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A clinical trial to compare two different drug schedules used for prevention of post-operative nausea and vomiting in patients undergoing total abdominal hysterectomy

To study efficacy of Dexamethasone and Palonosetron versus Promethazine and Palonosetron as prophylaxis of post-operative nausea and vomiting in patients undergoing abdominal hysterectomy under regional anaesthesia: A randomized single blind study - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056041
Enrollment
160
Registered
2023-08-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system Health Condition 2: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system

Interventions

Intervention1: Dexamethasone and Palonosetron: Dexamethasone 4mg intravenous at the time of induction and 0.075mg Palonosetron intravenous at time of wound closure Control Intervention1: Promethazine

Sponsors

Prashant Dhatwalia
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Duration of surgery exceeding 1 hour 2. BMI 3. ASA physical status grade I and II. 4. Nonsmoker.

Exclusion criteria

Exclusion criteria: 1. Patients with gastrointestinal disease. 2. History of motion sickness. 3. Previous history of PONV. 4. Pregnancy or menstruation. 5. Those who had taken anti-emetics within 24 hours before operation. 6. Diabetics. 7. Patients with full stomach. 8. Smokers. 9. History of opioids use.

Design outcomes

Primary

MeasureTime frame
PONV incidence in both the groups.Timepoint: 48 hours

Secondary

MeasureTime frame
1. Serial blood sugar levels 2. Total analgesic requirement in 24 hrs 3. Side effects like headache, dizziness, diarrhea, hypotension, bradycardia if any.Timepoint: 48 hours

Countries

India

Contacts

Public ContactPrashant Dhatwalia

Indira Gandhi Medical College, Shimla, HP

pathaniajyoti7@gmail.com9418120659

Outcome results

None listed

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