Clinical Trials Directory

Trials / Completed

CompletedNCT05175079

Acupressure in Hyperemesis Gravidarum

A Randomised Controlled Trial On Effect Of Acupressure On Nausea And Vomiting In Women With Hyperemesis Gravidarum

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Universiti Kebangsaan Malaysia Medical Centre · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

To examine the degree of nausea, vomiting between the acupressure and control group in women with hyperemesis gravidarum

Detailed description

A prospective RCT conducted at Department of Obst and Gynae, UKMMC. All pregnant women with a normal intrauterine pregnancy of ≤ 16 week gestation with hyperemesis gravidarum will be assessed by the medical officer/ specialist/ consultant in charge. Explanation regarding the research study will be given for patients who fulfill the inclusion and exclusion criteria. Patients who have understood the research study and consented will be recruited as subjects for the study.

Conditions

Interventions

TypeNameDescription
DEVICEAcupressure bandacupressure band apply to P6 (nei guan) point which located three fingers below the skin wrinkles of the anterior wrist. Acupressure band wear 3 times daily before breakfast, lunch and dinner for at least 10 minutes
OTHERStandard treatment hospital protocolIntravenous metaclopromide 10mg PRN Intravenous fluids as per protocol

Timeline

Start date
2016-10-01
Primary completion
2017-08-31
Completion
2017-08-31
First posted
2022-01-03
Last updated
2022-01-03

Locations

1 site across 1 country: Malaysia

Source: ClinicalTrials.gov record NCT05175079. Inclusion in this directory is not an endorsement.