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The Relationship of Abdominal Circumference and Trunk Length With the Level of Spinal Anesthesia in Obstetric Patients
This study is currently recruiting participants.
Verified by National Taiwan University Hospital, May 2008
First Received: September 1, 2008   Last Updated: September 5, 2008   History of Changes
Sponsored by: National Taiwan University Hospital
Information provided by: National Taiwan University Hospital
ClinicalTrials.gov Identifier: NCT00748176
  Purpose

The body shape might have influence on the spinal level. In this research we plan to investigate the relationship of abdominal circumference, trunk length and the level of spinal anesthesia in obstetric patients during Cesarean section.


Condition Intervention
Obstetrics for C/S
Procedure: spinal anesthesia

MedlinePlus related topics: Anesthesia
U.S. FDA Resources
Study Type: Observational
Study Design: Prospective
Official Title: The Relationship of Abdominal Circumference and Trunk Length With the Level of Spinal Anesthesia in Obstetric Patients

Further study details as provided by National Taiwan University Hospital:

Estimated Enrollment: 30
Study Start Date: July 2008
Estimated Study Completion Date: June 2009
Estimated Primary Completion Date: June 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
A Procedure: spinal anesthesia
spinal anesthesia with bupivacaine

Detailed Description:

The level of spinal anesthesia in obstetric patients had been investigated in several studies. Increased cephalad spread of local anesthetics had been demonstrated with increased intra-abdominal pressure, changes in anteroposterior spinal curves and lumbar lordosis. Theoretically the body shape might have contribution to the above factors and might have influence on the spinal level. In this research we plan to investigate the relationship of abdominal circumference, trunk length and the level of spinal anesthesia in obstetric patients during Cesarean section. Only those C/S patients indicated and scheduled for spinal anesthesia will be observed. The spinal anesthesia will be performed as routine practice. This study will not change the clinical plan in any aspect. We will only passively record the abdominal circumference, trunk length and the level of spinal anesthesia and calculate the correlation between them.

  Eligibility

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Obstetric patients for C/S

Criteria

Inclusion Criteria:

  • Obstetric patients for C/S

Exclusion Criteria:

  • With major systemic diseases
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00748176

Contacts
Contact: Hui-Hsun Huang, MD, PhD 23123456 ext 5515 hhh@ntu.edu.tw

Locations
Taiwan
National Taiwan University Hospital Recruiting
Taipei, Taiwan
Contact: Hui-Hsun Huang, MD,PhD     23123456 ext 5515     hhh@ntu.edu.tw    
Principal Investigator: Hui-Hsun Huang, MD, PhD            
Sponsors and Collaborators
National Taiwan University Hospital
Investigators
Principal Investigator: Hui-Hsun Huang Department of anesthesiology, National Taiwan University Hospital
  More Information

No publications provided

Responsible Party: Department of Anesthesiology, National Taiwan University Hospital ( Hui-Hsun Huang, Visiting Staff )
Study ID Numbers: 200805027R
Study First Received: September 1, 2008
Last Updated: September 5, 2008
ClinicalTrials.gov Identifier: NCT00748176     History of Changes
Health Authority: Taiwan: Department of Health

Study placed in the following topic categories:
Central Nervous System Depressants
Anesthetics
Bupivacaine

Additional relevant MeSH terms:
Therapeutic Uses
Physiological Effects of Drugs
Central Nervous System Depressants
Anesthetics
Central Nervous System Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on May 07, 2009