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Letrozole add-on in the Treatment of Cesarean Scar Pregnancy

Primary Purpose

Cesarean Scar Pregnancy

Status
Active
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
MTX monotherapy
MTX + letrozole add-on
Sponsored by
Jagiellonian University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cesarean Scar Pregnancy focused on measuring cesarean scar pregnancy, operative hysteroscopy

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: CSP confirmed on pelvic ultrasound consent of the Bioethics Committee for termination of CSP increasing B-hCG concentrations Exclusion Criteria: heterotopic pregnancy decreasing B-hCG concentrations

Sites / Locations

  • Jagiellonian University Medical College, Department of Gynecology and Obstetrics, Clinic of Gynecological Endocrinology

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

MTX in monotherapy

MTX + letrozole add-on

Arm Description

Combined treatment with MTX followed by hysteroscopic evacuation of POC

Combined treatment with MTX + letrozole add-on followed by hysteroscopic evacuation of POC

Outcomes

Primary Outcome Measures

Blood loss during the procedure expressed as a decrease in hemoglobin concentration
Decrease in hemoglobin concentration in g/dl on day 1 after the procedure compared to the pre-procedure concentration
Blood loss volume during the procedure expressed in volume units
The volume of blood lost during the procedure in ml
Conversion rate from hysteroscopy to laparoscopy or laparotomy due to due to hemorrhage
Percentage (%) of conversion from hysteroscopy to laparoscopy or laparotomy due to hemorrhage

Secondary Outcome Measures

The effect of treatment on bone marrow function (red blood cells)
Change in red blood count (T/l) in the course of treatment (day 0,4,7)
The effect of treatment on bone marrow function (white blood cells)
Change in white blood count (G/l) in the course of treatment (day 0,4,7)
The effect of treatment on bone marrow function (platelets)
Change in platelet count (G/l) in the course of treatment (day 0,4,7)
The effect of treatment on liver function (serum total bilirubin)
Changes in the concentrations of serum total bilirubin (mg/dl) in the course of treatment (day 0,4,7)
The effect of treatment on liver function (alanine transaminase)
Changes in the concentrations of alanine transaminase (IU/l) in the course of treatment (day 0,4,7)
The effect of treatment on liver function (aspartate transaminase)
Changes in the concentrations of aspartate transaminase (IU/l) in the course of treatment (day 0,4,7)
The effect of treatment on liver function (gamma-glutamyltransferase)
Changes in the concentrations of gamma-glutamyltransferase (IU/l) in the course of treatment (day 0,4,7)
The effect of treatment on kidneys function (urea)
Changes in the concentrations of serum urea (mmol/l) in the course of treatment (day 0,4,7)
The effect of treatment on kidneys function (creatinine)
Changes in the concentrations of serum and creatinine (mg/dl) in the course of treatment (day 0,4,7)

Full Information

First Posted
April 15, 2023
Last Updated
April 29, 2023
Sponsor
Jagiellonian University
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1. Study Identification

