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Carboprost (Hemabate) for Fibroid Resection

Primary Purpose

Fibroid Uterus, Gynecologic Disease, Leiomyoma, Uterine

Status
Recruiting
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Carboprost Tromethamine
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibroid Uterus

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients scheduled to undergo myomectomy with a surgeon in the division of Minimally Invasive Gynecologic Surgery
  • Ability to understand and the willingness to sign a written informed consent

Exclusion Criteria:

  • If any oxytocic agents have been or will be administered prior to surgery
  • History of renal and/or hepatic impairment
  • Active cardiac disease, pulmonary disease, or pelvic inflammatory disease (PID)
  • Anemia (Hgb < 7g/dL), diabetes mellitus, jaundice, or epilepsy

Sites / Locations

  • Northwestern University - Northwestern Medicine, Lavin Family PavilionRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Hemabate

Arm Description

Dilute the 250mcg/mL vial with 25mL saline to create a solution of 10mcg/mL, and inject no more than 10mL of diluted solution at the base of the fibroid. The route of administration depends on the location of the fibroid.

Outcomes

Primary Outcome Measures

Does instillation of low-dose carboprost facilitate complete resection of FIGO II fibroids during hysteroscopic resection?
Pre-operative and post-operative ultrasound will be compared to measure the residual fibroid after hysteroscopic resection with carboprost installation.

Secondary Outcome Measures

To quantitatively assess the efficiency of fibroid resection after carboprost administration by analyzing the video recording from surgery
Recordings of all gynecologic surgeries on the site are recorded. The study team members will download and de-identify recordings by removing any PHI and labeling the video with the study ID assigned to the patient by the study team. The video will be used to assess the efficiency of fibroid removal facilitated by low-dose carboprost. The amount of tissue and the time resected will be measured to determine the grams per minute compared to historical controls.

Full Information

First Posted
August 5, 2022
Last Updated
August 24, 2022
Sponsor
Northwestern University
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1. Study Identification

Unique Protocol Identification Number
NCT05518812
Brief Title
Carboprost (Hemabate) for Fibroid Resection
Official Title
Carboprost Tromethamine (Hemabate) for Resection of Fibroids-a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 12, 2022 (Actual)
Primary Completion Date
July 2024 (Anticipated)
Study Completion Date
July 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief Summary
The purpose of this research study is to determine if low-dose (i.e., a fraction of what is commonly used) carboprost (Hemabate) helps facilitate fibroid removal (myomectomy).
Detailed Description
Uterine fibroids, also known as leiomyomas, are estimated to affect over 80% of women by the time menopause begins. Many women are asymptomatic and remain undiagnosed, therefore the prevalence of the disease is likely underestimated. Leiomyomas are the most common neoplasms to affect women and can cause morbidities such as heavy menstrual bleeding (HMB) and infertility. According to the American College of Obstetricians and Gynecologists, one-fourth of the women with leiomyomas befit treatment, presenting with heavy or prolonged menstrual bleeding, abdominal protrusion, bowel or bladder dysfunction, infertility, recurrent pregnancy loss, painful menses, or pelvic pain. Risk factors associated with developing leiomyomas include: early menarche, use of oral hormonal contraceptives before the age of 16 years, African descent, and an increased body mass index (BMI) (StatPearls Leiomyoma). Factors that may lower the incidence of leiomyomas include: increased parity, use of depot medroxyprogesterone acetate (DMPA) or oral hormonal contraceptives for any duration. Leiomyomas are benign tumors which arise from monoclonal smooth muscle cells of the uterus (StatPearls Leiomyoma); cells mostly composed of extracellular matrix and encapsulated in a pseudocapsule of areolar tissue. These tumor cells characteristically express higher levels of estrogen and progesterone receptors than normal myometrial cells, and ovarian steroids such as estradiol and progesterone enhance leiomyoma growth. Studies have shown that the size of leiomyomas decrease after menopause when ovarian steroid hormones decline. Leiomyoma cells typically exhibit a low mitotic index. Uterine leiomyomas can impact fertility in multiple ways, for instance, leiomyomas can impede sperm migration, interrupt ovum transport or embryo implantation, and can cause early pregnancy loss. Current treatment options for management of leiomyomas including medical therapies and surgical intervention. Surgically resecting fibroids is one of the most common procedures performed for women of reproductive age. The goal of surgery is to mitigate symptoms and lower the risk of recurrence. Fibroids identified as FIGO 0 or 1 are typically resected completely at hysteroscopy. Unfortunately, fibroids categorized as FIGO 2 when approached hysteroscopically are almost never completely removed given that there can remain residual leiomyoma within the myometrium that is inaccessible. This commonly requires follow up procedures in the coming 6 months as the myometrial portion migrates into the cavity allowing it to be accessible hysteroscopically. Similarly at laparoscopy/laparotomy, FIGO 6 or 7 fibroids are easily resected completely without significant myometrial disruption. In contrast, FIGO 3-5 fibroids require a much more invasive approach into the myometrium, potentially increasing the risk of uterine rupture during pregnancy, a potentially life-threatening event. Techniques have been developed to promote intraoperative fibroid migration towards the access point (laparoscopy/laparotomy/hysteroscopy) with some success. This is a pilot study to determine whether intramural carboprost at low concentrations can facilitate fibroid migration and minimize the risk of carboprost-related side effects. Using carboprost intraoperatively is relatively simple, does not require additional instrumentation, and potentially results in a more complete resection, reducing operative times and re-operation. With the use of carboprost, the myoma is expelled due to the myometrial contraction, and the leiomyoma is shaved down to the myometrium surface, nullifying the need to deeply invade the myometrium.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibroid Uterus, Gynecologic Disease, Leiomyoma, Uterine

