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Effect of multimodal analgesia on postoperative recovery within an enhanced recovery pathway after gynecological laparoscopic surgery: a prospective randomized controlled trial

Effect of multimodal analgesia on postoperative recovery within an enhanced recovery pathway after gynecological laparoscopic surgery: a prospective randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026194
Enrollment
Unknown
Registered
2019-09-26
Start date
2019-10-01
Completion date
Unknown
Last updated
2019-09-30

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

Conditions

gynecological laparoscopic surgery

Interventions

ERAS Group:multimodal analgesia
Control group:routine analgesia

Sponsors

Department of Anesthesiology, Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Aged 18 to 65 years, American Society of Anesthesiologists(ASA) I-II, scheduled to undergo elective gynecological laparoscopic surgery, informed consent was signed.

Exclusion criteria

Exclusion criteria: Patient with history of gastrointestinal ulcer, gastrointestinal bleeding or perforation, epilepsy. History of asthma, urticaria or allergic reaction after taking aspirin or other NSAID drugs. Liver or renal insufficiency. Allergies to acetaminophen, NSAID, sulfonamide and floxacin, patients with monoamine oxidase inhibitors, dicoumarin anticoagulants, selective serotonin reuptake inhibitors preoperatively, pregnant or breast-feeding patients.

Design outcomes

Primary

MeasureTime frame
QoR-40 score;—

Countries

China

Contacts

Public ContactZhiyu Geng

Department of Anesthesiology, Peking University First Hospital

gengzhiyu2013@163.com+86 010-83573218

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 22, 2026