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Tampostat for Management of Postpartum Hemorrhage

Primary Purpose

Postpartum Hemorrhage

Status
Terminated
Phase
Phase 1
Locations
Bangladesh
Study Type
Interventional
Intervention
Tampostat
Condom catheter tamponade
Sponsored by
International Centre for Diarrhoeal Disease Research, Bangladesh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postpartum Hemorrhage focused on measuring Tampostat, Tamponade, Postpartum hemorrhage

Eligibility Criteria

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

Inclusion Criteria:

  1. Women who delivered their baby at the site hospital, or attended the site hospital with PPH that started within the last 24 hours.
  2. Women with primary PPH have received AMTSL.
  3. PPH is due to atonic uterus.
  4. Provides written informed consent for enrolment in the study.

Exclusion Criteria:

  1. Primary PPH caused by retained placenta or ruptured uterus.
  2. Women who delivered before 28 weeks of gestation.
  3. Women not willing to participate in the study.

Sites / Locations

  • Obstetrical Ward of Shaheed Suhrawardi Medical College Hospital (ShSMCH) and Dhaka Medical College Hospital (DMCH)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Tampostat

Condom catheter tamponade

Arm Description

Tampostat™ is a self-regulating, low cost, pressure based emergency obstetric device designed specifically for use in low-resource settings. It has 6 parts: probe, condom, O ring, nerve centre, tube and bulb pump. It offers significant benefits over the current model by simplifying the insertion process, reducing the need for constant monitoring, eliminating leakage and the need for sterile saline, and using a pressure-based mechanism to apply consistent pressure to all women regardless of uterus size.Women who develop PPH even after applying AMTSL at the hospital or women who visit the hospital with PPH within 24 hours after delivery will be managed by Tampostat for the intervention arm or by the condom catheter tamponade in the control arm(172 patients in each arm)

Condom catheter tamponade have been used by medical professionals for several years in the management of atonic (primary) PPH. In this approach, Sterile rubber catheter fitted with a condom as a tamponade balloon device and using normal saline to inflate the condom.

Outcomes

Primary Outcome Measures

Safety of Tampostat as measured by number of serious adverse events in primary PPH management
The safety of Tampostat [no. of Serious adverse events i.e. Incidence of air embolism, injury to the uterine wall, pain during inflation of condom & continuation of vaginal /uterine bleeding during use of Tampostat] in primary PPH management.
Efficacy of Tampostat as measured by number of successful cases in arresting bleeding in Primary PPH
Efficacy [number of successful cases in arresting bleeding due to primary PPH from atonic uterus] of Tampostat in the management of primary postpartum hemorrhage (PPH)
Comparison of the efficacy of Tampostat as measured by number of successful cases in arresting primary PPH and the time takes to arrest the bleeding with that of the condom catheter tamponade
Comparison of the efficacy of Tampostat in terms of arresting primary PPH due to atonic uterus with that of the conventional condom catheter tamponade [no. of successful cases in arresting primary post partum bleeding using Tampostat and condom catheter and the time both takes to arrest the bleeding]

Secondary Outcome Measures

Feasibility as measured by number of physicians consider Tampostat as a feasible device in arresting primary PPH
The feasibility of Tampostat[number of physicians consider Tampostat as a feasible device in arresting primary PPH due to atonic uterus] in the management of primary PPH by
Applicability of Tampostat as measured by rating by service providers using pre established scoring system in the management of primary PPH
Applicability[rating by service providers on applicability of the device using pre established scoring system]of Tampostat in the management of primary PPH due to atonic uterus.

Full Information

First Posted
March 16, 2015
Last Updated
November 22, 2018
Sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Collaborators
Grand Challenges Canada, Jibon Health Technologies, Inc., Shaheed Suhrawardi Medical College Hospital, Dhaka Medical College
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1. Study Identification

Unique Protocol Identification Number
NCT02416089
Brief Title
Tampostat for Management of Postpartum Hemorrhage
Official Title
Tampostat: A Low-cost, Self-regulating Tamponade for Management of Postpartum Hemorrhage in Bangladesh
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Terminated
Study Start Date
April 2015 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
December 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Collaborators
Grand Challenges Canada, Jibon Health Technologies, Inc., Shaheed Suhrawardi Medical College Hospital, Dhaka Medical College

