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The Effect of Dimenhydrinate on Postoperative Nausea and Vomiting After Abdominal Hysterectomy: Randomized-controlled Trial

The Effect of Dimenhydrinate on Postoperative Nausea and Vomiting After Abdominal Hysterectomy: Randomized-controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06395064
Enrollment
160
Registered
2024-05-01
Start date
2024-05-01
Completion date
2026-04-30
Last updated
2024-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gynecologic Neoplasm, Healthy Women

Keywords

post-operative nausea vomiting

Brief summary

The aim of this clinical trial is to learn if Dimenhydrinate works to prevent postoperative nausea-vomiting in adult women who undergoing abdominal hysterectomy. The primary question is: Does Dimenhydrinate lower the proportion of postoperative nauseavomiting during the day 1 after surgery. Researcher will compare Dimenhydrinate to a placebo (a-look-alike substance that contains no drug) which will give intravenously when the patient come back to the ward, to see if Dimenhydrinate work to prevent nauseavomiting during the postoperative day1. All participants will receive standard treatment during pre-operative, intra-operative and the immediate post-operative periods. Participants will receive Dimenhydrinate or placebo only one dose after discharge from the recovery room. During the day 1 postoperative, participants will report their symptoms and keep a diary of the number of tmes they use additional anti-emetic drugs.

Interventions

Dimenhydrinate 50mg intravenously

Sponsors

Preeyaporn Jirakittidul
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-65 years female * undergoing trans abdominal hysterectomy

Exclusion criteria

* undergoing emergency surgery * pregnancy or breastfed women * post delivery less than 6 weeks * history of allergic reaction or precaution to use the protocol drug * BMI less than 18 or more than 30 kg/m2 * Need ICU care after surgery

Design outcomes

Primary

MeasureTime frame
occurrence and times of nausea vomitingat ward, 6, 12, 24 hr postoperation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026