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Assessment of efficacy of weekly paclitaxel chemotherapy in ovarian cancers

Phase 2
Conditions
Advanced Ovarian Cancer.
Malignant neoplasm of ovary
Registration Number
IRCT2017050333789N1
Lead Sponsor
Taleghani Hospital- Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
14
Inclusion Criteria

Age over 18yr; Ovarian cancer confirmed by biopsy and pathology; Advanced disease confirmed by CT scan (Stage III or IV); No previous history of chemotherapy; Good liver and lung functional status; No candidate for primary surgery due to underlying disease; Full access to patients medical documents; Patient satisfaction for study participation

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Progression-free survival (PFS). Timepoint: At the end of followup study. Method of measurement: Cancer free duration after end of tratment period.
Secondary Outcome Measures
NameTimeMethod
Anemia. Timepoint: After each 21 day treatment course. Method of measurement: CBC.;Neutropenia. Timepoint: After each 21 day treatment course. Method of measurement: CBC.;Trombocytopenia. Timepoint: After each 21 day treatment course. Method of measurement: CBC.;Neuropathy. Timepoint: After each 21 day treatment course. Method of measurement: Clinical Exam.
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