Acupuncture for Pain Relief During Induced Labour in Nulliparae: a Randomised Controlled Study
acupuncture
Neurologic Manifestations+1
+ Pain
+ Signs and Symptoms
Treatment Study
Summary
Study start date: August 1, 2005
Actual date on which the first participant was enrolled.This study focuses on first-time pregnant women who are having their labor induced due to a prolonged pregnancy or mild high blood pressure. The main goal is to explore the potential of acupuncture as a method for pain relief during this process. The study is important as it aims to find alternative ways to manage labor pain, which could potentially reduce the need for epidural analgesia, a common form of pain relief during childbirth that involves injecting medication into the lower back. The study involves four groups, each managed differently. One group receives manual acupuncture, another receives electro acupuncture, the third group receives sham acupuncture, and the last group receives no treatment. Manual and electro acupuncture involve the insertion of thin needles into specific points on the body, with electro acupuncture also using a mild electric current. Sham acupuncture mimics the process but without actual needle insertion. The study's primary outcome is to measure the rate of epidural analgesia administered during labor, which will help evaluate the effectiveness of acupuncture in managing labor pain.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.105 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * nulliparae * having labour induced for prolonged pregnancy or mild hypertension * no previous experience of acupuncture * give written informed consent Exclusion Criteria: * all who do not meet the inclusion criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
33.333% chance of being blinded to the placebo group
Treatment Groups
Group I
ShamGroup II
ExperimentalGroup III
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location