Skip to content

Clinical application of non-constant infusion mode in postoperative analgesia after laparoscopic myomectomy

Clinical application of non-constant infusion mode in postoperative analgesia after laparoscopic myomectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100820
Enrollment
Unknown
Registered
2025-04-15
Start date
2025-04-15
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Uterine fibroids

Interventions

Non-constant background group:Automatic adjustment of background volume infusion
Constant background group:Keep background volume constant infusion

Sponsors

Zhejiang Province Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-70 years old, with a BMI of 18 - 30kg/m^2, planning to undergo laparoscopic myomectomy;2. Clear consciousness, able to communicate normally and understand NRS scores;3. Be able to understand and use PCA analgesia;3. No analgesic drugs were used before surgery;4. No history of drug abuse;5. ASA I-II, willing to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with chronic pain and long-term use of opioid painkillers;2. Patients with a history of neurological, psychiatric, endocrine, renal or liver diseases

Design outcomes

Primary

MeasureTime frame
Nausea and vomiting;

Secondary

MeasureTime frame
Opioid use;Pain score;

Countries

China

Contacts

Public ContactQian Ma

Zhejiang Province Hospital of Traditional Chinese Medicine

maqian459@126.com+86 158 6885 0056

Outcome results

None listed

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