Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT03729089 |
| Other study ID # |
BPP-NSA-001 |
| Secondary ID |
|
| Status |
Completed |
| Phase |
N/A
|
| First received |
|
| Last updated |
|
| Start date |
November 1, 2018 |
| Est. completion date |
March 29, 2019 |
Study information
| Verified date |
April 2019 |
| Source |
St. Francis Hospital Nsambya |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
Study topic:
Predicting fetal outcome using third trimester modified biophysical profile (BPP) scan
compared with standard of care; a randomized clinical trial at St. Francis Hospital, Nsambya.
This is an open label randomized clinical trial comparing the third trimester modified
biophysical profile done between 34 to 40 weeks with the current standard of care in reducing
perinatal mortality at St. Francis Hospital, Nsambya
Objectives of the study:
Broad study objectives:
To evaluate the role of third trimester modified biophysical profile scan in predicting fetal
outcome among pregnant mothers at St. Francis Hospital, Nsambya.
Specific study objectives:
- To determine the percentage decline in perinatal mortality following use of third
trimester biophysical profile from 34 to 40 weeks at St. Francis Hospital, Nsambya.
- To determine if use of third trimester BPP scan improves prediction of perinatal outcome
more than the current standard of care at St. Francis Hospital, Nsambya.
- To determine the fetal outcome of pregnancies done modified BPP and those who received
current standard of care at St. Francis Hospital, Nsambya.
Hypothesis:
The hypothesis of the study is that performing third trimester modified biophysical profile
scan between 34 and 40 weeks compared to standard of care is associated with a 16 percent
reduction
Description:
Randomization:
Eligible participants will be randomly allocated to one of the two study groups (modified
biophysical profile scan arm or current standard of care arm) by an independent statistician
who will not be involved in data analysis. The independent statistician will generate a
randomization register consisting of the sequential study numbers but without the allocated
study group. The register will be held at the enrollment clinic and patients who will be
eligible for enrollment will be assigned the next available number on the register until the
required sample size is reached. The principal investigator will identify a secure room from
where opaque envelopes containing the different study arms will be kept. Participants will
pick envelopes randomly from the pool of envelopes to obtain the study arm to which they
automatically belong.
Blinding:
The study will be open label but only blinding the allocation at study entry.
Randomization concealment
No one including the independent statistician will know the study arm at the point of
randomization. Because the intervention is not blinded, the rest of the study team including
the principle investigator will get to know the study arm after the women have been
randomized.
Sample size:
The use of fetal biophysical profile has been associated with 61 to 79 percent reduction in
fetal mortality and morbidity. The incidence of perinatal death (Macerated still birth, Fresh
stillbirth & Early neonatal death) in 2016 was 2% of the annual total deliveries, giving a
perinatal mortality ratio of 20 per 1000 live birth at St. Francis Hospital Nsambya. The
following assumptions will be made in the determination of the minimum sample size; the
current standard of care of mothers attending antenatal care at Nsambya Hospital as defined
by World health organization (WHO) in 2016 will detect up to 79% of fetal outcome, while
performing modified biophysical profile scan proposed in this trial will increase this
proportion to 95% at the 5% level of significance, and power of 80. Using a formula for
comparing two proportions from Medical statistics book by Betty Kirkwood and Jonathan Sterne,
2003; The minimum sample size , Where this gives an increase in prediction of 16%. V= the
Standard normal deviate at 95% Confidence (from Z-statistical tables, V=1.96), U =Standard
Normal Deviate at 80% Power (power =1-β) ( from Z-statistical tables, u=0.84). Substituting,
= 89.2 women. This gives approximately 90 women in each group and a total sample size of 180
women. Assuming a non-response proportion of 10%, the sample size will be increased by 10% to
198 women (99 in each group).
Data management and handling:
The study data will be entered using Microsoft (MS) access (MS-ACCESS, 2016) and will be
double checked and validated before being uploaded into the database. The data entry screens
will incorporate a number of range checks and logical skips as appropriate. Data stored in
the database will be checked for missing or unusual values (range checks) and checked for
consistency within participants. If any such problems are identified the problematic
questionnaire will be returned to the clinic for checking and confirmation or correction, as
appropriate. The amended version will be returned to the data entrant for correct entry into
the database.
