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The effects of different doses of oxycodone combined with propofol on hysteroscopy

The effects of different doses of oxycodone combined with propofol on hysteroscopy, A prospective, double blind randomized study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16008895
Enrollment
Unknown
Registered
2016-07-23
Start date
2016-08-01
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

hysteroscopy

Interventions

Sponsors

Wenzhou People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Scheduled for the patients who undergone hysteroscopy, ranging in age from 20 to 52 years old, BMI in 17 ~ 27 kg/m2, ASA I-II

Exclusion criteria

Exclusion criteria: Patients with a history of severity heart and lung diseases, psychiatric disease, allergy or hypersensitivity to local anesthetics and long-term administration of analgesics were excluded.

Design outcomes

Primary

MeasureTime frame
Propofol induced dosage;Propofol maintenance dosage;Propofol total dosage;total propofol use time;the consumption of propofol per hour;operation time;body movement;emergence time;occurrence of adverse cardiovascular events;hypoxemia,;adverse reactions;numeric rating scales;BP;HR;SPO2;

Countries

China

Contacts

Public ContactXianghui Miao

Wenzhou People's Hospital

stonemagical@163.com+86 13968852430

Outcome results

None listed

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