Two-Drug combo tested to stop Post-Surgery nausea
NCT ID NCT07813897
First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
Researchers test whether combining palonosetron and dexamethasone prevents postoperative nausea and vomiting better than palonosetron alone. The trial enrolls 76 women aged 20 to 40 undergoing gynaecological laparoscopic surgery. Participants receive either the combination or palonosetron alone before anaesthesia, and researchers track nausea and vomiting episodes for 24 hours after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- palonosetron combined with dexamethasone
- What this could lead to
- If the combination works better, it could become a standard preventive approach for nausea and vomiting after gynaecological laparoscopic surgery.
- What could go wrong
- This is a small, single-center Phase 4 trial in a narrow group of healthy women. The results may not apply to other surgeries or patients with different risk factors.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
76 people
The number who actually took part.
- Started
-
Sep 2025
- Finished
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May 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
20 to 40 years
- Sex
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Female participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients undergoing gynaecological laparoscopic surgery * ASA physical status I and II * Age 20-40 years * Provided informed consent Exclusion Criteria: * Pregnancy * Menstruation * Gastroesophageal reflux disease * BMI \>35 kg/m² * Allergy or contraindication to study drug
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Bangladesh Medical University
Dhaka, 100, Bangladesh
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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