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Combined Vaginal Misoprostol and Perivascular Vasopressin

Primary Purpose

Leiomyoma, Laparoscopy, Uterine Myomectomy

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Standard
Standard-vaginal misoprostol
Sponsored by
Maimonides Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Leiomyoma focused on measuring Robot-assisted, Laparoscopic, vasopressin, misoprostol, blood loss

Eligibility Criteria

18 Years - 55 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Reproductive aged women between in ages of 18 to 55 undergoing robotic assisted laparoscopic myomectomy.

Exclusion Criteria:

  1. History of adverse reaction or allergy to Vasopressin.
  2. History of adverse reaction or allergy to Misoprostol.
  3. Medical contraindication to use of Vasopressin or Misoprostol
  4. Suspicion of possible reproductive cancer with contraindication of morcellation of uterine tissue.
  5. Significant medical condition or laboratory result that in the opinion of the Investigator indicate an increased vulnerability to study subject which exposes the subject to an unreasonable risk as a result of participating.
  6. Any clinically significant even or condition uncovered during the surgery, such as excessive bleeding or decompensation, that might render the subject medically unstable to continue the study or complicate the subject's intraoperative or postoperative course.
  7. Pregnant women

Sites / Locations

  • Maimonides Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard

Standard-Vaginal Misoprostol

Arm Description

Use of laparoscopic injection of diluted vasopressin (20units in 100mL 0.9NS) prior to incision throughout the myomectomy.

Use of laparoscopic injection of diluted vasopressin (20units in 100mL 0.9NS) prior to incision throughout the myomectomy. 400mcg of misoprostol placed in the vagina at HUMI/foley placement .

Outcomes

Primary Outcome Measures

Operative Blood Loss
The amount of blood loss during robotic assisted laparoscopic myomectomy

Secondary Outcome Measures

Total Operative Time
Total time of the robotic assisted laparoscopic myomectomy
Side Effects
Side Effect profile for Misoprostol Use

Full Information

First Posted
May 7, 2018
Last Updated
December 10, 2019
Sponsor
Maimonides Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03815344
Brief Title
Combined Vaginal Misoprostol and Perivascular Vasopressin
Official Title
A Randomized Control Trial of Combined Vaginal Misoprostol and Perivascular Vasopressin During Robotic Myomectomy
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Unknown status
Study Start Date
April 26, 2017 (Actual)
Primary Completion Date
December 31, 2019 (Anticipated)
Study Completion Date
December 31, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Maimonides Medical Center

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.
No

5. Study Description

Brief Summary
Injection of Vasopressin into the uterine tissue surrounding fibroids constricts blood vessels, and has been found to be beneficial by decreasing blood flow to fibroids, and thereby resulting in less bleeding with removal. Additionally, Misoprostol has been looked at as an additional method to decrease operative blood loss given its ability to increase uterine muscle tone, which therefore constricts the amount of blood flow to the uterus.
Detailed Description
Uterine fibroids are common benign tumors affecting women, and produce symptoms severe enough to warrant treatment in 20-50% of reproductive age women, including abnormal uterine bleeding, pelvic pain, and infertility. While hysterectomy with removal of the uterus is standard of care for symptomatic uterine fibroids, women desiring future child bearing require removal of the fibroids alone via uterine myomectomy, with re-construction of the uterus after removal. A well established risk to such a procedure is the operative blood loss, which can be quite significant due to the increased blood supply fibroids accumulate. Several interventions have been looked at as potential methods to help decrease operative blood loss. Injection of Vasopressin into the uterine tissue surrounding fibroids constricts blood vessels, and has been found to be beneficial by decreasing blood flow to fibroids, and thereby resulting in less bleeding with removal. A known potential side effect of vasopressin is cardiovascular compromise, which can be catastrophic if vasopressin is inadvertently injected into the large vessels of the uterus. This limits the amount that can be safely used in surgery. Additionally, Misoprostol has been looked at as an additional method to decrease operative blood loss given its ability to increase uterine muscle tone, which therefore constricts the amount of blood flow to the uterus. While Vasopressin is more commonly used during surgery, the associated potential risks limit the amount that can be safely administered. However, the addition Misoprostol, with a relatively safe side effect profile, can further improve control of the blood supply and decrease operative blood loss. Misoprostol can be administered orally, sublingually, or as vaginal or rectal suppositories. While the systemic absorption of vaginal Misoprostol is slower in onset than the oral or sublingual routes, the effect is maintained for a longer period of time, and is more conducive to use during laparoscopic or robotic assisted myomectomies given the prolonged operative time associated with minimally invasive techniques when compared to traditional open approaches. This study aims to determine whether using vaginal Misoprostol in combination with Vasopressin is more effective at decreasing operative blood loss during robotic assisted laparoscopic myomectomy than Vasopressin alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leiomyoma, Laparoscopy, Uterine Myomectomy
Keywords
Robot-assisted, Laparoscopic, vasopressin, misoprostol, blood loss

