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Acupressure in Hyperemesis Gravidarum

N

National University of Malaysia (UKM)

Status

Completed

Conditions

Hyperemesis Gravidarum

Treatments

Other: Standard treatment hospital protocol
Device: Acupressure band

Study type

Interventional

Funder types

Other

Identifiers

NCT05175079
FF-2017-195

Details and patient eligibility

About

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

Full 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.

Enrollment

90 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Onset of vomiting before 16 weeks
  2. Vomiting at least 2 times per day
  3. Ketonuria on admission
  4. Mid stream urine specimen that did not indicate infection

Exclusion criteria

  1. Non viable pregnancy
  2. Molar pregnancy
  3. Overt clinical features of thyrotoxicosis
  4. Known case of medical illness that associated with nausea and vomiting
  5. Patient refusal or patients who are not able to give consent

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

90 participants in 2 patient groups, including a placebo group

Accupressure group
Experimental group
Description:
acupressure 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
Treatment:
Device: Acupressure band
Control group
Placebo Comparator group
Treatment:
Other: Standard treatment hospital protocol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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