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Comparison of Aprepitant with combinations of Dexamethasone-Ondansetron and Aprepitant-Dexamethasone-Ondansetron for preventing nausea and vomiting after gynecological laparoscopic surgery

The effect of Dexamethasone-Ondansetron versus oral Aprepitant versus Dexamethasone-Ondansetron-oral Aprepitant combination for prevention of postoperative nausea and vomiting in day-care gynecological laparoscopy- a Randomised clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/05/013879
Enrollment
105
Registered
2018-05-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- 1. adults between 20-50 years age 2. those undergoing day-care gynecological laparoscopy 3. ASA class 1-2

Interventions

Intervention1: Aprepitant: To prevent post-operative nausea and vomiting 80 mg aprepitant capsule is given per oral 1 hour before surgery Intervention2: Aprepitant-Dexamethasone-Ondansetron-: To prev

Sponsors

Jawaharlal Institute of Postgraduate Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. female patients aged 20-50 years 2. ASA class 1 or 2 3. procedure- gynecological laparoscopy

Exclusion criteria

Exclusion criteria: 1. cardiovascular, respiratory, gastrointestinal diseases, diabetes 2. previous history of postoperative nausea and vomiting 3. pre-operative use of antiemetics or opioids 4. pregnancy 5. allergy to any of the three drugs under study 6. NPO inadequate

Design outcomes

Primary

MeasureTime frame
To compare the incidence and severity of postoperative nausea and vomiting after day-care gynecological laparoscopy following triple therapy with aprepitant,ondansetron and dexamethasone, when compared to oral aprepitant alone and ondansetron-dexamethasone combinationTimepoint: Nausea and vomiting will be noted immediately after extubation and post-operatively at 1st hour,2nd hour, 3rd hour and 4th hour

Secondary

MeasureTime frame
Duration from surgery to DischargeTimepoint: Within 24 hrs

Countries

India

Contacts

Public ContactDr Ingilala Lakshmi Thanuja

Jawaharlal Institute of Postgraduate Medical Education and Research

jipmersatyen@gmail.com9940973502

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026