Unique Protocol Identification Number
NCT05839574
Brief Title
Letrozole add-on in the Treatment of Cesarean Scar Pregnancy
Official Title
Evaluation of the Therapeutic Effect of Adding Letrozole to the Protocol of Combined Treatment of Cesarean Scar Pregnancy
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
December 30, 2022 (Actual)
Study Completion Date
June 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Jagiellonian 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
It is hypothesized that the inhibition of estradiol production by letrozole may interfere with physiological effects of progesterone necessary to maintain the pregnancy. There is no reference treatment of cesarean scar pregnancy (CSP) as the limited number of cases precludes the extrapolation of results. In our center we successfully use two-step treatment with methotrexate (MTX) followed by hysteroscopic removal of products of conception (POC). The time in between is needed to achieve a decrease in the trophoblast's vital potential (B-hCG fall) and its vascularization. Additional administration of letrozole could further reduce the vital potential of the pregnancy, eliminating the need for another dose of MTX, resulting in faster healing and lower rate of complications.
Detailed Description
A prospective cohort study is conducted among women with cesarean scar pregnancy (CSP). Women with increasing B-human chorionic gonadotropin (B-hCG) concentrations are included. Two study arms were planned: women treated with a single dose of 100 mg MTX intravenously and 50 mg MTX in intra-amniotic injection (day 0), along with 30 mg potassium chloride in case of positive fetal heartbeat (FH) women treated with a single dose of 100 mg MTX intravenously and 50 mg MTX in intra-amniotic injection (day 0), along with 30 mg potassium chloride in case of positive fetal heartbeat (FH) with additional use of letrozole 5 mg orally (from day 0) for 10 days. Blood parameters (B-hCG, hemoglobin, total blood count, creatinine, urea, alanine/aspartate transaminase, gamma-glutamyltransferase, bilirubin) were tested on days 0,4,7, followed by B-hCG concentration measurement every 7 days until surgery. After obtaining satisfactory decrease in B-hCG and POC vascularization, women underwent hysteroscopic evacuation of POC. Blood loss parameters, frequency of conversion from hysteroscopy to laparoscopy and laparotomy were measured. The women were given the option to choose the treatment used in the study. All enrolled women gave informed written consent to participate in the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cesarean Scar Pregnancy
Keywords
cesarean scar pregnancy, operative hysteroscopy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MTX in monotherapy
Arm Type
Active Comparator
Arm Description
Combined treatment with MTX followed by hysteroscopic evacuation of POC
Arm Title
MTX + letrozole add-on
Arm Type
Active Comparator
Arm Description
Combined treatment with MTX + letrozole add-on followed by hysteroscopic evacuation of POC
Intervention Type
Drug
Intervention Name(s)
MTX monotherapy
Intervention Description
MTX in a single dose of 100 mg intravenously and 50 mg in intra-amniotic injection (day 0), along with 30 mg potassium chloride in case of positive fetal heartbeat (FH), and subsequent hysteroscopic evacuation of products of conception (POC)
Intervention Type
Drug
Intervention Name(s)
MTX + letrozole add-on
Intervention Description
MTX in a single dose of 100 mg intravenously and 50 mg in intra-amniotic injection (day 0), along with 30 mg potassium chloride in case of positive fetal heartbeat (FH) + Letrozole in a daily dose of 5 mg (2 x 2.5 mg) orally for 10 days from day 0, and subsequent hysteroscopic evacuation of products of conception (POC)
Primary Outcome Measure Information:
Title
Blood loss during the procedure expressed as a decrease in hemoglobin concentration
Description
Decrease in hemoglobin concentration in g/dl on day 1 after the procedure compared to the pre-procedure concentration
Time Frame
up to 6 months
Title
Blood loss volume during the procedure expressed in volume units
Description
The volume of blood lost during the procedure in ml
Time Frame
up to 6 months
Title
Conversion rate from hysteroscopy to laparoscopy or laparotomy due to due to hemorrhage
Description
Percentage (%) of conversion from hysteroscopy to laparoscopy or laparotomy due to hemorrhage
Time Frame
up to 6 months
Secondary Outcome Measure Information:
Title
The effect of treatment on bone marrow function (red blood cells)
Description
Change in red blood count (T/l) in the course of treatment (day 0,4,7)
Time Frame
up to 6 months
Title
The effect of treatment on bone marrow function (white blood cells)
Description
Change in white blood count (G/l) in the course of treatment (day 0,4,7)
Time Frame
up to 6 months
Title
The effect of treatment on bone marrow function (platelets)
Description
Change in platelet count (G/l) in the course of treatment (day 0,4,7)
Time Frame
up to 6 months
Title
The effect of treatment on liver function (serum total bilirubin)
Description
Changes in the concentrations of serum total bilirubin (mg/dl) in the course of treatment (day 0,4,7)
Time Frame
up to 6 months
Title
The effect of treatment on liver function (alanine transaminase)
Description
Changes in the concentrations of alanine transaminase (IU/l) in the course of treatment (day 0,4,7)
Time Frame
up to 6 months
Title
The effect of treatment on liver function (aspartate transaminase)
Description
Changes in the concentrations of aspartate transaminase (IU/l) in the course of treatment (day 0,4,7)
Time Frame
up to 6 months
Title
The effect of treatment on liver function (gamma-glutamyltransferase)
Description
Changes in the concentrations of gamma-glutamyltransferase (IU/l) in the course of treatment (day 0,4,7)
Time Frame
up to 6 months
Title
The effect of treatment on kidneys function (urea)
Description
Changes in the concentrations of serum urea (mmol/l) in the course of treatment (day 0,4,7)
Time Frame
up to 6 months
Title
The effect of treatment on kidneys function (creatinine)
Description
Changes in the concentrations of serum and creatinine (mg/dl) in the course of treatment (day 0,4,7)
Time Frame
up to 6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: CSP confirmed on pelvic ultrasound consent of the Bioethics Committee for termination of CSP increasing B-hCG concentrations Exclusion Criteria: heterotopic pregnancy decreasing B-hCG concentrations
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Iwona M. Gawron, M.D., Ph.D.
Organizational Affiliation
Jagiellonian University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Robert Jach, Prof., Ph.D.
Organizational Affiliation
Jagiellonian University
Official's Role
Study Chair
Facility Information:
Facility Name
Jagiellonian University Medical College, Department of Gynecology and Obstetrics, Clinic of Gynecological Endocrinology
City
Krakow
ZIP/Postal Code
31-501
Country
Poland

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Letrozole add-on in the Treatment of Cesarean Scar Pregnancy

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