Comaprsion of effects on induciton and postoperative pain in patients undergoing laparoscopic myomectomy: a randomized controlled double blind trial comparing fentanyl and oxycodone

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IPR-17011085

Enrollment

Unknown

Registered

2017-04-07

Start date

2017-04-04

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

Drug effection

Interventions

oxycodone 1:oxycodone induction dose 0.35mg/kg

oxycodone 2:oxycodone induction dose 0.30mg/kg

Fentanyl :Fentanyl induction dose 5ug/kg

Eligibility

Sex/Gender

Female

Age

18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Adult female aged 18 to 65 years, undergoing laparoscopic myomectomy and subtotal hysterectomy patients, ASA I-II

Exclusion criteria

Exclusion criteria: Excluding serious liver and kidney dysfunction, without controled severe hypertension, severe arrhythmia and sinus tachycardia, and patients taking beta blockers to control heart rate, with chronic pain and taking long-term medication analgesia, and patients taking monoamine oxidase inhibitors and difficult intubation patients.

Design outcomes

Primary

Measure	Time frame
Hemodynamic response of intubation;	—

Secondary

Measure	Time frame
Recovery time and extubation time;Postoperative analgesia;	—

Countries

China

Contacts

Public ContactBao Fangping

the First Affiliated Hospital, College of Medicine, Zhejiang University

baofp.kelly@163.com+8613958105226

Outcome results

None listed

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