Trial Outcomes & Findings for Severing Nuchal Cord at the Time of Delivery. (NCT NCT00345254)
NCT ID: NCT00345254
Last Updated: 2017-05-11
Results Overview
Recruitment status
COMPLETED
Study phase
NA
Target enrollment
60 participants
Primary outcome timeframe
immediately after delivery
Results posted on
2017-05-11
Participant Flow
Participant milestones
| Measure |
Severing Cord
The cord was cut intentionally after delivery of the anterior shoulder and prior to extraction of the body.
severing cord: The cord was cut intentionally after delivery of the anterior shoulder and prior to extraction of the body.
|
Untouched Cord
The cord was untouched after delivery of the anterior shoulder and prior to extraction of the body.
|
|---|---|---|
|
Overall Study
STARTED
|
30
|
30
|
|
Overall Study
COMPLETED
|
30
|
30
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Severing Nuchal Cord at the Time of Delivery.
Baseline characteristics by cohort
| Measure |
Severing Cord
n=30 Participants
The cord was cut intentionally after delivery of the anterior shoulder and prior to extraction of the body.
severing cord: The cord was cut intentionally after delivery of the anterior shoulder and prior to extraction of the body.
|
Untouched Cord
n=30 Participants
The cord was untouched after delivery of the anterior shoulder and prior to extraction of the body.
|
Total
n=60 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=5 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=5 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
30 Participants
n=5 Participants
|
30 Participants
n=7 Participants
|
60 Participants
n=5 Participants
|
|
Age, Categorical
>=65 years
|
0 Participants
n=5 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=5 Participants
|
|
Sex: Female, Male
Female
|
30 Participants
n=5 Participants
|
30 Participants
n=7 Participants
|
60 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
0 Participants
n=5 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=5 Participants
|
|
Region of Enrollment
Israel
|
30 participants
n=5 Participants
|
30 participants
n=7 Participants
|
60 participants
n=5 Participants
|
PRIMARY outcome
Timeframe: immediately after deliveryOutcome measures
| Measure |
Severing Cord
n=30 Participants
The cord was cut intentionally after delivery of the anterior shoulder and prior to extraction of the body.
severing cord: The cord was cut intentionally after delivery of the anterior shoulder and prior to extraction of the body.
|
Untouched Cord
n=30 Participants
The cord was untouched after delivery of the anterior shoulder and prior to extraction of the body.
|
|---|---|---|
|
Umbilical Cord pH
|
7.29 pH
Standard Deviation 0.07
|
7.32 pH
Standard Deviation 0.06
|
Adverse Events
Severing Cord
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Untouched Cord
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place