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Clinical Trial Summary

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


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05175079
Study type Interventional
Source Universiti Kebangsaan Malaysia Medical Centre
Contact
Status Completed
Phase N/A
Start date October 1, 2016
Completion date August 31, 2017

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