Skip to content

Comparison the results of combination platinium based neoadjuvant chemotherapy regimens using gemcitabin/ciplatin with carboplatin/paclitaxel in advanced stage ovarian cancer patients; A RCT

Comparison the results of combination platinium based neoadjuvant chemotherapy regimens using gemcitabin/ciplatin with carboplatin/paclitaxel in advanced stage ovarian cancer patients; A RCT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201203225283N3
Enrollment
206
Registered
2012-06-28
Start date
2009-11-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with advanced serous ovarian cancer, Figo stage III and IV. Malignant neoplasm of ovary

Interventions

Intervention 1: For first group, at first daycombination ofgemcitabin (1000 mg per square meter on days 1 and 8 IV during 30 minutes) and cisplatin (75 mg per square meter, IV) are administrated. This
Treatment - Drugs
For first group, at first daycombination ofgemcitabin (1000 mg per square meter on days 1 and 8 IV during 30 minutes) and cisplatin (75 mg per square meter, IV) are administrated. This protocol can be
For group 2, combination of carboplatin (carboplatin at an area under the concentration-time curve (AUC) of 5-6 mg/mL/min IV over 1 hour and paclitaxel (175 mg per square meter IV over 3 hours) on t

Sponsors

Women's Reproductive Health Research Center, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with advanced serous ovarian cancer Figo Stage III and IV; the volume of ascites, that is determined by ultrasound or CT scan, more than 500cc

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
CA-125 levels. Timepoint: before surgery. Method of measurement: Lab measurement.;The volume of residual tumor. Timepoint: During surgery. Method of measurement: Clinical judgment.;The volume of ascites. Timepoint: During surgery. Method of measurement: Clinical estimation.;Bleeding. Timepoint: During surgery. Method of measurement: Clinical estimation.;Surgery duration. Timepoint: During surgery. Method of measurement: During surgery.;Death during surgery. Timepoint: During surgery. Method of measurement: observation.

Secondary

MeasureTime frame
Wound infection, dehicsence, nausea, vomiting,diarrhea, illeus, intestinal obstruction, hospital stay. Timepoint: 24 h after surgery. Method of measurement: observation, ultrasonography, CT-scan.;Ascites collection. Timepoint: 24 hours after surgery. Method of measurement: observation, ultrasonography, CT-scan.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactManizheh Sayyah-Melli

Tabriz University of Medical Sciences

manizheh.sayyahmelli@gmail.com+98 41 1553 9161

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026