Hemostatic Effect of Intrauterine Instillation of Oxytocin in Hysteroscopic Myomectomy (oxytocin)
Primary Purpose
Leiomyoma
Status
Unknown status
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Oxytocin
sterile bacteriostatic water ampule
Sponsored by
About this trial
This is an interventional other trial for Leiomyoma focused on measuring Hysteroscopic Myomectomy
Eligibility Criteria
Inclusion Criteria:
- Symptomatic patient (Menorrhagia, recurrent pregnancy loss or infertility).
- 1 or 2 submucous uterine myoma diagnosed by ultrasound with a diameter less than 4 cm
- Myoma with FIGO 0 or 1.
- Body mass index less than 35.
Exclusion Criteria:
- Pregnancy
- Active pelvic infection
- history of bleeding disorder or patient on anti-coagulant.
- hepatic and renal diseases.
- history of ischemic heart disease.
- Patients with uterine structural abnormality or uterine septum.
- Present or history of cervical or uterine cancer.
- Preoperative administration of gonadotropin-releasing hormone analogues or danazol.
- Allergy to glycine.
- Patients with hypercoagulopathy.
Sites / Locations
- Ain shams university maternity hospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Group A (Oxytocin group):
Group B (Placebo group):
Arm Description
30 women will undergo a hysteroscopic myomectomy with the use of 10 IU of oxytocin for every 1000 ml of the distending medium (1,5% Glycine ).
30 women will undergo hysteroscopic myomectomy with the use of a sterile bacteriostatic water ampule in the distending medium (1,5% glycine).
Outcomes
Primary Outcome Measures
the change in hemoglobin level 24 hours after the procedure surgery
the change of hemoglobin postoperative to know the effect of oxytocin compared to placebo in reducing blood loss.
surgery compared to the pre-operative values to see if intrauterine instillation of oxytocin will reduce blood loss during hysteroscopic myomectomy
the change of hematocrit level 24 hour after the procedure
a follow up CBC is done 24 hour after the procedure to see the difference in hematocrit and know about the blood loss intraoperative
Secondary Outcome Measures
the surgeon rating of intraoperative bleeding and the visual field quality of operative view,
After completing the procedure, the surgeon will complete a record scale to document estimated blood loss, rating the bleeding (0: no bleeding, I; mild bleeding, II: moderate bleeding, III: severe bleeding, IV: severe bleeding with clots).
the duration of surgery, intraoperative
Success of hysteroscopic myomectomy depends on good visualization throughout the procedure, so, if oxytocin decrease blood loss intraoperative , the operation time will be reduced .
intraoperative and postoperative complications
there are some operative complications as uterine perforation , cervical tear and fluid overload also, there is some adverse effects of oxytocin as arrythmia, nausea, vomiting , hypotension and abdominal pain
the surgeon rating the visual field
After completing the procedure, the surgeon will document the clarity of visual field using 3 point scale as (poor, fair, good)
the volume of distension media used intraoperative
glycine 1,5% is used as a distention media during procedure, each solution contain 1000 ml . counting the number of solution used intraoperative to calculate the amount of distension media used.
Full Information
NCT ID
NCT04996498
First Posted
July 7, 2021
Last Updated
August 6, 2021
Sponsor
Ain Shams Maternity Hospital
Collaborators
Ain Shams University
1. Study Identification
Unique Protocol Identification Number
NCT04996498
Brief Title
Hemostatic Effect of Intrauterine Instillation of Oxytocin in Hysteroscopic Myomectomy
Acronym
oxytocin
Official Title
Hemostatic Effect of Intrauterine Instillation of Oxytocin in Hysteroscopic Myomectomy: A Randomized Double Blinded Control Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
April 15, 2021 (Actual)
Primary Completion Date
July 1, 2022 (Anticipated)
Study Completion Date
October 1, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams Maternity Hospital
Collaborators
Ain Shams 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
There is no previous study on the hemostatic effect of intrauterine instillation of oxytocin in hysteroscopic myomectomy. All previous studies focused on intravenous administration of oxytocin.
This trial may modify the surgical environment in hysteroscopic myomectomy by decreasing intraoperative bleeding to a degree that the amount of distention medium required for uterine distention will be reduced with a better visibility and shorter operation time.
The standard treatment of symptomatic myomas is hysterectomy for women who have completed childbearing period, and myomectomy for women who wish to preserve fertility hysteroscopic myomectomy currently is the gold standard minimally invasive procedure for the management of symptomatic submucous fibroids. Success of hysteroscopic myomectomy depends on good visualization throughout the procedure, via the correct distending pressure, continuous irrigation and the use of electrosurgery to control bleeding. Prolonged procedures that need continuous irrigation under high pressure are associated with higher risk of excessive fluid absorption and intravasation syndrome due to opened blood vessels within the myometrial, moreover, the thermal damage of the healthy tissues is increased with the use of the coagulation current.
