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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02606539
Other study ID # GTN and surgery
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received August 8, 2015
Last updated March 21, 2017
Start date September 2015
Est. completion date August 2017

Study information

Verified date November 2015
Source Mansoura University
Contact maher elesawi, Msc
Phone 01016103662
Email maherelesawi@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Gestational trophoblastic neoplasm affect women and is sensitive to chemotherapy especially methotrexate and the investigators try to find a role of surgery plus methotrexate instead of multiple doses and cycles of chemotherapy.


Description:

Gestational trophoblastic neoplasm affect women and is sensitive to chemotherapy espechialy methotrexate and the investigators try to find a role of surgery plus mehotrexate instead of multiple doses and cycles of chemotherapy that affect the patient quality of life and complication related to both line of management and time of decrease of B-hcg.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date August 2017
Est. primary completion date June 2017
Accepts healthy volunteers No
Gender Female
Age group 40 Years and older
Eligibility Inclusion Criteria:

- females

- 40 years or more

- plateau or rising B- hCG titre

- without distant metastasis

- WHO score is less than 7

Exclusion Criteria:

- less than 40 years

- distant metastasis to lung and liver

- chronic medical diseases

- WHO score is more than 7

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Total abdominal hysterectomy and methotrexate
After written consent laparotomy will be done then pelvic examination for extra uterine spread, palpation of liver, omentum for any gross lesions and then hystrectomt bilateral salpigooophrectomy will be done) plus single course methotrexate(anti folate chemotheraputic agent, vial form given by intramuscular injection) 1mg/kg every other day alternating with calcium folinate 0.1 mg/kg for 4 doses each cycle then measuring B-HCG (the cycle may be repeated until normalization of B-HCG)
Drug:
Methotrexate plus folinic acid alone
methotrxate 1mg/kg every other day alternating with calcium folinate 0.1 mg/kg for 4 doses each cycle then measuring B-HCG and cycle repeated until normalization of B-HCG

Locations

Country Name City State
Egypt Mansoura University Hospital Mansoura Dakahlia
Egypt Maher Elesawi Kamel Elesawi Mit Ghamr Eldakahlia

Sponsors (1)

Lead Sponsor Collaborator
Maher elesawi kamel elesawi

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of primary chemotherapy courses till B-hCG reach less than 5 MU/ML 1-6 months
Secondary quality of life( questionairre) pain scale from zero to 11, return to ordinary activities 1-6 months
Secondary complications from management renal, hepatic impairments, anemia, 1-6 months
Secondary time interval for B-hCG reach less than 5 MU/ML the time taken for B-hCG to reach below 5 MU/ML 1-6 months
See also
  Status Clinical Trial Phase
Recruiting NCT02639650 - Study of Paclitaxel Plus Cisplatin as the First-line Chemotherapy in High Risk Gestational Trophoblastic Tumor Phase 3
Active, not recruiting NCT01823315 - Methotrexate Single-dose Treatment and Methotrexate/Actinomycin-D Single-dose Treatment in Low-Risk Gestational Trophoblastic Neoplasia Phase 3