Evaluation of the effect of oxycodone hydrochloride for analgesia after cesarean section: a prospective, double-blind, randomized, controlled trial

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IPR-16008276

Enrollment

Unknown

Registered

2016-04-13

Start date

2016-04-14

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

General surgery

Interventions

A:morphine

B:Oxycodone

Eligibility

Sex/Gender

Female

Age

16 Years to 45 Years

Inclusion criteria

Inclusion criteria: 148 ASA physical status I parturientes at full-term gestation, 18-45 yr of age, at term gestation (longer than 37 weeks) with a singleton uncomplicated pregnancy

Exclusion criteria

Exclusion criteria: Age younger than 16 years, height less than 150 cm or more than 180 cm, weight less than 50 kg or more than 100 kg, bleeding disorders, had hypertension, any hypertensive disease of pregnancy, diabetes mellitus, any contraindication to regional anesthesia, or an allergy to any of the study medications.

Design outcomes

Primary

Measure	Time frame
visual analog scale;	—

Secondary

Measure	Time frame
Total oxycodone consumption;side effect;	—

Countries

China

Contacts

Public ContactZhefeng Quan

Beijing YouAn Hospital, Capital Medial University

15811190059@126.com+86 15811190059

Outcome results

None listed

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