search
Back to results

Oxygen Therapy and Pregnancy in Sickle Cell Disease (DRO2G)

Primary Purpose

Sickle Cell Disease

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
oxygen therapy
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Sickle Cell Disease focused on measuring sickle cell disease, oxygen therapy, pregnancy, pregnancy in sickle cell disease

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Pregnant women from 18 to 50 years old
  • Maximal term: 20SA
  • Patient with sickle cell disease
  • Consent form signed by the patient
  • Affiliated or beneficiary of a health insurance regimen and State Medical Aid.

Exclusion Criteria:

  • Patients with transfusion restrictions
  • Patients whose house can not receive the device
  • Patients who have a weekly use of prophylactic oxygen therapy at home
  • Patients who don't understand the operating instructions *Include patients with a doctor's prescription only. The portable oxygen concentrator will be removed from patients' home at the initiation visit prior to the overnight home oximetry test.

Sites / Locations

  • Hôpital Necker Enfants-Malades (Public Hospitals of Paris)

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

control

oxygen therapy

Arm Description

standard medical care

Outcomes

Primary Outcome Measures

Occurrence of at least one vaso-occlusive complication which last more than 24h
Painful vaso-occlusive episodes in bones, acute chest syndrome, ischemic stroke, cardiomyopathy, pulmonary hypertension, splenic and hepatic sequestration, death of the mother

Secondary Outcome Measures

Occurrence of at least one vaso-occlusive complication which last more than 24h
Painful vaso-occlusive episodes in bones, acute chest syndrome, ischemic stroke, cardiomyopathy, pulmonary hypertension, splenic and hepatic sequestration, death of the mother
Occurrence of pregnancy-induced hypertension, pre-eclampsia, eclampsia
Occurence of hospitalisation because of premature delivery risk
Occurence of late miscarriage
Occurence of Preterm (<35SA) and very preterm ( from 26 to 32SA)
Type of delivery (vaginal, active, caesarean)
Number of days hospitalisation postpartum
Occurence of Neonatal complications ( respiratory distress, analgesics withdrawal symptom)
Number of days of hospitalisation for the newborn
Number of days of hospitalisation in resuscitation unit for the newborn
Newborn weight
Newborn size
Newborn head circumference
Apgar score assess 1 min after birth
Apgar score assess 5 min after birth
Apgar score assess 10 min after birth
Perinatal and neonatal death
pH of of the newborn
Lactate of of the newborn
Number of days using painkiller (level II and III) during pregnancy
Number of urgent consultation
Number of days of hospitalisation and hospitalisation in intensive care during pregnancy
Stage of pregnancy at the first transfusion
Total volume of transfusion during pregnancy
Way of transfusion: simple, bleeding-transfusion, erythrocytapheresis
Maternal, fetal and newborn tolerability of home-based oxygen therapy during pregnancy

Full Information

First Posted
June 23, 2016
Last Updated
November 4, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
search

1. Study Identification

Unique Protocol Identification Number
NCT02813850
Brief Title
Oxygen Therapy and Pregnancy in Sickle Cell Disease
Acronym
DRO2G
Official Title
Impact of Home-based Oxygen Therapy on Maternal and Fetal Complications, in Pregnant Women With Sickle Cell Disease. A Randomized Multi-center Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
October 5, 2016 (Actual)
Primary Completion Date
December 3, 2021 (Actual)
Study Completion Date
August 12, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to assess the efficiency of the preventive oxygen therapy on the occurrence of vaso-occlusive complications, which last more than 24 hours and require hospitalisation, in women with sickle cell disease.
Detailed Description
Sickle cell disease (SCD) corresponds to a group of inherited disorders with clinical manifestations resulting from the biochemical consequences of a single-base substitution of valine by glutamic acid at position 6 of the ß-hemoglobin (Hb) subunit (HbA [ß6val] to HbS [ß6glu]). When the oxygen tension is low, the solubility of HbS falls and the molecules polymerize. In turn, the intracellular formation of HbS polymers results in red blood cell (RBC) sickling. The aggregation of sickle cells is responsible for the vaso-occlusive crises (VOCs) that characterize SCD. Thanks to improvements in the management of SCD patients, over 95% of affected infants survive to adulthood. Pregnancy is a high-risk situation for women with sickle cell disease, especially in the third trimester, during delivery and in the post-partum period. Conversely sickle cell disease can lead to pregnancy complications for both mother and fetus since maternal-fetal mortality remains elevated. RBC transfusions and careful prevention of infections represent the only available treatments in this situation. The complexity of this setting and the associated therapeutic strategy is further accentuated by the high frequency of post-transfusion side effects during SCD pregnancies, can indirectly affect the newborn by inducing hypoxia, and may ultimately prevent the woman from receiving further transfusions (RCOG, 2015) (Tuck et al, 1983). Post-transfusion complications constitute negative prognostic factors that affect both the mother's health and fetal development and thus increase the risk of premature death. Another factor complicating the outcome of the pregnancy is the increase in oxygen demand in order to satisfy the increased metabolic requirements of the placenta and fetus. As the maternal oxygen reserve can be compromised during pregnancy for several reasons (such as the increased oxygen consumption, the SCD related anemia accentuated by the plasmatic increase), patients are particularly susceptible to hypoxemia - leading to the exacerbation of sickling events and SCD-related complications. (Hill & Pickinpaugh, 2008)(Thame et al, 2007)(Rathod et al, 2007a)(Cines et al, 1998)(Hassell, 2005)(Pantanowitz et al, 2000)(Rathod et al, 2007b) Moving from this observation, the first innovative approach introduced was the widespread use of prophylactic oxygen treatment at home. The rationale behind this change came from experiments on a murine model of SCD mice, in which a high-oxygen environment during pregnancy was associated with a lower prenatal fetal/maternal mortality rate (Ye et al, 2008). The absence of severe complications was also noticed in some women who could not be transfused (because of severe alloimmunization) and who were already receiving oxygen therapy at home before pregnancy. Then a preliminary retrospective study was performed to evaluate the clinical benefit of the widespread use of prophylactic oxygen treatment at home. It indicates that this innovative treatment is safe and seems to be associated with a significant decrease in the transfusion rate in SCD patients during pregnancy. These findings are encouraging, but they are preliminary and bias have to be taken into account. These results have to be confirmed by a randomized trial. The project aim is to assess preventive oxygen therapy impact on women with sickle cell disease, their fetal and their newborn. Firstly, investigators want to assess preventive home-based oxygen therapy efficacy for preventing vaso-occlusive complications which last 24 hours and require a hospitalization. Secondly, they want to assess oxygen therapy impact on prevention and characteristics of obstetrical complications, prevention of neonatal complications, fetal and newborn's characteristics, type of medical care, transfusion balance sheet, way of transfusion and maternal, fetal and newborn tolerability of home-based oxygen therapy during pregnancy. For this they propose to analyze 200 pregnant SCD women. 100 women in the first arm with standard medical care. 100 women in the second arm who will have home-based oxygen therapy early at night. This study will be performed in 9 French hospitals. Blood samples of SCD women and blood cord will be drawn to monitor red cell adherence protein expression and function and their mechanic and adhesive properties.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sickle Cell Disease
Keywords
sickle cell disease, oxygen therapy, pregnancy, pregnancy in sickle cell disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
178 (Actual)

