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Balloon Tamponade for Atonic Primary Postpartum Hemorrhage (UBT)

Primary Purpose

Postpartum Hemorrhage

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Bakri balloon
Condom loaded foley's catheter
Sponsored by
Assiut University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postpartum Hemorrhage focused on measuring condom-loaded Foley's catheter, Bakri balloon, primary atonic postpartum hemorrhage

Eligibility Criteria

20 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women who accept to participate (either the patient or her first-kin if she is unconscious)
  • Primary atonic postpartum hemorrhage

Exclusion Criteria:

  • Traumatic postpartum hemorrhage
  • With any suspected (e.g. prolonged rupture of membranes) or clinical evidence of infection
  • Pre eclampsia.
  • Diabetes mellietus(DM) with pregnancy
  • History of Deep venous thrombosis (DVT) or other thromboembolic complication
  • Rheumatic heart patients

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Bakri balloon group

    Condom loaded Foley's catheter group

    Arm Description

    The women in this group will be managed by Bakri balloon

    The women in this group will be managed by condom loaded Foley's catheter

    Outcomes

    Primary Outcome Measures

    Number of patients who need surgical intervention to stop the bleeding

    Secondary Outcome Measures

    Time between insertion and stoppage of bleeding (minutes)
    Number of patients who need a blood transfusion
    Number of patients who developed fever
    The amount of blood loss (ml) after application of the balloon
    Number of patients who referred to Intensive care unit
    Number of patients who developed disseminated intravascular coagulopathy
    Duration (minutes) of bleeding after deflation of the balloon
    amount of bleeding (ml) after deflation of the balloon

    Full Information

    First Posted
    March 24, 2015
    Last Updated
    November 20, 2017
    Sponsor
    Assiut University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02430155
    Brief Title
    Balloon Tamponade for Atonic Primary Postpartum Hemorrhage
    Acronym
    UBT
    Official Title
    Comparison of Condom-Loaded Foley's Catheter Versus Bakri Balloon for Treatment of Primary Postpartum Hemorrhage: A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    July 2014 (Actual)
    Primary Completion Date
    July 1, 2015 (Actual)
    Study Completion Date
    March 4, 2016 (Actual)

    3. Sponsor/Collaborators

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

    4. Oversight

    5. Study Description

    Brief Summary
    Postpartum hemorrhage (PPH) is responsible for around 25% of maternal mortality worldwide reaching as high as 60% in some countries.PPH can also be a cause of long-term severe morbidity, and approximately 12% of women who survive PPH will have severe anemia. Postpartum hemorrhage has been defined as blood loss in excess of 500 ml in a vaginal birth and in excess of 1 L in a cesarean delivery.For clinical purposes, any blood loss that has the potential to produce hemodynamic instability should be considered a PPH. However, clinical estimates of blood loss are often inaccurate. Primary (immediate) PPH occurs within the first 24 hours after delivery and approximately 70% of these cases are due to uterine atony. Furthermore, uterine tony is defined as the failure of the uterus to contract adequately after the child is born. Guidelines for the management of postpartum hemorrhage (PPH) involve a stepwise approach including the exclusion of retained products of conception and genital tract trauma. Uterine atony, which is the most common cause, the management of uterine atony is an established stepwise protocol that in many international guidelines. Uterine massage is recommended for the treatment of PPH. Initiate uterine massages soon as excessive bleeding/uterine atony is identified. Intravenous oxytocin alone still is the recommended uterotonic drug for the treatment of PPH. If intravenous oxytocin is unavailable or if the bleeding does not respond to oxytocin, intravenous ergometrine, oxytocin-ergometrine fixed dose or a prostaglandin drug (including sublingual misoprostol, 600 mcg) should be given. The use of intrauterine balloon tamponade is recommended for the treatment of primary PPH due to uterine atony in women who do not respond to uterotonics or if uterotonics are not available. Since 1983, when Goldrath published evidence that inserting a Foley catheter in the uterus and inflating it with water could achieve tamponade, case series and other studies have suggested that various uterine balloon tamponade(UBT) devices may be effective in treating PPH. The studies used various types of UBT devices, including a condom catheter, a Foley catheter, the Sengstaken-Blakemore Esophageal Tube, the Rusch Balloon, and the Bakri Uterine Balloon. In 2007, a systematic review of treatment options for PPH found that 84% success rate of UBT does not significantly vary from surgical treatment outcomes.The World Health Organization (WHO), the International Federation of Gynecology and Obstetrics (FIGO), the American College of Obstetricians and Gynecologists(ACOG), the Royal College of Obstetricians and Gynecologists(RCOG), and the International Confederation of Midwives (ICM) recognize balloon tamponade as a method that could significantly improve the management intractable PPH, especially in low-resource areas. In 2012, WHO updated the guidelines for the management of PPH and retained placenta to include: "The use of intrauterine balloon tamponade is recommended for the treatment of PPH due to uterine atony. This recommendation is now stronger than the previous guidelines. It can be used for women who do not respond to uterotonics or if uterotonics are not available. This procedure potentially can avoid surgery and is appropriate while awaiting transfer to a higher-level facility".Furthermore, FIGO included UBT as a recommended second-line intervention for the treatment of PPH in their updated guidelines issued in 2012. Bakri first published the concept of intrauterine balloon technology in the management of hemorrhage secondary to placenta praevia-accreta during caesarean section with or without bilateral hypo gastric arterial ligation.In 2006, the ACOG Practice Bulletin, published by the American College of Obstetricians and Gynecologists, made mention of the Bakri postpartum balloon for its specifically tailored design that enables conservative management of uterine bleeding in cases of uterine atony and other causes of PPH. The idea of using a condom as a balloon tamponade was first generated and evaluated in Bangladesh by Sayeba Akhter to fill a need and in response to the high cost of commercially available UBT devices.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Postpartum Hemorrhage
    Keywords
    condom-loaded Foley's catheter, Bakri balloon, primary atonic postpartum hemorrhage

