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Comparison of intravenous analgesia load for postoperative analgesia, nausea and vomiting after gynecological laparoscopic surgery: a randomized controlled trial

Comparison of intravenous analgesia load for postoperative analgesia, nausea and vomiting after gynecological laparoscopic surgery: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021408
Enrollment
Unknown
Registered
2019-02-19
Start date
2019-02-20
Completion date
Unknown
Last updated
2019-02-25

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

Conditions

Laparoscopic minimally invasive surgery

Interventions

Group 1:Abdominal transverse fascia block + intravenous patient controlled analgesia
Group 2:Abdominal transverse fascia block + intravenous patient controlled analgesia + load

Sponsors

Affiliated Hospital of Zunyi Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years; 2. BMI 18-28kg / m2; 3. ASA grade I-II level; 4. No serious vision, hearing impairment, readable text 5. Other.

Exclusion criteria

Exclusion criteria: 1. Patients with severe heart, liver and pulmonary dysfunction, who need to continue treatment after ICU; 2. Abnormal blood coagulation function; 3. History of allergic drug anesthesia; 4. Long-term drinking, chronic pain or long-term use of psychotropic drugs; 5. Puncture site Scar, infection, tumor; 6. History of malignant hyperthermia or family history; 7. Pregnant women and lactation; 8. Endocrine disease; 9. Central nausea, vomiting history; 10. Smokers

Design outcomes

Primary

MeasureTime frame
WHO classification criteria for nausea and vomiting;Visual Analog Score;Catecholamine;

Secondary

MeasureTime frame
Basic vital signs;

Countries

China

Contacts

Public ContactLiu Dexing

Affiliated Hospital of Zunyi Medical University, Guizhou Province

pokowenl@163.com+86 18685620143

Outcome results

None listed

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