Letrozole as a Prophylaxis From GTN for Complete Mole Patients
Primary Purpose
Gestational Trophoblastic Disease
Status
Active
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Suction evacuation
Letrozole tablets
Sponsored by
About this trial
This is an interventional prevention trial for Gestational Trophoblastic Disease focused on measuring Aromatase Inhibitor; Letrozole; GTN; Complete Mole
Eligibility Criteria
Inclusion Criteria:
- Women were diagnosed to have CHM by ultrasound and confirmed by histopathological examination
Exclusion Criteria:
- Metastatic disease associated with HM at presentation, in which situation chemotherapy, rather than prophylactic treatment, as prescribed,
- Late diagnosis of CHM made only by histological examination of curetted material
- Uterine evacuation at another hospital and patient seen at the optimum patient care only for follow up
Sites / Locations
- Mohamed ALI Alabiad
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Control group I
Prophylactic letrozole group II
Arm Description
Patients with complete mole treated by evacuation of using suction curettage followed by conservative follow up
Patients with complete mole treated by evacuation of using suction curettage followed by 5mg daily letrozole for 10 days followed by conservative follow up
Outcomes
Primary Outcome Measures
(β-hCG) level
A quantitative human chorionic gonadotropin
(β-hCG) level
A quantitative human chorionic gonadotropin
(β-hCG) level
A quantitative human chorionic gonadotropin
(β-hCG) level
A quantitative human chorionic gonadotropin
(β-hCG) level
A quantitative human chorionic gonadotropin
(β-hCG) level
A quantitative human chorionic gonadotropin
(β-hCG) level
A quantitative human chorionic gonadotropin
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05203562
Brief Title
Letrozole as a Prophylaxis From GTN for Complete Mole Patients
Official Title
The Prophylactic Role of Aromatase Inhibitor Letrozole in Decreasing the Incidence of Gestational Trophoblastic Neoplasia in Patients With Complete Hydatidiform Mole
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 1, 2020 (Actual)
Primary Completion Date
December 1, 2022 (Anticipated)
Study Completion Date
June 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zagazig University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Prophylactic use of aromatase inhibitor is effective in decreasing the incidence of Gestational Trophoblastic Neoplasia (GTN) in patients with complete hydatidiform mole (CHM)
Detailed Description
Management of hydatidiform mole is usually evacuation followed by β-hcg surveillance to early detect cases of GTN . The risk of developing GTN is reported to be 16% to 20% in women with CHM . GTN is a potentially life-threatening malignancy but has an excellent cure rate. Trials were conducted to assess the role of prophylactic chemotherapy to prevent the development of GTN. In addition to their side effects, a meta-analysis concluded that there is insufficient evidence to support the use of prophylactic chemotherapy in clinical practice. Third-generation aromatase inhibitors such as letrozole have been shown to successfully block estrogen production in women of reproductive age. Their safety, high tolerability, low cost, and associated minimal adverse effects have all been established over several decades of clinical use and recently used successfully alone in the medical treatment of ectopic pregnancy making marked degenerative effects on the placenta.
The study hypothesizes that by inhibiting the estrogen synthetase (the aromatase enzyme) progesterone would not exert its physiological role in maintaining early pregnancy including complete hydatidiform mole. Thus, using a prophylactic aromatase inhibitor after CHM may have a role in the prevention of GTN and more effective clearance of β-hcg.
Rational GTN is a potentially life-threatening malignancy. The risk of progression of CHM to GTN is 20%. Prophylactic use of aromatase inhibitor may decrease the incidence of GTN.
Research question:
Is prophylactic use of aromatase inhibitor effective in decreasing the incidence of GTN in patients with CHM
Hypothesis Prophylactic use of aromatase inhibitor is effective in decreasing the incidence of GTN in patients with CHM
Aim of this work The study aims at figuring out whether prophylactic use of aromatase inhibitor is effective in decreasing the incidence of GTN in patients with CHM.
OBJECTIVES
To assess the incidence of GTN after the evacuation of CHM without prophylactic use of aromatase inhibitor.