Oxytocin receptors exist in the non-pregnant uterus but the concentration of the receptors is much lower than in pregnancy. this is why the clinical use of oxytocin outside of pregnancy is limited Oxytocin acts on oxytocin receptors in the myometrium and fibroid tissue leading to uterine contraction and constriction of uterine vasculature due to uterine contraction and vaso-constrictive effect of oxytocin thus reducing uterine perfusion and results in reducing intraoperative bleeding.
Detailed Description
Patients will be subjected to:
History taking: including personal history, menstrual and obstetric history, medical and surgical history, medications.
Clinical examination; General and local with special concern about:
Size and position of the uterus
Transvaginal ultrasound to determine the number, size, location of fibroids and evaluation of the myometrial free margin that is defined as the minimum thickness between the outer edge of the fibroid and the inner edge of uterine serosa.
Laboratory evaluation: All participants will have routine blood tests: Complete Blood Count (CBC), serum creatinine, viral markers, coagulation profile and liver function tests.
Surgical procedure:
Office hysteroscopy will be performed the day before the procedure with the use of a 2-9 mm telescope with continuous-flow sheath (Hopkins II telescope 30 degrees: Karl storz) to assess and confirm the fibroid location, its intracavitary portion and to exclude any associated uterine pathology).
Hysteroscopy will be performed in the early proliferative phase (postmenstrual) in dorsal lithotomy position under general anesthesia, cervical dilatation will be done with Hegar dilators then resection of the submucous fibroid using monopolar resectoscope using 1,5% glycine as a distension medium by single operator to avoid inter-observer variability.
The intervention group (oxytocin group) will receive 10 IU of oxytocin for every 1000 ml of the distending medium (1,5% Glycine). While in the control group a sterile bacteriostatic water ampule in the same form will be added to every 1000 ml of the distending medium (1,5% Glycine).
After completing the procedure, the surgeon will complete a record scale to document estimated blood loss, rating the bleeding (0: no bleeding, I; mild bleeding, II: moderate bleeding, III: severe bleeding, IV: severe bleeding with clots). Also will document the clarity of visual field using 3 point likert scale as (poor, fair, good).
Post operative settings:
the duration of surgery and the volume of injected media will be calculated and documented.
all patients will be subjected to postoperative hemoglobin 24 hours after the procedure, any intraoperative or postoperative complications will be documented
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leiomyoma
Keywords
Hysteroscopic Myomectomy
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled double blinded clinical trial.
Masking
ParticipantCare ProviderInvestigator
Masking Description
The allocation will be concealed in sealed, sequentially numbered, white envelopes which will be prepared by a statistician where the drug will be covered with adhesive tape and handed over to the data collector. each woman will collect the corresponding sealed envelope directly from the data collector and it will be opened just before application of the drug.
the surgeon, the assistant and the nurse performing the procedure and the patient will be blinded to the medication drug which will be used inside the distention medium.
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Group A (Oxytocin group):
Arm Type
Active Comparator
Arm Description
30 women will undergo a hysteroscopic myomectomy with the use of 10 IU of oxytocin for every 1000 ml of the distending medium (1,5% Glycine ).
Arm Title
Group B (Placebo group):
Arm Type
Placebo Comparator
Arm Description
30 women will undergo hysteroscopic myomectomy with the use of a sterile bacteriostatic water ampule in the distending medium (1,5% glycine).
Intervention Type
Drug
Intervention Name(s)
Oxytocin
Other Intervention Name(s)
syntocinon
Intervention Description
intrauterine Instillation of oxytocin in distention media used during Hysteroscopic Myomectomy
Intervention Type
Other
Intervention Name(s)
sterile bacteriostatic water ampule
Intervention Description
a placebo drug similar in shape to oxytocin ampules
Primary Outcome Measure Information:
Title
the change in hemoglobin level 24 hours after the procedure surgery
Description
the change of hemoglobin postoperative to know the effect of oxytocin compared to placebo in reducing blood loss.
surgery compared to the pre-operative values to see if intrauterine instillation of oxytocin will reduce blood loss during hysteroscopic myomectomy
Time Frame
preoperative and 24 hour postoperative
Title
the change of hematocrit level 24 hour after the procedure
Description
a follow up CBC is done 24 hour after the procedure to see the difference in hematocrit and know about the blood loss intraoperative
Time Frame
preoperative and 24 hour postoperative
Secondary Outcome Measure Information:
Title
the surgeon rating of intraoperative bleeding and the visual field quality of operative view,
Description
After completing the procedure, the surgeon will complete a record scale to document estimated blood loss, rating the bleeding (0: no bleeding, I; mild bleeding, II: moderate bleeding, III: severe bleeding, IV: severe bleeding with clots).
