Caesarian Section Clinical Trial
Official title:
Comparison of Successful Spinal Needle Insertion Between Obese and Non-obese Pregnant Women in Crossed Leg Sitting Position Undergoing Caesarean Section
Verified date | February 2017 |
Source | Indonesia University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study aimed to compare successful spinal needle insertion between obese and non-obese pregnant women in crossed leg sitting position undergoing cesarean section
Status | Completed |
Enrollment | 136 |
Est. completion date | December 2016 |
Est. primary completion date | August 2016 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Subjects aged 18-45 years old, with American Society of Anesthesiologists (ASA) physical status I-III who were planned to undergo caesarian section with spinal anesthesia in crossed leg sitting position. - Subjects have been explained about the study, have agreed to enroll and have signed the informed consent form Exclusion Criteria: - Subjects with contraindications for spinal anesthesia - Subjects with fetal's head trapped, umbilical prolapse, and foot presentation - Subjects with pre-eclampsia - Subjects with cardiovascular diseases - Subjects with scoliosis - Subjects with recent lumbal surgery history - Subjects who cannot sit in crossed leg sitting position. Drop out criteria: - Subjects with worsening conditions before spinal anesthesia - Subjects with failed spinal needle insertion and thus received general anesthesia - Subjects with twin pregnancy - Subjects drop out the study. |
Country | Name | City | State |
---|---|---|---|
Indonesia | Cipto Mangunkusumo Central National Hospital | Central Jakarta | DKI Jakarta |
Indonesia | Cipto Mangunkusumo Cental National Hospital | Jakarta | DKI Jakarta |
Lead Sponsor | Collaborator |
---|---|
Indonesia University |
Indonesia,
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of successful spinal needle placement in the first attempt | The number of successful spinal needle placement in the first attempt was recorded in yes/no method. | 2 months | |
Primary | The number of needle-bone contact | The number of spinal needle-bone contact | 2 months | |
Secondary | The number of blood vessel puncture incidence. | The number of blood vessel puncture incidence by the spinal needle during insertion. | 2 months |
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