8. Arms, Groups, and Interventions

Arm Title
control
Arm Type
No Intervention
Arm Description
standard medical care
Arm Title
oxygen therapy
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
oxygen therapy
Intervention Description
Oxygen therapy early in the night (2L/min) during 4hours per days
Primary Outcome Measure Information:
Title
Occurrence of at least one vaso-occlusive complication which last more than 24h
Description
Painful vaso-occlusive episodes in bones, acute chest syndrome, ischemic stroke, cardiomyopathy, pulmonary hypertension, splenic and hepatic sequestration, death of the mother
Time Frame
30 days postpartum
Secondary Outcome Measure Information:
Title
Occurrence of at least one vaso-occlusive complication which last more than 24h
Description
Painful vaso-occlusive episodes in bones, acute chest syndrome, ischemic stroke, cardiomyopathy, pulmonary hypertension, splenic and hepatic sequestration, death of the mother
Time Frame
30 days postpartum
Title
Occurrence of pregnancy-induced hypertension, pre-eclampsia, eclampsia
Time Frame
20 months
Title
Occurence of hospitalisation because of premature delivery risk
Time Frame
20 months
Title
Occurence of late miscarriage
Time Frame
20 months
Title
Occurence of Preterm (<35SA) and very preterm ( from 26 to 32SA)
Time Frame
20 months
Title
Type of delivery (vaginal, active, caesarean)
Time Frame
20 months
Title
Number of days hospitalisation postpartum
Time Frame
20 months
Title
Occurence of Neonatal complications ( respiratory distress, analgesics withdrawal symptom)
Time Frame
20 months
Title
Number of days of hospitalisation for the newborn
Time Frame
20 months
Title
Number of days of hospitalisation in resuscitation unit for the newborn
Time Frame
20 months
Title
Newborn weight
Time Frame
20 months
Title
Newborn size
Time Frame
20 months
Title
Newborn head circumference
Time Frame
20 months
Title
Apgar score assess 1 min after birth
Time Frame
20 months
Title
Apgar score assess 5 min after birth
Time Frame
20 months
Title
Apgar score assess 10 min after birth
Time Frame
20 months
Title
Perinatal and neonatal death
Time Frame
20 months
Title
pH of of the newborn
Time Frame
20 months
Title
Lactate of of the newborn
Time Frame
20 months
Title
Number of days using painkiller (level II and III) during pregnancy
Time Frame
20 months
Title
Number of urgent consultation
Time Frame
20 months
Title
Number of days of hospitalisation and hospitalisation in intensive care during pregnancy
Time Frame
20 months
Title
Stage of pregnancy at the first transfusion
Time Frame
20 months
Title
Total volume of transfusion during pregnancy
Time Frame
20 months
Title
Way of transfusion: simple, bleeding-transfusion, erythrocytapheresis
Time Frame
20 months
Title
Maternal, fetal and newborn tolerability of home-based oxygen therapy during pregnancy
Time Frame
20 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnant women from 18 to 50 years old Maximal term: 20SA Patient with sickle cell disease Consent form signed by the patient Affiliated or beneficiary of a health insurance regimen and State Medical Aid. Exclusion Criteria: Patients with transfusion restrictions Patients whose house can not receive the device Patients who have a weekly use of prophylactic oxygen therapy at home Patients who don't understand the operating instructions *Include patients with a doctor's prescription only. The portable oxygen concentrator will be removed from patients' home at the initiation visit prior to the overnight home oximetry test.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexandra BENACHI, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Laure JOSEPH, MD,PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marina CAVAZZANA, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Necker Enfants-Malades (Public Hospitals of Paris)
City
Paris
ZIP/Postal Code
75015
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Oxygen Therapy and Pregnancy in Sickle Cell Disease

We'll reach out to this number within 24 hrs