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Bakri balloon group
    Arm Type
    Active Comparator
    Arm Description
    The women in this group will be managed by Bakri balloon
    Arm Title
    Condom loaded Foley's catheter group
    Arm Type
    Active Comparator
    Arm Description
    The women in this group will be managed by condom loaded Foley's catheter
    Intervention Type
    Device
    Intervention Name(s)
    Bakri balloon
    Intervention Description
    is a 100% silicone construction, dual channel balloon catheter specifically designed and approved by FDA for intrauterine placement in cases of PPH. The Bakri balloon contains no latex, and therefore can be safely used in patients with latex allergies
    Intervention Type
    Device
    Intervention Name(s)
    Condom loaded foley's catheter
    Intervention Description
    Under aseptic precautions a sterile rubber catheter was inserted within the condom and tied near the mouth of the condom by a silk thread.
    Primary Outcome Measure Information:
    Title
    Number of patients who need surgical intervention to stop the bleeding
    Time Frame
    1 year
    Secondary Outcome Measure Information:
    Title
    Time between insertion and stoppage of bleeding (minutes)
    Time Frame
    1 year
    Title
    Number of patients who need a blood transfusion
    Time Frame
    1 year
    Title
    Number of patients who developed fever
    Time Frame
    1 year
    Title
    The amount of blood loss (ml) after application of the balloon
    Time Frame
    1 year
    Title
    Number of patients who referred to Intensive care unit
    Time Frame
    1 year
    Title
    Number of patients who developed disseminated intravascular coagulopathy
    Time Frame
    1 year
    Title
    Duration (minutes) of bleeding after deflation of the balloon
    Time Frame
    1 year
    Title
    amount of bleeding (ml) after deflation of the balloon
    Time Frame
    1 year

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Women who accept to participate (either the patient or her first-kin if she is unconscious) Primary atonic postpartum hemorrhage Exclusion Criteria: Traumatic postpartum hemorrhage With any suspected (e.g. prolonged rupture of membranes) or clinical evidence of infection Pre eclampsia. Diabetes mellietus(DM) with pregnancy History of Deep venous thrombosis (DVT) or other thromboembolic complication Rheumatic heart patients

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    32609374
    Citation
    Kellie FJ, Wandabwa JN, Mousa HA, Weeks AD. Mechanical and surgical interventions for treating primary postpartum haemorrhage. Cochrane Database Syst Rev. 2020 Jul 1;7(7):CD013663. doi: 10.1002/14651858.CD013663.
    Results Reference
    derived

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    Balloon Tamponade for Atonic Primary Postpartum Hemorrhage

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