Time Frame
immediately postoperative
Title
the duration of surgery, intraoperative
Description
Success of hysteroscopic myomectomy depends on good visualization throughout the procedure, so, if oxytocin decrease blood loss intraoperative , the operation time will be reduced .
Time Frame
immediately postoperative
Title
intraoperative and postoperative complications
Description
there are some operative complications as uterine perforation , cervical tear and fluid overload also, there is some adverse effects of oxytocin as arrythmia, nausea, vomiting , hypotension and abdominal pain
Time Frame
intraoperative and within the first 24 hours postoperative
Title
the surgeon rating the visual field
Description
After completing the procedure, the surgeon will document the clarity of visual field using 3 point scale as (poor, fair, good)
Time Frame
immediately postoperative
Title
the volume of distension media used intraoperative
Description
glycine 1,5% is used as a distention media during procedure, each solution contain 1000 ml . counting the number of solution used intraoperative to calculate the amount of distension media used.
Time Frame
immediately postoperative
10. Eligibility
Sex
Female
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Symptomatic patient (Menorrhagia, recurrent pregnancy loss or infertility).
1 or 2 submucous uterine myoma diagnosed by ultrasound with a diameter less than 4 cm
Myoma with FIGO 0 or 1.
Body mass index less than 35.
Exclusion Criteria:
Pregnancy
Active pelvic infection
history of bleeding disorder or patient on anti-coagulant.
hepatic and renal diseases.
history of ischemic heart disease.
Patients with uterine structural abnormality or uterine septum.
Present or history of cervical or uterine cancer.
Preoperative administration of gonadotropin-releasing hormone analogues or danazol.
Allergy to glycine.
Patients with hypercoagulopathy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Amir Mahfouz, Master
Phone
01013759260
Email
amir.hamdy21@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Mahmoud Ghaleb, MD
Phone
01007212975
Email
Mahmoudghaleb203050@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
amir Mahfouz, Master
Organizational Affiliation
AinShams MH
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ain shams university maternity hospital
City
Cairo
State/Province
Abbasia
ZIP/Postal Code
11517
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amir Mahfouz, Master
Phone
01223266784
Email
Amir.hamdy21@gmail.com
First Name & Middle Initial & Last Name & Degree
Mahmoud Ghaleb, MD
Phone
01007212975
Email
Mahmoudghaleb203050@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
18063608
Citation
Di Spiezio Sardo A, Mazzon I, Bramante S, Bettocchi S, Bifulco G, Guida M, Nappi C. Hysteroscopic myomectomy: a comprehensive review of surgical techniques. Hum Reprod Update. 2008 Mar-Apr;14(2):101-19. doi: 10.1093/humupd/dmm041. Epub 2007 Dec 6.
Results Reference
background
PubMed Identifier
25767949
Citation
Vilos GA, Allaire C, Laberge PY, Leyland N; SPECIAL CONTRIBUTORS. The management of uterine leiomyomas. J Obstet Gynaecol Can. 2015 Feb;37(2):157-178. doi: 10.1016/S1701-2163(15)30338-8.
Results Reference
background
PubMed Identifier
21345435
Citation
Munro MG, Critchley HO, Broder MS, Fraser IS; FIGO Working Group on Menstrual Disorders. FIGO classification system (PALM-COEIN) for causes of abnormal uterine bleeding in nongravid women of reproductive age. Int J Gynaecol Obstet. 2011 Apr;113(1):3-13. doi: 10.1016/j.ijgo.2010.11.011. Epub 2011 Feb 22.
Results Reference
background
PubMed Identifier
1309835
Citation
Maggi M, Magini A, Fiscella A, Giannini S, Fantoni G, Toffoletti F, Massi G, Serio M. Sex steroid modulation of neurohypophysial hormone receptors in human nonpregnant myometrium. J Clin Endocrinol Metab. 1992 Feb;74(2):385-92. doi: 10.1210/jcem.74.2.1309835.
Results Reference
background
PubMed Identifier
27862855
Citation
Atashkhoei S, Fakhari S, Pourfathi H, Bilehjani E, Garabaghi PM, Asiaei A. Effect of oxytocin infusion on reducing the blood loss during abdominal myomectomy: a double-blind randomised controlled trial. BJOG. 2017 Jan;124(2):292-298. doi: 10.1111/1471-0528.14416. Epub 2016 Nov 15.
Results Reference
background
Links:
URL
https://doi.org/10.1016/j.jmig.2011.09.005
Description
practice guidelines for the diagnosis and management of submucous leiomyomas. Journal of minimally invasive gynecology,
Learn more about this trial
Hemostatic Effect of Intrauterine Instillation of Oxytocin in Hysteroscopic Myomectomy
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