who have other comorbid diseas

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

Arm A :will receive capecitabine dose dense 1750 mg /m2 7days on treatment and 7 days off
Active Comparator group
Treatment:
Drug: Arm A:Dose_dense Capecitabine in Colorectal cancer
Arm B will receive capecitabine standard dose 1000mg/m2 2weeks on and 1 week off
Active Comparator group
Treatment:
Drug: Arm B : standard dose Capecitabine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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