Labor Pain Clinical Trial
— TENSOfficial title:
fMRI Measurements on the Effect of Transcutaneous Electrical Nerve Stimulation (TENS) on Acupuncture Points Verses Spontaneous Normal Vaginal Delivery to Relief of Labor Pain
Verified date | October 2008 |
Source | Chang Gung Memorial Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Taiwan: Institutional Review Board |
Study type | Observational |
The purposes of this study is to integrate the objective tests into the subjective test, visual analog score (VAS), for evaluation and further understanding of relieving labor pain by TENS application on acupuncture points in the first stage of labor.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | December 2010 |
Est. primary completion date | July 2008 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 20 Years to 40 Years |
Eligibility |
Inclusion Criteria: - an initial wish to deliver without epidural analgesia - primigravida - planned vaginal childbirth without obstetrical or non-obstetrical complications - fetal vertex presentation - term pregnancy (>37 weeks of gestation) - age between 20 and 40 years - no experience in acupuncture or TENS for other reasons - no previous poor obstetrical outcome (either maternal or fetal). For those subjects willing to have fMRI: This study will be carried out only on right-handed Chinese women under accompany by a family member. Exclusion Criteria: - psychiatric and neurologic disorders, - candidate for vaginal birth after cesarean (VBAC); and - head trauma with loss of conscious, - major medical illness e.g., pacemaker parturient. |
Observational Model: Case Control, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Taiwan | AS Chao | Gueishan | Tao-Yuan |
Lead Sponsor | Collaborator |
---|---|
Chang Gung Memorial Hospital |
Taiwan,
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