To assess the incidence of GTN after the evacuation of CHM without prophylactic use of aromatase inhibitor.
To assess the side effects of aromatase inhibitor when used as a prophylaxis against GTN development in CHM cases.
PATIENTS AND METHODS
Technical design:
Setting: Department of Obstetrics and Gynecology
Sample size: 200 patients diagnosed to have CHM by ultrasound and confirmed by histopathological examination.
Operational design:
Type of the study: a randomized controlled trial.
Steps of performance and techniques that will be used
women included in the study will be subjected to the following
Preoperative
Complete history taking.
General and abdominal examination.
Routine preoperative laboratory investigations.
Ultrasound to diagnose complete hydatidiform mole.
Measurement of β-hcg level. Intraoperative
Evacuation of CHM using Suction curettage.
Tissues obtained during an evacuation will be sent for histological assessment. Post-operative
Women will be randomized classified into two groups
Control group I: Conservative follow up
Prophylactic letrozole group II 5-mg Letrozole will be administered as two 2.5-mg tablets every day for 10 days.
All Patients will receive instruction to return for β-hcg follow up which will be done weekly till complete resolution then monthly for 6 months.
Participants will be advised to receive contraception during the follow-up period.
The patients who will develop GTN in either group will be picked up and the incidence of GTN will be calculated in each group.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Trophoblastic Disease
Keywords
Aromatase Inhibitor; Letrozole; GTN; Complete Mole
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
200 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control group I
Arm Type
Active Comparator
Arm Description
Patients with complete mole treated by evacuation of using suction curettage followed by conservative follow up
Arm Title
Prophylactic letrozole group II
Arm Type
Experimental
Arm Description
Patients with complete mole treated by evacuation of using suction curettage followed by 5mg daily letrozole for 10 days followed by conservative follow up
Intervention Type
Procedure
Intervention Name(s)
Suction evacuation
Other Intervention Name(s)
Evacuation of CHM using Suction curettage
Intervention Description
both groups underwent complete mole evacuation using suction curettage.
Intervention Type
Drug
Intervention Name(s)
Letrozole tablets
Other Intervention Name(s)
5mg daily (2 tablets 2.5 gm)
Intervention Description
Group II Patients received 5mg(2tablets 2.5gm) daily letrozole for 10 days after complete mole evacuation
Primary Outcome Measure Information:
Title
(β-hCG) level
Description
A quantitative human chorionic gonadotropin
Time Frame
at the first day of evacuation
Title
(β-hCG) level
Description
A quantitative human chorionic gonadotropin
Time Frame
one month after evacuation
Title
(β-hCG) level
Description
A quantitative human chorionic gonadotropin
Time Frame
two months after evacuation
Title
(β-hCG) level
Description
A quantitative human chorionic gonadotropin
Time Frame
three months after evacuation
Title
(β-hCG) level
Description
A quantitative human chorionic gonadotropin
Time Frame
four months after evacuation
Title
(β-hCG) level
Description
A quantitative human chorionic gonadotropin
Time Frame
Five months after evacuation
Title
(β-hCG) level
Description
A quantitative human chorionic gonadotropin
Time Frame
Six months after evacuation
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Patients with complete hydatidiform mole
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women were diagnosed to have CHM by ultrasound and confirmed by histopathological examination
Exclusion Criteria:
Metastatic disease associated with HM at presentation, in which situation chemotherapy, rather than prophylactic treatment, as prescribed,
Late diagnosis of CHM made only by histological examination of curetted material
Uterine evacuation at another hospital and patient seen at the optimum patient care only for follow up
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohamed A Alabiad, MD
Organizational Affiliation
Zagazig University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mohamed ALI Alabiad
City
Zagazig
State/Province
Sharkia
ZIP/Postal Code
14150
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
3 months after final complete
IPD Sharing Time Frame
3 months after final complete
IPD Sharing Access Criteria
Contac dr Mohamed at drno99@yahoo.com
IPD Sharing URL
http://www.staffdata.zu.edu.eg/ar/ShowData/23528
Learn more about this trial
Letrozole as a Prophylaxis From GTN for Complete Mole Patients
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