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The Effect of Oxycodone-Directed Analgesic Regimens on Postoperative Nausea and Vomiting in Gynecological Laparoscopy: Risk Factors for Visceral Pain

The Effect of Oxycodone-Directed Analgesic Regimens on Postoperative Nausea and Vomiting in Gynecological Laparoscopy: Risk Factors for Visceral Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113421
Enrollment
Unknown
Registered
2025-11-27
Start date
2025-11-30
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Postoperative nausea and vomiting

Interventions

Oxycodone+Sufentanil group:Oxycodone+Sufentanil

Sponsors

The First Affiliated Hospital of Wannan Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1 Women of reproductive age undergoing gynecological laparoscopic surgery under general anesthesia; 2 Age range 20-60 years.

Exclusion criteria

Exclusion criteria: 1. Patients who use antiemetic drugs for a long time; 2. Patients with other existing conditions that may increase the likelihood of nausea and vomiting (such as a history of motion sickness); 3. Patients with existing neurological or psychiatric disorders; 4. Patients with chronic pain syndrome; 5. Patients who abuse alcohol or drugs

Design outcomes

Primary

MeasureTime frame
The number of times nausea and vomiting occurred within 48 hours after the operation;

Secondary

MeasureTime frame
The incidence of moderate-to-severe pain within 48 hours postoperatively;The incidence of moderate to severe visceral pain within 48 hours after surgery;The incidence of moderate to severe incision pain within 48 hours after the operation;Sedation scores;The number of PCA demands within 48 hours postoperatively;

Countries

China

Contacts

Public ContactGuo Wenjun

The First Affiliated Hospital of Wannan Medical College

Gwj8581@sina.com+86 136 0553 2244

Outcome results

None listed

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