Ten-Year Practice of Labor Pain Control in China
Information source: Nanjing Medical University
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Labor Pain
Intervention: CSEA with PCA (Procedure); CSEA with IBI (Procedure); EA with PCA (Procedure); EA with IBI (Procedure)
Phase: N/A
Status: Not yet recruiting
Sponsored by: Nanjing Medical University Official(s) and/or principal investigator(s): XiaoFeng Shen, MD, Study Chair, Affiliation: Nanjing Medical University
Overall contact: FuZhou Wang, MD, Phone: 86-25-84460777, Ext: 3301, Email: zfwang50@gmail.com
Summary
Since 1999, labor pain control has being performed in China, and the initial time of
analgesia is at the cervix >= 2 cm. Meanwhile, American Society of Obstetrics & Gynecology
recommended that the labor analgesia with neuraxial block should be performed at the cervix
>= 4 cm in 2002. After that, the threshold has been revised to at least >= 2 cm in 2006 by
the Society. However, in China, the practice of labor analgesia with neuraxial block has
being performed for over seven years. Up to now, the practice has being experienced during
this ten-year period at the cervix around 1 cm. The investigators hypothesized that labor
pain control in different stage had different characteristics and had different influence on
patients short- and long-lasting outcomes. This study is mainly to investigate different
labor analgesia procedures in different stage since the initial of the practice in 1999, and
assess their influence on the outcomes to display the trajectory of development of labor
analgesia in China of which might fit to the the whole process of the study of labor
analgesia throughout the world. All these were done by analyzing the data records since from
January 1999 to December 2008.
Clinical Details
Official title: A Ten-Year Practice of Labor Pain Control in China
Study design: Other, Retrospective
Primary outcome: Rate of cesarean delivery
Secondary outcome: Rate of instrument-assisted deliveryIndications of cesarean delivery Maternal Visual Analog Scale (VAS) rating of pain Duration of analgesia Maternal satisfaction with analgesia Maternal oral temperature Use of oxytocin after analgesia Low back pain at 3 months after vaginal delivery Breastfeeding success at 6 weeks after vaginal delivery Neonatal one-minute Apgar scale Neonatal five-minute Apgar scale Incidence of maternal side effects Umbilical-cord gases analysis
Eligibility
Minimum age: 18 Years.
Maximum age: 45 Years.
Gender(s): Female.
Criteria:
Inclusion Criteria:
- Parturients used labor analgesia
Exclusion Criteria:
- Following criteria were based on the records of information received from the ten-year
practice screened by investigators:
1. Chronic pain and psychiatric diseases records
2. Participants younger than 18 years or older than 45 years
3. Alcohol addictive or narcotic dependent patients were excluded for their
influence on the analgesic efficacy of the epidural analgesics
4. Subjects with a nonvertex presentation or scheduled induction of labor
5. Diagnosed diabetes mellitus and pregnancy-induced hypertension
6. Twin gestation and breech presentation
Locations and Contacts
FuZhou Wang, MD, Phone: 86-25-84460777, Ext: 3301, Email: zfwang50@gmail.com
Nanjing Maternal and Child Health Care Hospital, Nanjing, Jiangsu 210004, China
Additional Information
Starting date: January 2009
Ending date: May 2009
Last updated: October 20, 2008
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