Statistical analysis plan:
Participant socio-demographics and other characteristics will be summarized using counts and
percentages and by study group, for categorical variables and means and standard deviation
for continuous variables. The analysis will be by intention to treat (ITT). I will calculate
the mortality rate as the number of death divided by total time of follow up. The mortality
will be further stratified by the study group (intervention vs standard of care). Rate ratio
comparing the trial groups will be estimated by fitting a cox regression model. If there are
any imbalance in the important participant characteristics at baseline, adjustment for these
will be performed by fitting cox regression models. A similar analysis will be performed for
the secondary outcomes.
Data quality control:
The study team will be trained on data collection and handling procedures. A pretest in form
of completing the study questionnaire as well as a dry run will be done before the
commencement of the actual data collection. To ensure proper data management, the data
collectors will be trained in data management and will complete certification process of Good
Clinical Practices (GCPs). Data collectors will be health workers who work in the Obstetrics
department, they will not be directly involved in the management of mothers in Antenatal
clinic or inpatient wards to avoid observation bias if he/she was among the people managing
these patients. All interviews will be conducted in the language understood by the study
participants.
Data monitoring committee:
There will be a data monitoring committee established to monitor the quality of data being
collected. This three member committee will be selected from outside the study site. They
will be people with experience in monitoring trial data. They will sit every 3 months or as
requested by the institutional review board of St. Francis Hospital Nsambya.
Data protection and confidentiality:
The study questionnaires will not bear participant names but rather identification numbers.
The study team will ensure the data is not accessible to anyone else by 1) keeping the paper
questionnaires under lock and key 2) using passwords to secure the study database. The team
will also ensure that the study data is used for only the purpose approved by the ethics
committees.
Ethical considerations:
The study will seek ethical approvals from the Institutional Review Board (IRB) of Nsambya
Hospital. The Hospital authority will also be requested for permission to have access to the
pregnant women in the study clinic. Participants will be allowed to withdraw from the study
whenever they so wish. All the data collected will be treated with utmost confidentiality.
STANDARD OPERATING PROCEDURE (SOP) FOR ENROLLMENT/SCREENING VISIT
1. The pregnant women are received, welcomed and briefed about the services by the midwife
in the Antenatal clinic registration desk.
2. The midwife registering at the reception will identify pregnant women who are between 34
to 40 weeks gestation.
3. If one is attending for the first time but within the gestational age of interest, then
the base line investigations will be done (Complete blood count, blood grouping, HIV,
Urinalysis, Gestational diabetes mellitus screening, Syphilis test and Hepatitis B
test).
4. For those who have been booked already, the study midwife will check the antenatal card
and results of the above. If any is missing, a request would be written and sample
taken.
5. Body weight and blood pressure will be measured at this point.
6. Immediately after receiving the antenatal card, the pregnant women will be directed to
the waiting area from where routine antenatal health education and information about the
study is given by one of the Antenatal clinic and study Midwives.
7. After providing information about the study, the study midwife will duly consent the
mother and assign the randomization number sequentially from the register to those who
volunteer to participate in the study.
8. The pregnant mother is accompanied by midwife to the study office (Room 9) from where
the PI will request the mother to randomly pick an opaque envelope from the
randomization pack to determine the study arm of this study participant.
9. The study arm will be known by the study team at this point and clearly documented in
the patient's antenatal card.
10. The enrolled mothers will be examined by the study doctor or midwives and findings
documented in the Antenatal card and Case report form (CRF).
11. The mothers in the modified Biophysical profile ARM will be required to undergo a
modified biophysical profile scanning free of charge and the results of the scan
documented in the CRF.
12. The mother will bring back the results of the scan and blood tests to the study doctor.
The study doctor will document the above results on the CRF. He will give an appropriate
follow up date and indicate the date for performing the next modified biophysical
profile (mBPP) scan.
13. The registers and all other documents are taken to the research office at the end of the
day by the Clinical Trial Midwife. All completed CRFs are scrutinized by the Trial PI
and signed. If the Trial midwife detects errors in the CRFs, He or she will put a Note
to the file accordingly as per the data management SOP.