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hemabate
Arm Type
Experimental
Arm Description
Dilute the 250mcg/mL vial with 25mL saline to create a solution of 10mcg/mL, and inject no more than 10mL of diluted solution at the base of the fibroid. The route of administration depends on the location of the fibroid.
Intervention Type
Drug
Intervention Name(s)
Carboprost Tromethamine
Other Intervention Name(s)
Hemabate
Intervention Description
During myomectomy, low-dose carboprost will be injected at the base of the fibroid and repeated as necessary. The efficacy of low-dose carboprost is being assessed, and the total dose administered will not exceed single vial for other indications.
Primary Outcome Measure Information:
Title
Does instillation of low-dose carboprost facilitate complete resection of FIGO II fibroids during hysteroscopic resection?
Description
Pre-operative and post-operative ultrasound will be compared to measure the residual fibroid after hysteroscopic resection with carboprost installation.
Time Frame
Pre-operatively to 1 month post-operatively
Secondary Outcome Measure Information:
Title
To quantitatively assess the efficiency of fibroid resection after carboprost administration by analyzing the video recording from surgery
Description
Recordings of all gynecologic surgeries on the site are recorded. The study team members will download and de-identify recordings by removing any PHI and labeling the video with the study ID assigned to the patient by the study team. The video will be used to assess the efficiency of fibroid removal facilitated by low-dose carboprost. The amount of tissue and the time resected will be measured to determine the grams per minute compared to historical controls.
Time Frame
Through study completion, up to 2 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients scheduled to undergo myomectomy with a surgeon in the division of Minimally Invasive Gynecologic Surgery Ability to understand and the willingness to sign a written informed consent Exclusion Criteria: If any oxytocic agents have been or will be administered prior to surgery History of renal and/or hepatic impairment Active cardiac disease, pulmonary disease, or pelvic inflammatory disease (PID) Anemia (Hgb < 7g/dL), diabetes mellitus, jaundice, or epilepsy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Magdy P Milad, MD, MS
Phone
312-472-4673
Email
mmilad@nm.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Magdy p Milad, MD, MS
Organizational Affiliation
Northwestern University, Northwestern Memorial Hopsital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University - Northwestern Medicine, Lavin Family Pavilion
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Magdy P Milad, MD, MS
Phone
312-472-4673
Email
mmilad@nm.org
First Name & Middle Initial & Last Name & Degree
Adaeze A Emeka, MB, BCh, BAO
Phone
312-503-3492
Email
adaeze.emeka@nm.org

12. IPD Sharing Statement

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Carboprost (Hemabate) for Fibroid Resection

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