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to evaluate the safety, feasibility and applicability of a new device 'Tampostat' in the management of primary postpartum hemorrhage and compare the efficacy of 'Tampostat' in terms of arresting primary PPH with that of the conventional condom catheter.
Detailed Description
This will be a 2-year study having two parts. Part A will be a Proof of Concept (POC) study that will be conducted at the Obstetrical Ward of Shaheed Suhrawardi Medical College Hospital (ShSMCH) and Dhaka Medical College Hospital (DMCH). There is no sample size estimation of this POC study that will assess safety, feasibility and applicability of using Tampostat on 5 consenting women with PPH for each hospital. Part B of the study will be an open label, randomized clinical trial that will be conducted at the Obstetrical Ward of Dhaka Medical College Hospital (DMCH). In this part, 344 consenting women with primary PPH will be enrolled, and allocated to either Tampostat or the control intervention in equal numbers per randomization (172 patients in each arm). In both these parts, Tampostat will be used only when Active Management of Third Stage of Labour (AMTSL) has failed to prevent PPH within 24 hours after delivery. All the doctors involved in the provision of care and treatment to PPH patients will be trained on the WHO's standard of care; they will also receive training on appropriate use of the devices to be used in this trial. An expert committee constituted of OBGYN professionals, clinical trial specialists, and statisticians will oversee the technical management of patients, data collection and their procedures, and ethical issues in this trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postpartum Hemorrhage
Keywords
Tampostat, Tamponade, Postpartum hemorrhage

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
344 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tampostat
Arm Type
Experimental
Arm Description
Tampostat™ is a self-regulating, low cost, pressure based emergency obstetric device designed specifically for use in low-resource settings. It has 6 parts: probe, condom, O ring, nerve centre, tube and bulb pump. It offers significant benefits over the current model by simplifying the insertion process, reducing the need for constant monitoring, eliminating leakage and the need for sterile saline, and using a pressure-based mechanism to apply consistent pressure to all women regardless of uterus size.Women who develop PPH even after applying AMTSL at the hospital or women who visit the hospital with PPH within 24 hours after delivery will be managed by Tampostat for the intervention arm or by the condom catheter tamponade in the control arm(172 patients in each arm)
Arm Title
Condom catheter tamponade
Arm Type
Active Comparator
Arm Description
Condom catheter tamponade have been used by medical professionals for several years in the management of atonic (primary) PPH. In this approach, Sterile rubber catheter fitted with a condom as a tamponade balloon device and using normal saline to inflate the condom.
Intervention Type
Device
Intervention Name(s)
Tampostat
Intervention Type
Device
Intervention Name(s)
Condom catheter tamponade
Primary Outcome Measure Information:
Title
Safety of Tampostat as measured by number of serious adverse events in primary PPH management
Description
The safety of Tampostat [no. of Serious adverse events i.e. Incidence of air embolism, injury to the uterine wall, pain during inflation of condom & continuation of vaginal /uterine bleeding during use of Tampostat] in primary PPH management.
Time Frame
2 months
Title
Efficacy of Tampostat as measured by number of successful cases in arresting bleeding in Primary PPH
Description
Efficacy [number of successful cases in arresting bleeding due to primary PPH from atonic uterus] of Tampostat in the management of primary postpartum hemorrhage (PPH)
Time Frame
12 months
Title
Comparison of the efficacy of Tampostat as measured by number of successful cases in arresting primary PPH and the time takes to arrest the bleeding with that of the condom catheter tamponade
Description
Comparison of the efficacy of Tampostat in terms of arresting primary PPH due to atonic uterus with that of the conventional condom catheter tamponade [no. of successful cases in arresting primary post partum bleeding using Tampostat and condom catheter and the time both takes to arrest the bleeding]
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Feasibility as measured by number of physicians consider Tampostat as a feasible device in arresting primary PPH
Description
The feasibility of Tampostat[number of physicians consider Tampostat as a feasible device in arresting primary PPH due to atonic uterus] in the management of primary PPH by
Time Frame
2 months
Title
Applicability of Tampostat as measured by rating by service providers using pre established scoring system in the management of primary PPH
Description
Applicability[rating by service providers on applicability of the device using pre established scoring system]of Tampostat in the management of primary PPH due to atonic uterus.
Time Frame
2 months

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women who delivered their baby at the site hospital, or attended the site hospital with PPH that started within the last 24 hours. Women with primary PPH have received AMTSL. PPH is due to atonic uterus. Provides written informed consent for enrolment in the study. Exclusion Criteria: Primary PPH caused by retained placenta or ruptured uterus. Women who delivered before 28 weeks of gestation. Women not willing to participate in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aminur Rahman, MBBS,MSc
Organizational Affiliation
International Centre for Diarrhoeal Disease Research, Bangladesh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Obstetrical Ward of Shaheed Suhrawardi Medical College Hospital (ShSMCH) and Dhaka Medical College Hospital (DMCH)
City
Dhaka
Country
Bangladesh

12. IPD Sharing Statement

Citations:
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12681884
Citation
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Seligman, B. and X. Liu, Economic assessment of interventions for reducing postpartum hemorrhage in developing countries. 2006: Abt Associates.
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Tampostat for Management of Postpartum Hemorrhage

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