Pain Relief by Applying TENS on Acupuncture Points During the First Stage of Labour
This trial is active, not recruiting.
|Condition||pain relief at first stage|
|Treatment||transcutaneous electrical nerve stimulation|
|Sponsor||Chang Gung Memorial Hospital|
|Start date||August 2002|
|End date||December 2003|
|Trial size||100 participants|
|Trial identifier||NCT00148577, NMRPG1159|
We aimed to establish the reduction of labor pain by applying TENS at acupuncture points during the first stage of labour, to assess their efficacy, and to ascertain their acceptability.
Female participants from 20 years up to 40 years old.
Inclusion Criteria: The inclusion criteria were: - Voluntary informed participation to the study - An initial wish to deliver without epidural analgesia - Planned vaginal childbirth (non-obstetrical complicated pregnancy) - Fetal vertex presentation - Term pregnancy (>37 weeks of gestation) - Apply at 1st stage of labour and excluded if cervical dilatation > 5 cm - Age between 20 and 40 years - Chinese speaking, capable to understand the study - No experience of pain relief by systemic or epidural anesthesia in previous delivery - No experience in acupuncture or TENS in other field - Had no heart disease nor using pace-maker. Exclusion Criteria: - Cervical dilatation > 5 cm - Experience of pain relief by systemic or epidural anesthesia in previous delivery - Experience in acupuncture or TENS in other field - Had heart disease or using pace-maker
|Official title||Pain Relief by Applying Transcutaneous Electrical Nerve Stimulation (TENS) on Acupuncture Points During the First Stage of Labour: a Randomised Controlled Trial|
|Principal investigator||An-Shine Chao, MD|
|Description||We conducted a double-blind, placebo-controlled randomised trial involving healthy parturient at term pregnancy using TENS on 4 acupuncture points (Li 4 and Sp 6) (n=50) and the placebo group (n=50). Visual analogue scale (VAS) was used to assess the effect on pain before the application, 30 minutes and 60 minutes after TENS. The objective parameter of outcome was the score of VAS decreased in each groups. A post-partum questionnaire was given 24 hours later to evaluate the satisfaction and the use of this pain relieving method for the next delivery.|
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