14. The completed file folders will then be placed in the rack for not entered data. The
entry into the data base will then be as per the data management SOP.
STANDARD OPERATING PROCEDURE FOR MISSED VISITS
1. The pre-enrollment and enrollment registers will have the scheduled appointments for
each study participant.
2. Any study participant who fails to honor an appointment will be followed up with a phone
call the next day to ascertain the reason why she did not turn up and encouraged to
come. If she fails to turn up, a second phone call will be made and another appointment
fixed.
3. A study participant who fails to honor her appointments and fails to respond to the
above follow up would be considered as one lost to follow up.
STANDARD OPERATING PROCEDURE FOR TRACING MOTHERS WHO HAVE GONE PAST THEIR EXPECTED DATE OF
DELIVERY (EDD) / DELIVERED ELSEWHERE
1. Each week, mothers who have not delivered at the study site are traced from the CRF/date
of delivery list by the principle investigator.
2. The study participant is given a phone call and advised to visit the study site if not
delivered to see the Doctors to assess her and plan for her delivery. If the person has
already delivered from elsewhere, information regarding delivery is obtained and entered
into the CRF.
STANDARD OPERATING PROCEDURE FOR UNSCHEDULED VISIT
1. Participants will be encouraged to come in every time they have a problem direct to
Antenatal clinic Room 9 or labor ward in case it's after 5.00 pm where a doctor reviews
her and the clinical trial coordinator is informed.
2. Participant will be seen by the Clinical Trial Investigator in the Antenatal Clinic on
Monday- Friday from 8:00am-5:00pm.
3. After 5:00pm, during weekends, public holidays, Participant will report to the Labor
ward and be seen by the Doctor on Duty and managed appropriately.
STANDARD OPERATING PROCEDURE FOR DOCUMENTING DELIVERY AND FETAL OUTCOME
1. Identification of study Participants who present in labor ward will be done by any of
the labor ward midwives by asking for their antenatal card bearing the sticker and by
asking whether the participant has been in the study. This process will be for both
mothers in labor and those scheduled for Cesarean section.
2. The labor ward midwives will then inform one of the research midwives about the study
participant. The research midwife will then verify the antenatal records and place an
appropriate sticker on the patient file for easy identification. The study midwife will
duly inform the Principle investigator.
3. For mothers who will undergo an elective or emergency cesarean section, the birth
outcome will be documented from the post natal wards.
4. Immediately after delivery of the baby, the study midwife will document the birth
outcome in the CRF which placed in a box file awaiting data cleaning and entry.
5. The above procedure will be followed for delivery during day, night and over the
weekend.
STANDARD OPERATING PROCEDURE FOR DATA MANAGEMENT
1. The Case report form (CRF) will be assessed by the Clinical Trial Principle Investigator
daily for accuracy, legibility and completeness.
2. The CRFs will then be filled, placed in the respective file folder and then placed in
the rack for not entered data.
3. Only authorized study staffs (the Data Clerks, Principal Investigator, statisticians)
are allowed to have access to the database.
4. Every afternoon, the Data Clerk will pick the CRFs from the box file of not entered data
and then enter it into the database (Epi-data)
5. At the end of the day, all data will be saved and backed up on a flash disk or External
Hard Drive.
6. After the CRFs have been entered into the database, they will be placed in the Box file
for entered data for proper storage by one of the Data Clerks.
STANDARD OPERATING PROCEDURE FOR COMPLETING CASE REPORT FORM (CRF)
1. CFR must be filled with a ball-point-black ink.
2. Capital letters must be used in all entries of the CRF. The dates that are not known
will be represented with value 11/11/1111.
3. The Principle investigator and the Trial Coordinator will write Not applicable on all
different CRF for non obtainable information whether numerical or non numerical.
4. Corrections on CRF will be done by the person who has filled in that CRF.
5. Corrections will be done by crossing out the wrong entry with a single line, then
writing the correct entry alongside/above/under the wrong entry.
6. After correction, a date will be placed alongside the correction as well as the initials
of the Research staff.
7. A note to file will be placed on that page of the CRFs to explain the correction by the
Research staff and confirmed by the Principal investigator