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
36 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard
Arm Type
Active Comparator
Arm Description
Use of laparoscopic injection of diluted vasopressin (20units in 100mL 0.9NS) prior to incision throughout the myomectomy.
Arm Title
Standard-Vaginal Misoprostol
Arm Type
Experimental
Arm Description
Use of laparoscopic injection of diluted vasopressin (20units in 100mL 0.9NS) prior to incision throughout the myomectomy. 400mcg of misoprostol placed in the vagina at HUMI/foley placement .
Intervention Type
Drug
Intervention Name(s)
Standard
Other Intervention Name(s)
Perivascular vasopresssin
Intervention Description
20 units diluted in 100mL of Normal Saline injected laparoscopic needle
Intervention Type
Drug
Intervention Name(s)
Standard-vaginal misoprostol
Other Intervention Name(s)
perivascular vasopresssin-vaginal misprostol
Intervention Description
20 units diluted in 100mL of Normal Saline injected laparoscopic needle and misoprostol 400 mcg
Primary Outcome Measure Information:
Title
Operative Blood Loss
Description
The amount of blood loss during robotic assisted laparoscopic myomectomy
Time Frame
0 hours up to 24 hours
Secondary Outcome Measure Information:
Title
Total Operative Time
Description
Total time of the robotic assisted laparoscopic myomectomy
Time Frame
0 hours up to 24 hours
Title
Side Effects
Description
Side Effect profile for Misoprostol Use
Time Frame
0 hours up to 24 hours

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Reproductive aged women between in ages of 18 to 55 undergoing robotic assisted laparoscopic myomectomy. Exclusion Criteria: History of adverse reaction or allergy to Vasopressin. History of adverse reaction or allergy to Misoprostol. Medical contraindication to use of Vasopressin or Misoprostol Suspicion of possible reproductive cancer with contraindication of morcellation of uterine tissue. Significant medical condition or laboratory result that in the opinion of the Investigator indicate an increased vulnerability to study subject which exposes the subject to an unreasonable risk as a result of participating. Any clinically significant even or condition uncovered during the surgery, such as excessive bleeding or decompensation, that might render the subject medically unstable to continue the study or complicate the subject's intraoperative or postoperative course. Pregnant women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mary Ann H Son, M.D.
Phone
718 741 7100
Email
sonmaryann@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Pedram Bral, M.D.
Phone
718 741 7100
Email
pbral@maimonidesmed.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pedram Bral, M.D.
Organizational Affiliation
Maimonides Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maimonides Medical Center
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11219
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mary Ann H Son, M.D.
Phone
718-741-7100
Email
sonmaryann@gmail.com
First Name & Middle Initial & Last Name & Degree
Sara Meeder
Phone
718 283 7253
Email
smeeder@maimonidesmed.org
First Name & Middle Initial & Last Name & Degree
Lily N Shamsnia, M.D.
First Name & Middle Initial & Last Name & Degree
Mary Ann H Son, M.D.
First Name & Middle Initial & Last Name & Degree
Pedram Bral, M.D.

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD will not be shared.
Citations:
PubMed Identifier
26041328
Citation
Iavazzo C, Mamais I, Gkegkes ID. Use of misoprostol in myomectomy: a systematic review and meta-analysis. Arch Gynecol Obstet. 2015 Dec;292(6):1185-91. doi: 10.1007/s00404-015-3779-x. Epub 2015 Jun 4.
Results Reference
result
PubMed Identifier
21485725
Citation
Kalogiannidis I, Xiromeritis P, Prapas N, Prapas Y. Intravaginal misoprostol reduces intraoperative blood loss in minimally invasive myomectomy: a randomized clinical trial. Clin Exp Obstet Gynecol. 2011;38(1):46-9.
Results Reference
result
PubMed Identifier
7026295
Citation
Buttram VC Jr, Reiter RC. Uterine leiomyomata: etiology, symptomatology, and management. Fertil Steril. 1981 Oct;36(4):433-45. doi: 10.1016/s0015-0282(16)45789-4.
Results Reference
result
PubMed Identifier
27362908
Citation
Cohen SL, Senapati S, Gargiulo AR, Srouji SS, Tu FF, Solnik J, Hur HC, Vitonis A, Jonsdottir GM, Wang KC, Einarsson JI. Dilute versus concentrated vasopressin administration during laparoscopic myomectomy: a randomised controlled trial. BJOG. 2017 Jan;124(2):262-268. doi: 10.1111/1471-0528.14179. Epub 2016 Jun 30.
Results Reference
result
PubMed Identifier
25125317
Citation
Kongnyuy EJ, Wiysonge CS. Interventions to reduce haemorrhage during myomectomy for fibroids. Cochrane Database Syst Rev. 2014 Aug 15;2014(8):CD005355. doi: 10.1002/14651858.CD005355.pub5.
Results Reference
result
Links:
URL
https://www.fda.gov/Drugs/DrugSafety/default.htm
Description
FDA website

Learn more about this trial

Combined Vaginal Misoprostol and Perivascular Vasopressin

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